Abstract
Background/Objectives: This scoping review critically evaluated existing literature and summarized the impact of occupational, physiological, and psychological stressors on adrenal and neuroendocrine responses, body composition, and physical performance amongst women in tactical occupations. Methods: Boolean searches identified potentially qualifying reports involving: (1) adult women (≥19 y) currently employed or completing their training for a tactical profession; (2) ≥1 marker of “stress”; and (3) ≥1 adrenal, neuroendocrine, body composition, or fitness/performance outcome. Quantitative data (e.g., sample characteristics, outcomes of interest) were extracted and summarized. The completeness of reporting for each study was documented using existing checklists and quantified as: low (<50%), moderate (50–79%), or high (≥80%). Results: 40 studies (k) of moderate reporting quality (~64%) were included in the final sample (3693 women); 11 studies (28%) focused on women exclusively, and 16 studies identified sex differences in ≥1 outcome. Most studies involved military trainee populations (80%, k = 32). Occupation-related stress tended to negatively impact adrenal, neuroendocrine, body composition, and performance outcomes. Conclusions: This review highlights progress in assessing occupational performance in female tactical personnel exposed to diverse stressors; however, our understanding remains incomplete due to methodological and conceptual limitations in the literature. Holistic research strategies are needed to capture the complexity of performance readiness in women, integrating how stress affects key tactical performance aspects such as muscle physiology, reproductive health, and energy and nutrient balance in realistic operational contexts. Integrating such data is vital for informing policy, improving readiness, and enhancing the health and career longevity of female tactical personnel.
Keywords: women, stress, tactical athletes, body composition, exercise performance, tactical occupations, scoping review
1. Introduction
Women now represent approximately 9–20% of the workforce in tactical professions, including military, law enforcement, firefighting, emergency medical services (EMS), and corrections [1,2]. Women’s expanding presence in physically and psychologically demanding tactical occupational roles has prompted a growing need to better understand the unique physiological and performance-related demands placed on women in these environments. In the United States (U.S.), women now serve across all branches of the military, including previously restricted combat arms roles, and are eligible for selection into elite units (e.g., Infantry, Special Forces) [3]. In other tactical sectors such as law enforcement and wildland firefighting, women have served for decades, though their representation and access to specialized teams (e.g., Special Weapons and Tactics unit) remain variable across jurisdictions. Internationally, women serve in both volunteer and conscripted forces, with some integrated into combat arms units [4]. Despite advancements in access and representation, critical gaps persist in understanding the physiological, psychological, and occupational implications of tactical service for women.
Tactical professions are characterized by high physiological demands, including heavy load carriage [5,6,7], environmental exposures (e.g., heat, cold, smoke, high altitude) [8,9,10,11], prolonged operational stress [12,13,14], and disrupted sleep and circadian rhythms [14,15]. These are further compounded by psychosocial challenges, including exposure to trauma [14,16], underrepresentation in male-dominated units, and elevated risk for gender-specific stressors such as sexual harassment or assault [17,18,19]. This stress may accumulate over years of service (i.e., chronic) or may result from short-term events (i.e., acute) such as high-intensity training programs or brief, demanding operations (e.g., Basic Combat Training, disaster response scenarios). Tactical training and occupational stress have systemic physiological impacts and may negatively impact readiness and performance. The cumulative impact of occupational stressors (i.e., allostatic load) and the interconnected nature of systemic effects can lead to outcomes such as an overdriven adrenal and neuroendocrine system, worsening cardiometabolic health and body composition profiles, and undesirable changes in physical performance. This combination of outcomes has the potential to negatively influence occupation-specific task performance (Figure 1).
Figure 1.
Relationships (identified through arrows) between acute and chronic stressors and their potential impacts on adrenal and neuroendocrine responses, body composition, and physical performance. The cumulative impact of occupational stressors (i.e., allostatic load) and the inter-connected nature of systemic effects can lead to outcomes such as an overdriven adrenal and neuroendocrine system, worsening cardiometabolic health and body composition profiles, and undesirable changes in physical performance. This image was created using BioRender.com (https://BioRender.com), Procreate® (version 5.3.15), and PowerPoint (version 2.98.4).
The adrenal stress response (Figure 1) refer to the physiological adaptation relative to imposed stress (i.e., adaptation to imposed demands) [20]. The adaptive response to imposed demands serves specific physiological purposes, for example, mobilization of energy stores, delivery of oxygenated blood to metabolically-active tissues, and activation of contractile tissue (i.e., skeletal muscle). Core components of the physiological stress response are the hypothalamus and adrenal glands. The hypothalamic–pituitary (HPA) axis governs the synthesis and secretion of the stress hormone cortisol from the adrenal cortex, while sympathetic nervous system signaling stimulates the adrenal medulla to release catecholamines into circulation as part of the stress response. The magnitude of response to an imposed stressor is relative to the magnitude and duration of demand, regardless of the nature of the stressor (e.g., environmental exposure, physical exertion, occupational demand). Likewise, combined stressors (e.g., intense training bouts, energy deficit, sleep deprivation, psychological stress) have a cumulative impact on the magnitude of stress response [21,22]. Therefore, it follows that tactical occupational demands place a significant adaptation demand on human physiology.
Previous works have established sex differences in stress reactivity, with women initiating HPA axis activity more rapidly, leading to a heightened stress response [23]. This, coupled with sex differences in neuromuscular performance [24,25] and energy metabolism, likely impacts downstream health and performance outcomes [21], prompting notable consequences in tactical settings and thus, a need for more female tactical athlete-focused research. Current tactical training and nutrition recommendations aimed at supporting physical readiness include some female-specific guidelines but have been primarily established through a male-focused lens [26]. Occupational policies and physical training practices have not always adequately addressed, or fully appreciated, the interconnectedness between stress physiology and female-focused factors such as musculoskeletal health and body composition, reproductive health, and physical performance outcomes; each of which includes considerations that impact physical and occupational readiness.
Although the body of research on women in tactical roles is growing, it remains disproportionately focused on male populations [27]. Women’s needs relative to the tactical profession are not fully understood, and little is known about how women’s unique physiological characteristics influence their responses to stress, injury risk, recovery, and long-term performance in these professions. Key areas directly related to tactical performance, such as adrenal stress response, neuroendocrine adaptation, metabolic and skeletal muscle health, and occupational performance under load or fatigue, remain largely underexamined in female cohorts. This knowledge gap offers an opportunity to explore the relationship between tactical stress and readiness, with the intent of using this newly gained knowledge to build targeted tactical health and performance programs that incorporate women-specific considerations.
Thus, the purpose of this scoping review is to synthesize the current literature on women in tactical occupations, with a focused analysis of three interrelated domains: adrenal stress and neuroendocrine responses to occupational stressors, important metabolic health indicators (e.g., body composition), and physical and occupational performance outcomes across training, field operations, and simulated environments. The objectives of this scoping review are to (1) provide a comprehensive overview of the research examining women’s physiological responses and occupational performance to stressful environments in tactical professions; (2) identify key areas of consensus, as well as critical gaps in the literature that hinder effective policy and program development, and (3) offer evidence-informed recommendations for future research and operational readiness and performance optimization strategies that address the specific needs of women in these demanding roles. As more women enter and advance within tactical professions, it is essential to generate sex-specific data that informs occupational health, readiness standards, and long-term career sustainability. This scoping review aims to serve as a foundation in support of these efforts.
2. Materials and Methods
We performed a scoping review in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) Statement [28]. Institutional review board approval was not required for this study since it is a review of existing literature and is not considered intervention research involving humans. The protocol for this scoping review was developed and revised by the research team and is available from the corresponding author upon request.
2.1. Inclusion Criteria
Studies were eligible for inclusion if they satisfied four pre-established inclusion criteria: (1) involved adult participants (≥19 y) that were currently employed in a tactical profession (e.g., military, police, firefighter, emergency medical services) or completing their training for employment (e.g., recruits or cadets); (2) included all women samples or mixed sample where women are analyzed/reported separately; (3) examined at least one marker of “stress”—broadly (i.e., physiological, neuroendocrine, psychological, or occupational stress or strain) or specifically (i.e., blood biomarker, such as circulating epinephrine) defined; and (4) measured at least one outcome related to body composition (e.g., lean mass, fat free mass, or muscle mass; body fat [BF], fat mass, or adiposity) or physical fitness and performance (e.g., fitness test or occupational-specific task).
2.2. Search Strategy
Potential qualifying reports were identified and retrieved from PubMed, EMBASE (via Scopus), and Web of Science using a Boolean search strategy using terms related to “tactical athlete” or “tactical occupation” and outcomes related to stress, body composition, physical fitness, and performance. Searches were not restricted by language, and databases were searched from their inception or earliest coverage date through 26 February 2025. The full search strategy for each electronic database is provided in Table S1 in the Supplementary Materials. Reference lists of included studies, relevant reviews, and meta-analyses were manually searched for additional reports.
Our electronic and manual search methods yielded 667 potentially qualifying reports. After removing duplicates, 534 records remained and were reviewed for inclusion by two authors (EAS, HVM); 102 reports were retrieved for full review. Figure 2 details the search and selection process undertaken for this review.
Figure 2.
Flow chart detailing the search for potential reports (n) and selection process of included studies (k). a Rayyan.ai was used to identify potentially ineligible records during the screening process only. No records were excluded using automation tools, as all were performed by humans (EAS, HVM).
2.3. Data Extraction
Variables of interest were extracted and summarized by major outcomes of interest: adrenal stress and neuroendocrine responses; metabolic health (e.g., body composition, muscle mass); physical fitness and occupational performance. Coded variables include: (1) characteristics of the study, sample, and intervention/exposure (if applicable); (2) the outcomes analyzed and relevant methodology employed; (3) study data, expressed as mean ± standard deviation (SD) (or other quantitative summary), extracted directly from the study, denoting sex differences (whenever possible); and (4) a brief summary regarding the impact of stress and sex on the outcome of interest. Data extraction was performed by one member of the research team (EAS) and checked by a second member (HVM). All disagreements were resolved by discussion.
2.4. Critical Appraisal of Individual Sources of Evidence
A critical appraisal of the studies included in our scoping review was performed to gauge the completeness of reporting (i.e., reporting quality) using the STROBE Checklist for observational, cross-sectional, and cohort studies (95% of our sample) [29] and the CONSORT Checklist for studies with an interventional design (5% of our sample) [30]. Of note, the sole intervention study [31] was not a randomized trial; therefore, the CONSORT checklist was modified, such that questions pertaining to randomization were omitted. For each checklist, we generated an overall score to reflect reporting completeness, which was gauged as a percentage of items satisfied. We used the following thresholds, based on the distribution of scores in our sample using quartiles, to interpret reporting quality scores: low (<50% of items satisfied, quartile 1), moderate (50–79% of items satisfied, quartiles 2 and 3), or high (≥80% of items satisfied, quartile 4), respectively. Reporting quality scores for each study are provided within the summary tables for each outcome of interest.
3. Results
Of the 534 potentially eligible reports identified (after removing duplicates), 104 were obtained for full-text review (102 from electronic searches; 2 from other methods) and independently evaluated by two members of the research team (EAS, HVM), revealing a final sample of 40 studies (k) that satisfied inclusion criteria [22,24,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69]. Figure 2 shows the systematic search for potential reports and the selection process of included studies. More than half of potentially eligible reports (56%; k = 36) were deemed ineligible during full-text review because they failed to disaggregate data by sex. The 64 studies that were excluded following full-text review are summarized in Table S2 as part of the Supplementary Materials.
The majority (80%) of studies in this scoping review focused on military populations; only eight studies (20% of our sample) included police, firefighting, or EMS professions [35,40,41,50]. Twenty-four studies examined two or more outcomes of interest [24,34,36,37,38,40,41]; of these, only five studies evaluated all three of our major outcomes of interest [22,33,55,56,68]. Eleven studies (28%) focused on women exclusively; of the 29 studies with mixed samples, only half (55%; k = 16) evaluated sex differences, and 14 studies found significant differences in one or more outcomes [24,31,34,35,37,38,41,43,49,54,56,57,59,68,69].
Overall, our review summarizes data from 3693 women, most of whom were recruits or cadets (87%). Studies that included servicewomen (k = 12), reported ~8 years (y) of service, although this ranged from 3 to 14 y. See Table 1 for a summary of included studies in the total sample and by tactical occupation. Table 2, Table 3 and Table 4 summarize the coded dimensions for each of the studies included in this review, grouped by the major outcomes of interest.
Table 1.
Summary of included studies for the total sample and by tactical occupation.
| Total (k = 40) N = 3693 |
Military (k = 32) n = 2702 |
Police (k = 6) n = 864 |
EMS (k = 1) n = 28 |
Fire (k = 1) n = 3 |
||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| k | M | SD | Min, Max | k | M | SD | Min, Max | k | M | SD | Min, Max | k | M | SD | Min, Max | k | M | SD | Min, Max | |
| Age (y) | 38 | 26.9 | 7.5 | 18.8, 47.6 | 30 | 24.4 | 5.4 | 18.8, 44.1 | 6 | 35.6 | 4.4 | 27.5, 39.6 | 1 | 47.6 | 9.4 | - | 1 | 26 | 3 | - |
| Recruits/ Cadets, n (%) |
28 | 3228 | 87.4% | 24 | 1917 | 70.9% | 1 | 682 | 78.9% | 0 | 0 | 0% | 0 | 0 | 0% | |||||
| Servicewomen, n (%) | 12 | 953 | 25.8% | 3 | 673 | 24.9% | 4 | 249 | 28.8% | 1 | 28 | 100% | 1 | 3 | 100% | |||||
| Service (y) | 6 | 8.2 | 4.1 | 3.0, 14.1 | 2 | 3.2 | 0.2 | 3.0, 3.3 | 4 | 9.8 | 2.4 | 7.4, 13.1 | 1 | 14.1 | 8.2 | - | 1 | 6 | 2 | - |
| Body mass (kg) | 31 | 67.1 | 5.6 | 60.9, 82.3 | 33 | 66.8 | 5.6 | 60.9, 82.3 | 3 | 72.2 | 6.2 | 67.8, 76.5 | - | 1 | 66.7 | 4.4 | - | |||
| BF (%) | 14 | 28.3 | 4.9 | 17.2, 36.0 | 13 | 27.9 | 4.8 | 17.2, 36.0 | 1 | 33.7 | - | - | - | |||||||
| BMI (kg/m2) | 26 | 25.1 | 2.1 | 22.4, 30.2 | 25 | 25.1 | 2.1 | 22.4, 30.2 | 6 | 25.4 | 2.2 | 23.0, 28.0 | - | 1 | 24.3 | 1.7 | - | |||
| WC (cm) | 2 | 76.0 | 6.3 | 71.5, 80.4 | 1 | 71.5 | - | 1 | 80.4 | - | - | - | ||||||||
| VO2max (mL/kg/min) | 9 | 36.0 | 4.3 | 27.2, 40.5 | 6 | 36.5 | 7.0 | 32.5, 40.5 | 3 | 35.2 | 7.0 | 27.2, 40.4 | - | - | ||||||
BF, Body fat. BMI, Body mass index. EMS, Emergency medical services. k, Number of studies. M, mean. Max, Maximum. Min, Minimum. N, Total number of women included in the scoping review. n, Number of women included in the scoping review within the tactical domain. SD, Standard deviation. VO2max, Maximal oxygen uptake. WC, Waist circumference.
Table 2.
Summary of the studies included in the scoping review that evaluated adrenal stress and neuroendocrine responses.
| Author, Year |
Tactical Domain and Study Characteristics | Sample Characteristics | Adrenal and Neuroendocrine Responses | Other Markers Analyzed |
Impact of Stress and Sex on Adrenal and Neuroendocrine Responses | |
|---|---|---|---|---|---|---|
| Outcomes and Assessment Details |
Aggregate-Level Study Data (Mean ± SD) a |
|||||
| Andrews et al., 2010 † [33] RQ: 51.6% |
Military Design: Cross-sectional; service members completing the Army Physical Fitness Test (Washington, DC, USA) Primary outcomes: Oxidative stress |
|
Oxidative stress biomarkers: Creatine kinase, C-reactive protein, glutathione peroxidase, superoxide dismutase Methods: Serum (Creatine kinase and C-reactive protein) and plasma (glutathione peroxidase and superoxide dismutase) Fasted status: NR |
Creatine kinase, U/L (F): Pre (n = 18): 117.0 ± 57.3 Post (n = 17): 153.9 ± 63.5 Post 24 h (n = 7): 169.0 ± 70.2 * C-reactive protein, mg/dL (F): Pre (n = 17): 0.29 ± 0.28 Post (n = 14): 0.29 ± 0.23 Post 24 h (n = 7): 0.34 ± 0.27 Glutathione peroxidase, ng/dL (F): Pre (n = 17): 76.2 ± 42.0 Post (n = 17): 70.8 ± 29.3 Superoxide dismutase, ng/dL (F): Pre (n = 16): 0.80 ± 0.62 Post (n = 16): 0.95 ± 0.63 * p < 0.05 (time) |
Baseline: Body composition, fitness level, dietary intake |
|
| Cho et al., 2017 [36] RQ: 42.4% |
Military Design: Prospective cohort (8 wk); during 16-wk Officer training course at the Korea Third Military Academy (Yeongcheon, South Korea) Primary outcomes: Reproductive function |
|
Hormones: Cortisol, CRH, estradiol Methods: Serum Fasted status: Overnight |
Cortisol, μg/dL: Baseline: 16.1 ± 3.9 Wk 4: 18.1 ± 2.2 Wk 8: 18.7 ± 2.2 * CRH, pg/dL: Baseline: 84.4 ± 65.1 Wk 4: 57.7 ± 28.3 Wk 8: 22.0 ± 21.7 * Estradiol, pg/dL: Baseline: 106.0 ± 120.7 Wk 4: 44.6 ± 24.4 Wk 8: 55.1 ± 43.1 * * p < 0.01 (time) |
Reproductive function: regularity, prolactin, endorphin-β, NPY, leptin, orexin-A, ghrelin, follicle-stimulating hormone, luteinizing hormone, thyroid-stimulating hormone, thyroxine |
|
| Conkright et al., 2021 ‡ [24] RQ: 57.6% |
Military Design: Prospective cohort; 5-day simulated military operational stress protocol (Pittsburgh, PA, USA) Primary outcomes: Neuromuscular performance, mood state, and hormonal responses |
|
Hormones: Cortisol, IGF-1 Methods: Serum (PRE and POST tactical mobility test) Fasted status: Overnight |
Cortisol, μg/dL (PRE) (F): Day 1: 14.4 ± 3.8 Day 3: 12.6 ± 4.7 Day 4: 12.7 ± 4.3 Cortisol, μg/dL (POST) (F): Day 1: 23.5 ± 5.7 * Day 3: 26.8 ± 6.5 * Day 4: 25.1 ± 9.2 * IGF-1, ng/mL (PRE) (F): Day 1: 409.3 ± 118.9 Day 3: 353.1 ± 93.3 Day 4: 321.7 ± 95.8 IGF-1, ng/mL (POST) (F): Day 1: 397.7 ± 93.3 Day 3: 360.6 ± 108.1 * Day 4: 335.8 ± 98.2 *,** * p < 0.05 (time, POST vs. PRE), ** p < 0.05 (day) |
Neuromuscular performance: Lower body power, tactical mobility test Mood state: POMS subscales (tension, depression, anger, fatigue, confusion, vigor) Other hormones: Growth hormone, brain-derived neurotrophic factor |
|
| Flegr et al., 2012 [43] RQ: 43.8% |
Military Design: Cross-sectional; psychological performance battery as part of entrance examination (Central Military Hospital, Prague, Czech Republic) Primary outcomes: Psychological health and performance, hormones |
|
Hormones: Cortisol, testosterone, estradiol Methods: Serum Fasted status: NR |
Cortisol, nmol/L (F): 728 ± 121 * Testosterone, nmol/L (F): 1.10 ± 3.87 * Estradiol, nmol/L (F): 0.29 ± 0.03 * * p < 0.001 (sex) |
Psychological health: Questionnaires (N-70, OD-1, Buss–Dürker Inventory) Psychological performance: Meili selective memory test, TOPP test (attention and short-term memory), Wiener Matrizen-Test, OTIS test (verbal intelligence) |
|
| Gifford et al., 2019 ‡ [44] RQ: 78.8% |
Military Design: Prospective cohort (11 months); Commissioning Course (infantry-based training) at the Royal Military Academy (Sandhurst, UK) Primary outcomes: HPA axis function, mental health Part of the Female Endocrinology in Arduous Training (FEAT) Study |
|
Hormones: Cortisol Methods: HCC and salivary cortisol (measured AM and PM), plasma cortisol (measured in AM, separated into non-CCP vs. CCP users) Fasted status: Overnight (plasma only) |
HCC, pg/mg (ln): Month 1: 2.0 ± 0.9 * Month 2: 2.1 ± 0.8 * Month 3: 2.1 ± 1.0 * Month 4: 2.0 ± 1.1 * Month 5: 2.0 ± 0.9 Month 6: 2.2 ± 0.7 Month 7: 2.2 ± 0.9 Month 8: 2.1 ± 0.9 Month 9: 2.2 ± 0.9 * Month 10: 2.4 ± 0.9 * Month 11: 2.4 ± 0.7 * Month 12: 2.2 ± 0.9 * Cortisol (saliva), μg/dL ** T1: Wk 1 = 0.4 ± 0.3, Wk 7 = 0.6 ± 0.2, Wk 14 = 0.5 ± 0.3 T2: Wk 1 = 0.6 ± 0.3, Wk 5 = 0.5 ± 0.1, Wk 14 = 0.4 ± 0.3 T3: Wk 1 = 0.5 ± 0.2, Wk 5 = 0.5 ± 0.2, Wk 14 = 0.4 ± 0.2 Cortisol (plasma), nmol/L: non-CCP users ** T1: Wk 1 = 701.0 ± 134.6 T2: Wk 14 = 669.3 ± 162.4 T3: Wk 13 = 558.4 ± 182.2 CCP users ** T1: Wk 1 = 1061.4 ± 198.0 T2: Wk 14 = 966.3 ± 166.4 T3 Wk 13 = 855.4 ± 190.1 * p < 0.05 (time, vs. pre-6 to pre-4), ** p < 0.001 (main effect, time) |
Mental health: Anxiety, depression, resilience |
|
| Gifford et al., 2025 ‡ [46] RQ: 72.7% |
Military Design: Prospective cohort (11 months); Commissioning Course (infantry-based training) at the Royal Military Academy (Sandhurst, UK) Primary outcomes: HPA axis function, HPG axis function Part of the Female Endocrinology in Arduous Training (FEAT) Study |
|
Hormones: Cortisol Methods: HCC, saliva, plasma (in response to 1 μL ACTH over 1 h) Fasted status: Overnight (plasma) |
Ln-HCC, pg/mg (F): Month 0: 2.1 (0.2) Month 1: 2.3 (0.1) Month 2: 2.1 (0.2) Month 3: 2.0 (0.2) Month 4: 1.8 (0.2) Month 5: 2.1 (0.2) * Month 6: 2.2 (0.1) * Month 7: 2.0 (0.2) * Month 8: 2.2 (0.2) Month 9: 2.3 (0.2) * Month 10: 2.4 (0.2) * Month 11: 2.1 (0.2) * Cortisol, μg/dL—saliva (F): Wk 1: AM = 0.45 (0.06) vs. PM = 0.11 (0.01) Wk 8: AM = 0.62 (0.05) * vs. PM = 0.09 (0.03) Wk 14: AM = 0.55 (0.05) vs. PM = 0.09 (0.02) Wk 16: AM = 0.58 (0.06) vs. PM = 0.09 (0.02) Wk 20: AM = 0.47 (0.04) * vs. PM = 0.11 (0.03) Wk 29: AM = 0.44 (0.05) vs. PM = 0.15 (0.03) Cortisol, nmol/L—plasma (F) * Wk 1 Min 0: 197.0 (24.1) Wk 29 Min 0: 255.6 (53.0) Wk 1 Min 20: 512.1 (27.9) Wk 29 Min 20: 574.1 (23.4) Wk 1 Min 30: 564.2 (35.5) Wk 29 Min 30: 672.2 (25.9) Wk 1 Min 40: 532.4 (35.6) Wk 29 Min 40: 540.7 (18.6) Wk 1 Min 60: 466.3 (30.5) Wk 29 Min 60: 479.0 (18.5) * p < 0.05 (sex × time) |
Other hormones: Gonadotrophins (follicle-stimulating hormone, gonadotrophin-releasing hormone, luteinizing hormone) |
|
| Johnsen et al., 2023 [48] RQ: 71.9% |
Emergency medical services Design: Cross-sectional Primary outcomes: Physiological and psychosocial stress |
|
Hormones: Cortisol Methods: HCC Fasted status: NR |
Cortisol, pg/mg (F): 23.5 [IQR: 11.6–47.0] p = 0.719 (sex) |
Psychosocial stress: 17-item Demand–Control–Support Questionnaire |
|
| Lieberman et al., 2008 [51] RQ: 66.7% |
Military Design: Prospective cohort (13 wk); U.S. Marine Corps basic training (Parris Island, SC, USA) Primary outcomes: Body composition, metabolic status, mood state |
|
Hormones: Cortisol Methods: Serum Fasted status: Overnight |
Cortisol, μg/dL: Wk 1: 13.2 ± 0.7 Wk 12: 10.4 ± 0.7 p < 0.003 (time) |
Body composition: BM, FM, FFM, BF, BMM Metabolic status: Cholesterol (total, LDL, HDL), free fatty acids, glucose Mood state: POMS subscales (fatigue, confusion, depression, tension, anger, vigor) |
|
| Lieberman et al., 2012 [52] RQ: 60.6% |
Military Design: Prospective cohort (12 wk); U.S. Marine Corps basic training (Parris Island, SC, USA) Primary outcomes: Body composition, mood state, metabolic status |
|
Hormones: ACTH Methods: Serum Fasted status: Overnight |
ACTH, pg/mL: Pre: 16.2 ± 9.7 Post: 15.4 ± 8.0 p = 0.583 (time) |
Body composition: BM, FM, LM, BMM Mood state: POMS subscales (fatigue, confusion, depression, tension, anger, vigor) Metabolic status: Substance P, fructosamine, cholesterol (total, HDL, LDL), triglycerides, free fatty acids, DHEA-S |
|
| McFadden et al., 2024a ‡ [54] RQ: 72.7% |
Military Design: Prospective cohort (13 wk); U.S. Marine Corps basic training (Parris Island, SC, USA) Primary outcomes: Sex differences in workload, sleep, stress, and performance Part of a larger study, the U.S. Marine Corps Gender-Integrated Recruit Training study |
|
Hormones: Cortisol Methods: Saliva Fasted status: NR |
Cortisol, μg/dL: Wk 2: 0.78 (0.03) Wk 7/8: 0.63 (0.02) Wk 11: 0.77 (0.07) p = 0.01 (sex × time) |
Performance: Lower body strength and power Workload: Relative energy expenditure, distance, steps Sleep: Continuity and duration |
|
| McFadden et al., 2024b [55] RQ: 72.7% |
Military Design: Prospective cohort (11 wk); U.S. Marine Corps basic training (Parris Island, SC, USA) Primary outcomes: Performance, resilience, wearable tracking Part of a larger study, the U.S. Marine Corps Gender-Integrated Recruit Training study |
|
Hormones: Cortisol Methods: Saliva Fasted status: NR |
Cortisol, μg/dL: Wk 2: 0.8 ± 0.4 Wk 7: 0.6 ± 0.3 Wk 11: 0.8 ± 0.7 p-value NR |
Performance: U.S. Marine Corps—specific performance, lower body strength, and power Resilience: Connor–Davidson Resilience Scale, workload, self-reported sleep, stress Wearable tracking: energy expenditure, distances, sleep, acceleration |
|
| McGraw et al., 2013 † [31] RQ: 64.3% |
Military Design: Quasi-experimental (within-subjects, repeated measures); 10-min combat casualty simulation Primary outcomes: Biological reactivity |
|
Hormones: Cortisol, α-amylase Cardiovascular: HR, SBP, DBP Methods: Saliva (cortisol, α-amylase); measured at baseline (−20 min), immediately pre-simulation (−5 min), midway simulation (+5 min), post-simulation (+10 min), and during recovery (+20 min and +40 min) Fasted status: NR |
Cortisol, μg/dL (F): Baseline (−20 min): 0.2 ± 0.1 Pre (−5 min): 0.2 ± 0.1 Mid (+5 min): 0.2 ± 0.1 * Post (+10 min): NR Post 2 (+20 min): 0.2 ± 0.1 * Post 3 (+40 min): 0.2 ± 0.1 * α-amylase, U/mL (F): Baseline (−20 min): 122.1 ± 69.7 Pre (−5 min): 136.6 ± 82.4 * Mid (+5 min): 193.1 ± 142.9 * Post (+10 min): NR Post 2 (+20 min): 141.3 ± 120.6 Post 3 (+40 min): 117.7 ± 91.5 HR, beats/min (F): Baseline (−20 min): 78.9 ± 13.7 Pre (−5 min): 81.6 ± 15.3 * Mid (+5 min): 126.9 ± 18.3 * Post (+10 min): 89.9 ± 17.1 Post 2 (+20 min): 84.9 ± 13.4 Post 3 (+40 min): 76.6 ± 12.8 SBP, mmHg (F): Baseline (−20 min): 116.0 ± 11.0 Pre (−5 min): 128.1 ± 12.7 * Mid (+5 min): NR Post (+10 min): 128.6 ± 11.4 Post 2 (+20 min): 118.6 ± 11.2 Post 3 (+40 min): 115.9 ± 10.3 DBP, mmHg (F): Baseline (−20 min): 74.5 ± 8.5 Pre (−5 min): 80.2 ± 8.4 * Mid (+5 min): NR Post (+10 min): 81.7 ± 7.9 Post 2 (+20 min): 76.0 ± 8.4 Post 3 (+40 min): 73.9 ± 9.3 * p < 0.01 (time, vs. baseline) |
None |
|
| Nindl et al., 2012 [56] RQ: 57.6% |
Military Design: Prospective cohort (~4 months); Israeli Defense Force gender-integrated basic recruit training program (Tel Hashomer, Israel) Primary outcomes: Body composition, inflammation, fitness |
|
Hormones: IGF-1, free IGF-1 Methods: Serum Fasted status: Overnight |
IGF-1 (F): Pre: 470.0 (15.8) ng/mL Post: 524.6 (15.3) ng/mL p > 0.05 (sex) p < 0.05 (time) Free IGF-1 (F): Pre: 0.49 (0.04) ng/mL Post: 0.52 (0.05) ng/mL p > 0.05 (Sex) p > 0.05 (Time) |
Body composition: BM, FM, FFM, BF Inflammation: IL-1β, IL-6, TNF-α, IGFBP-1, IGFBP-2, IGFBP-3, IGFBP-4, IGFBP-5, IGFBP-6 |
|
| O’Leary et al., 2023 †,‡ [59] RQ: 87.9% |
Military Design: Prospective cohort (36 h); field exercise in energy deficit as part of Commissioning Course at the Royal Military Academy (Sandhurst, UK) Primary outcomes: Bone turnover, diet, energy expenditure |
|
Hormones: Cortisol, testosterone Methods: Plasma Fasted status: Overnight |
Cortisol, nmol/L: Baseline: 650.8 ± 229.9 Post: 578.5 ± 219.5 Recovery: 606.9 ± 165.3 p > 0.05 (time) Testosterone, nmol/L: Baseline: 1.4 ± 1.2 Post: 0.8 ± 0.5 Recovery: 0.8 ± 0.3 p > 0.05 (time) |
Bone turnover: βCTX, PINP, parathyroid hormone, total 25(OH)D, albumin-adjusted calcium, total 1,25(OH)2D, phosphate, total 24,25(OH)2D Diet: carbohydrate, protein, and fat intake Energetics: energy expenditure and balance (accelerometry and doubly labeled water) |
|
| O’Leary et al., 2024 ‡ [60] RQ: 66.7% |
Military Design: Prospective cohort (44 wk); Commissioning Course (basic combat training program) at the Royal Military Academy (Sandhurst, UK) Primary outcomes: Energy balance, bone turnover, metabolic and endocrine statuses |
|
Hormones: Cortisol, IGF-1, testosterone Methods: Plasma (cortisol, testosterone) and serum (IGF-1) Fasted status: Overnight |
Cortisol, nmoll/L (F) * Baseline: 776.3 ± 174.6 Term 2: 724.3 ± 226.6 Term 3: 733.6 ± 202.4 IGF-1, nmmol/L (F) Baseline: 215.5 ± 52.5 Term 2: 230.4 ± 65.2 Term 3: 233.7 ± 52.7 Testosterone, nmoll/L (F) * Baseline: 0.7 ± 0.2 Term 2: 0.7 ± 0.3 Term 3: 1.2 ± 1.5 * p < 0.05 (time) |
Body composition: LM, FM, BF Energetics: energy intake, energy balance, energy expenditure, macronutrient intake Bone turnover: Bone alkaline phosphatase, βCTX, PINP Metabolic and endocrine statuses: Leptin, triiodothyronine, free thyroxine, thyroid-stimulating hormone, sex hormone-binding globulin, free androgen index |
|
| Strahler et al., 2015 ‡ [65] RQ: 65.6% |
Police Design: Cross-sectional; simulated school shooting exercise as part of basic or refresher training session Primary outcomes: Psychobiological stress |
|
Hormones: α-amylase Methods: Saliva Fasted status: NR |
α-amylase, U/mL (F): Basal: 125.8 (26.6) +1 min: 259.2 (69.2) +20 min: 199.7 (40.4) +40 min: 218.2 (32.9) p-value NR |
Psychological state: Chronic and acute stress, mood Physiological stress: Cortisol, HR, HR variability (only α-amylase data were disaggregated by sex) |
|
| Szivak et al., 2018 †,# [22] RQ: 65.6% |
Military Design: Prospective cohort (2 wk); U.S. Navy SERE training (Kittery and Rangeley, ME, USA) Primary outcomes: Neuroendocrine markers and performance |
|
Hormones: Epinephrine, norepinephrine, dopamine, cortisol, testosterone, NPY Methods: Serum (cortisol, testosterone), plasma (NPY, epinephrine, norepinephrine, dopamine) Fasted status: Yes (time-period not specified) |
Cortisol, nmol/L (F): Baseline: 139.8 ± 60.6 Stress: 937.4 ± 276.4 Recovery: 251.1 ± 60.5 Testosterone, nmol/L (F): Baseline: 1.1 ± 0.2 Stress: 1.8 ± 0.3 Recovery: 1.0 ± 0.2 NPY, pg/mL (F): Baseline: 356.7 ± 53.5 Stress: 317.3 ± 92.2 Recovery: 174.3 ± 26.6 Epinephrine, pmol/L (F): Baseline: 234.7 ± 88.8 Stress: 361.6 ± 155.5 Recovery: 182.8 ± 82.3 Norepinephrine, pmol/L (F): Baseline: 2291.5 ± 360.0 Stress: 6511.0 ± 2089.6 Recovery: 3855.5 ± 1267.4 Dopamine, pmol/L (F): Baseline: 87.0 ± 13.3 Stress: 169.6 ± 36.0 Recovery: 133.7 ± 30.8 p-values: NR for all outcomes |
Physical performance: Dominant handgrip strength, vertical jump height |
|
| Tomei et al., 2008 [67] RQ: 34.4% |
Police Design: Cross-sectional; urban stressor exposure (Rome, Italy) Primary outcomes: Testosterone |
|
Hormones: Free testosterone Methods: Plasma Fasted status: Overnight |
Free testosterone, pg/mL: Baseline: 1.4 ± 0.6 p < 0.001 (control) |
None |
|
| Vikmoen et al., 2020 † [68] RQ: 63.6% |
Military Design: Prospective cohort (14 days) during a 6-day field-based Selection Exercise at Rena Military Camp (Rena, Norway) Primary outcomes: Body composition and performance |
|
Hormones: Cortisol, IGF-1, testosterone Methods: Serum Fasted status: Overnight |
Cortisol, ug/dL (F): Pre: 343 ± 219 Post 24 h: 771 ± 155 * Post 72 h: 677 ± 196 * Post 1 wk: 666 ± 101 * Post 2 wk: 711 ± 82 * IGF-1, nmol/L (F): Pre: 17.6 ± 5.1 Post 24 h: 10.1 ± 2.6 * Post 72 h: 13.7 ± 4.3 * Post 1 wk: 23.7 ± 6.9 * Post 2 wk: 26.8 ± 7.9 * Testosterone, nmol/L (F): Pre: 1.0 ± 0.5 Post 24 h: 1.2 ± 0.4 Post 72 h: 1.1 ± 0.4 Post 1 wk: 1.1 ± 0.3 Post 2 wk: 1.0 ± 0.3 * p < 0.05 (time, vs. pre) |
Body composition: BM, MM, FM Performance: CMJ height and maximal power, medicine ball throw, anaerobic performance (Evacuation test) Other: Creatine kinase |
|
a Summarized as mean ± standard deviation (SD), mean (standard error), or median [interquartile range; IQR]. ACTH, Adrenocorticotropic hormone. AM, Morning. βCTX, Beta-C telopeptide cross-links of type I collagen. BF, Body fat. BM, Body mass. CCP, Combined contraceptive pill. CMJ, Countermovement jump. CRH, Corticotropin-releasing hormone. DBP, Diastolic blood pressure. F, Female. FM, Fat mass. HCC, Hair cortisol concentration. HDL, High-density lipoprotein. HPA, Hypothalamic–pituitary–adrenal. HPG, Hypothalamic–pituitary–gonadal. HR, Heart rate. IGF-1, Insulin-like growth factor 1. LDL, Low-density lipoprotein. LM, Lean mass. Ln, Natural logarithm. M, Male. MM, Muscle mass. NPY, Neuropeptide Y. NR, Not reported. PINP, Procollagen I N-terminal peptide. PM, Evening. POMS, Profile of mood states. RQ, Reporting quality. SBP, Systolic blood pressure. SERE, Survival, Evasion, Resistance, and Escape. Wk, Week. ‡ Data were extracted via WebPlotDigitizer v5 (https://automeris.io/) for the following studies: Conkright et al., 2021 [24], Gifford et al., 2019 [44], Gifford et al., 2025 [46], McFadden et al., 2024a [54], O’Leary et al., 2023 [59], O’Leary et al., 2024 [60], Strahler et al., 2015 [65]. # Identified via hand-searching (not with an electronic database search). † Study includes a recovery period.
Table 3.
Summary of the studies included in the scoping review that evaluated body composition.
| Author, Year |
Tactical Domain and Study Characteristics | Sample Characteristics | Body Composition Assessment and Outcomes | Other Markers Analyzed |
Impact of Stress and Sex on Body Composition | |
|---|---|---|---|---|---|---|
| Outcomes and Assessment Details | Aggregate-Level Study Data (Mean ± SD) a |
|||||
| Ahmed et al., 2020 [32] RQ: 53.1% |
Military Design: Prospective cohort (5 days); artic-like field training exercise at the Canadian Forces Base (Meaford, Ontario, Canada) Primary outcomes: Energy intake and expenditure |
|
Total: BMI (clothed), BM (clothed), FM, FFM, BF Methods: Deuterium isotope dilution (0.12 g 2H per est. kg TBW) Hydration status: NR Fasted status: NR |
BMI (F): Pre: 29.0 ± 4.5 kg/m2 Post: 28.3 ± 4.4 kg/m2 * Total BM (F): Pre: 81.8 ± 11.7 kg Post: 80.1 ± 11.0 kg * Total FM (F): Pre: 27.9 ± 6.4 kg Post: 24.9 ± 7.9 kg * Total FFM (F): Pre: 53.9 ± 5.2 kg Post: 55.3 ± 3.2 kg * Total BF (F): Pre: 31.4 ± 6.1% Post: 27.4 ± 8.2% * * p < 0.05 (time) |
Energetics: energy expenditure, energy intake, energy deficit, energy availability |
|
| Andrews et al., 2010 † [33] RQ: 51.6% |
Military Design: Cross-sectional; service members completing the Army Physical Fitness Test (Washington, DC, USA) Primary outcomes: Oxidative stress |
|
Total: BMI, BM, LM, FM, BF Regional: Trunk FM and trunk BF Methods: DXA (Hologic QDR Discovery Wi, Bedford, MA, USA) Hydration status: NR Fasted status: NR |
BMI (F): 29.9 ± 2.3 kg/m2 Total BM (F): 82.3 ± 11.0 kg * Total LM (F): 48.4 ± 5.9 kg * Total FM (F): 28.7 ± 4.0 kg Total BF (F): 36.0 ± 3.7% * Trunk FM (F): 13.1 ± 2.8 kg Trunk BF (F): 35.4 ± 5.2 kg * * p < 0.05 (sex) |
Baseline: Fitness level, dietary intake Oxidative stress: Creatine kinase, C-reactive protein, glutathione peroxidase, superoxide dismutase |
|
| Beckner et al., 2023 [34] RQ: 84.4% |
Military Design: Prospective cohort (17 days); Cadet Leader Development Training at the U.S. Military Academy (West Point, NY, USA) Primary outcomes: Body composition, performance, energy expenditure, endocrine and metabolic status, metabolomics |
|
Total: BM, dry LM, FM, TBW Methods: BIA (InBody 770, Cerritos, CA, USA) Hydration status: NR Fasted status: NR |
Total BM: Pre: 71.2 ± 10.6 kg * Post: 68.6 ± 10.7 kg ** Total dry LM: Pre: 14.2 ± 1.3 kg * Post: 14.2 ± 1.4 kg Total FM: Pre: 18.6 ± 7.6 kg * Post: 15.7 ± 7.3 kg Total TBW: Pre: 38.5 ± 3.3 kg Post: 38.7 ± 3.9 kg * p ≤ 0.05 (sex) ** p ≤ 0.05 (sex, post vs. pre change) |
Energetics: total daily energy expenditure (doubly labeled water) Endocrine status: estradiol, progesterone, total testosterone, free testosterone Metabolic status: serum glycerol, free fatty acids, serum leptin Metabolomics: all metabolites within the lipid super pathway Performance: lower body power |
|
| Charles et al., 2008 [35] RQ: 75.0% |
Police Design: Cross-sectional; Buffalo Cardio-metabolic Occupational Police Stress Study (Buffalo Police Department, Buffalo, NY, USA) Primary outcomes: Adiposity and oxidative stress |
|
Total: BMI, WC, waist-to-hip ratio, waist-to-height ratio, abdominal height Methods: Digital scale (clothed, without shoes), tape measure after exhale (nearest 0.5 cm) Hydration status: NR Fasted status: 12-h (for blood collection) |
BMI (F): 26.3 ± 4.6 kg/m2 * WC (F): 80.4 ± 10.2 cm * Waist-to-hip ratio (F): 0.77 ± 0.06 * Waist-to-height ratio (F): 0.48 ± 0.06 * Abdominal height (F): 19.0 ± 3.0 cm * * p < 0.001 (sex) |
Oxidative stress: Oxidative stress score, glutathione, glutathione peroxidase, vitamin C, thiobarbituric acid reactive substances, trolox equivalent antioxidant capacity |
|
| Cho et al., 2017 [36] RQ: 42.4% |
Military Design: Prospective cohort (8 wk); during 16-wk Officer training course at the Korea Third Military Academy (Yeongcheon, South Korea) Primary outcomes: Reproductive function |
|
Total: BM, BMI, WC Methods: Tape measurement during minimal respiration (WC) Hydration status: NR Fasted status: Overnight |
Total BM: 4 wk: 60.0 ± 6.8 kg 8 wk: 59.3 ± 6.4 kg * BMI: 4 wk: 22.7 ± 2.3 kg/m2 8 wk: 22.4 ± 2.2 kg/m2 * WC: 4 wk: 67.0 ± 5.8 cm 8 wk: 67.1 ± 4.6 cm * p < 0.05 (time) |
Reproductive function: regularity, CRH, cortisol, prolactin, endorphin-β, NPY, leptin, orexin-A, ghrelin, follicle-stimulating hormone, luteinizing hormone, estradiol, thyroid-stimulating hormone, thyroxine |
|
| Coge et al., 2024 ‡ [37] RQ: 65.6% |
Military Design: Prospective cohort (34 wk); recruit basic training (Instituto Superior Técnico Militar of Angola) Primary outcomes: Body composition, fitness, and performance |
|
Total: BM, BMI, FM Methods: BIA (OMRON HBF 510, Omron Healthcare, Inc., Hoffman Estates, IL, USA) Hydration status: NR Fasted status: NR |
Total BM (F): Pre: 65.5 ± 12.0 kg Post: 63.8 ± 11.4 kg *, ** BMI (F): Pre: 24.9 ± 5.3 kg/m2 Post: 24.2 ± 5.0 kg/m2 ** FM (F): Pre: 28.7 ± 4.6 kg Post: 27.2 ± 4.4 kg * p < 0.05 (sex), ** p < 0.01 (time) |
Fitness: VO2max, sprint performance Performance: CMJ, medicine ball throw, push-ups, curl-ups |
|
| Conkright et al., 2022 [38] RQ: 68.6% |
Military Design: Prospective cohort (5 days); simulated military operational stress protocol with restricted sleep and caloric intake Primary outcomes: Extracellular vesicle biomarkers |
|
Total: BM, BF Methods: Air displacement plethysmography (BOD POD, Cosmed, Concord, CA, USA) Hydration status: NR Fasted status: Overnight |
Total BM (F): 70.8 ± 8.1 kg * Total BF (F): 28.2 ± 6.7% * * p < 0.05 (sex) |
Performance: Baseline VO2peak, average knee extensor maximal voluntary contraction Extracellular vesicle biomarkers: Concentration, size Other: Contraceptive use, sleep, caloric intake, perceived exertion, myoglobin, creatine kinase |
|
| Cuddy et al., 2015 [39] RQ: 27.3% |
Fire Design: Prospective cohort (3 days); live wildland fire suppression (Fort Collins, CO, USA) Primary outcomes: Physiological strain, thermal responses, energy expenditure |
|
Total: BM Methods: Digital scale Hydration status: NR Fasted status: NR |
Total BM (F): Pre: 66.7 ± 4.4 Post: 65.7 ± 4.7 p-value NR |
Physiological strain: Physiological strain index rating, heart rate Thermal responses: Core and skin (chest) temperature Energetics: Energy expenditure, activity, water turnover |
|
| Dawes et al., 2023 [40] RQ: 64.5% |
Police Design: Retrospective cohort; archived health and fitness records from officers with ≥5 y experience Primary outcomes: Body composition and performance |
|
Total: BM, BMI Methods: Digital scale Hydration status: NR Fasted status: NR |
Total BM (F, n = 23): Year 1: 76.5 ± 14.9 kg Year 5: 79.1 ± 15.9 kg p = 0.106 (time) BMI (F, n = 24): Year 1: 26.2 ± 4.3 kg/m2 Year 5: 27.1 ± 4.4 kg/m2 p = 0.105 (time) |
Performance: Vertical jump height, sit-ups, push-ups Fitness: VO2max |
|
| Dicks et al., 2023 [41] RQ: 56.3% |
Police Design: Cross-sectional; physical readiness assessment (Midwestern Police Department) Primary outcomes: Physical Readiness Assessment performance and body composition |
|
Total: BM, BMI, BF, FFM Methods: BIA (Tanita, TBF-300A, Tokyo, Japan) Hydration status: NR Fasted status: NR |
Total BM (F): 73.3 ± 12.2 kg * BMI (F): 26.6 ± 2.5 kg/m2 Total BF (F): 33.7 ± 5.0% Total FFM (F): 48.2 ± 5.6 kg ** ** p < 0.001 (sex), * p < 0.05 (sex) |
Performance: Handgrip strength, physical activity rating, moderate-to-vigorous physical activity, time to complete the physical readiness assessment |
|
| Evans et al., 2008 [42] RQ: 60.6% |
Military Design: Prospective cohort (~4 months); Israeli Defense Force gender-integrated basic recruit training program (Tel Hashomer, Israel) Primary outcomes: Body composition, fitness, bone turnover, endocrine regulation, inflammation |
|
Total: LM, FM, BF Methods: four-site skinfolds (BF); weight multiplied by BF (FM); FM subtracted from weight (LM) Hydration status: NR Fasted status: Overnight |
Total LM (F): Pre: 41.9 ± 5.3 kg Post: 43.8 ± 5.0 kg * Total FM (F): Pre: 19.0 ± 5.8 kg Post: 18.3 ± 5.4 kg * Total BF (F): Pre: 30.7 ± 4.9% Post: 29.0 ± 4.5% * p < 0.002 (time) |
Fitness: VO2max, 2-km run time Bone turnover: Bone alkaline phosphatase, PINP, tartrate-resistant acid phosphatase, C-telopeptide cross-links of type I collagen Endocrine regulation: Albumin, calcium, PTH Inflammation: TNF-α, IL-1b, IL-6 |
|
| Gifford et al., 2021 [45] RQ: 81.8% |
Military Design: Prospective cohort (11 months); Commissioning Course (basic combat training) at the Royal Military Academy (Sandhurst, UK) Primary outcomes: Reproductive and metabolic function Part of the Female Endocrinology in Arduous Training (FEAT) Study |
|
Total: BM, FM, FFM, VAT Regional: FM and FFM for arms, legs, trunk, gynoid, android Methods: DXA (GE Lunar iDXA, GE Healthcare, Madison, WI, USA) Hydration status: NR Fasted status: 12-h |
Total BM: 14 wk: 63.3 ± 7.2 kg 29 wk: 64.7 ± 6.8 kg 43 wk: 64.3 ± 6.9 kg * Total FM: 14 wk: 14.5 ± 3.4 kg 29 wk: 16.2 ± 3.2 kg 43 wk: 15.6 ± 3.3 kg *** Total FFM: 14 wk: 49.1 ± 5.1 kg 29 wk: 48.5 ± 4.9 kg 43 wk: 48.7 ± 4.9 kg * VAT: 14 wk: 95.4 ± 72.5 g 29 wk: 132.5 ± 93.4 g 43 wk: 137.2 ± 72.6 g ** Regional FM—arms: 14 wk: 1.7 ± 0.4 kg 29 wk: 1.9 ± 0.4 kg 43 wk: 1.8 ± 0.4 kg ** Regional FM—legs: 14 wk: 6.2 ± 1.4 kg 29 wk: 6.7 ± 1.4 kg 43 wk: 6.5 ± 1.4 kg *** Regional FM—trunk: 14 wk: 5.8 ± 1.8 kg 29 wk: 6.8 ± 1.8 kg 43 wk: 6.4 ± 1.8 kg *** Regional FM—gynoid: 14 wk: 3.0 ± 0.7 kg 29 wk: 3.4 ± 0.7 kg 43 wk: 3.3 ± 0.7 kg *** Regional FM—android: 14 wk: 0.7 ± 0.3 kg 29 wk: 0.9 ± 0.3 kg 43 wk: 0.8 ± 0.3 kg *** Regional FFM—arms: 14 wk: 5.2 ± 0.7 kg 29 wk: 5.3 ± 0.7 kg 43 wk: 5.1 ± 0.7 kg * Regional FFM—legs: 14 wk: 16.8 ± 2.0 kg 29 wk: 61.6 ± 1.9 kg 43 wk: 16.6 ± 1.8 kg Regional FFM—trunk: 14 wk: 23.6 ± 2.5 kg 29 wk: 23.1 ± 2.4 kg 43 wk: 23.5 ± 2.6 kg *** p < 0.0001 (time) Regional FFM—gynoid: 14 wk: 7.7 ± 0.9 kg 29 wk: 7.5 ± 0.9 kg 43 wk: 7.6 ± 1.0 kg ** Regional FFM—android: 14 wk: 3.2 ± 0.4 kg 29 wk: 3.2 ± 0.4 kg 43 wk: 3.3 ± 0.4 kg * *** p < 0.0001, ** p ≤ 0.001, * p ≤ 0.02 (time) |
Fasting metabolic: Leptin, HOMA2 IR, IGF-1, glucose, nonesterified fatty acids, total triiodothyronine, free thyroxine, thyroid-stimulating hormone Basal reproductive: Luteinizing hormone, follicle-stimulating hormone (and its ratio), gonadotropin-releasing hormone, inhibin B, SHBG, free androgen index, DHEA, androstenedione, progesterone Others: C-peptide, creatinine, estradiol, anti-Müllerian hormone, prolactin, testosterone |
|
| Kargl et al., 2024 [49] RQ: 60.6% |
Military Design: Prospective cohort (10 wk); U.S. Marine Corps Officer Candidate School Primary outcomes: Inflammation, oxidative stress, stress, sleep, performance |
|
Total: BM, BMI Methods: Digital scale Hydration status: NR Fasted status: Not fasted |
Total BM (F): Wk 0: 66.3 ± 6.6 kg Wk 10: 66.2 ± 6.0 kg p > 0.05 (time) p < 0.05 (sex) BMI (F): Wk 0: 24.2 ± 1.7 kg/m2 Wk 10: 24.2 ± 1.9 kg/m2 p > 0.05 (time) p < 0.05 (sex) |
Inflammation: C-reactive protein, IL-6, IL-8, IL-10, TNF-α, interferon-γ Oxidative stress: Peroxidized lipid, protein carbonyls, and antioxidative capacity Sleep: Disturbances (Athlete Sleep Screening Questionnaire) Stress: Perceived Stress Scale Performance: Physical fitness and combat fitness test scores |
|
| Krugly et al., 2023 [50] RQ: 54.5% |
Police Design: Retrospective cohort; three semesters of police education in Sweden Primary outcomes: Fitness and mental health |
|
Total: BM, BMI Methods: Digital scale Hydration status: NR Fasted status: NR |
Total BM (F): Semester 1: 67.8 ± 7.9 kg Semester 3: 68.4 ± 7.9 kg BMI (F): Semester 1: 23.3 ± 2.4 kg/m2 Semester 3: 23.5 ± 2.3 kg/m2 p-values: NR |
Fitness: Push-ups, sit-ups, grip strength, VO2max, standing long jump, agility (Harres test and L-run test), self-reported physical activity Mental health: Self-reported mental health and perceived police ability |
|
| Lieberman et al., 2008 [51] RQ: 66.7% |
Military Design: Prospective cohort (13 wk); U.S. Marine Corps basic training (Parris Island, SC, USA) Primary outcomes: Body composition, metabolic status, mood state |
|
Total: BM, FM, FFM, BF, BMM Methods: DXA (DPX-L, Lunar Radiation Corp) Hydration status: NR Fasted status: Overnight |
Total BM: Wk 1: 63.9 ± 0.8 kg Wk 5: 61.8 ± 0.8 kg Wk 8: 61.4 ± 0.8 kg Wk 12: 61.7 ± 0.7 kg * Total FM: Wk 1: 19.5 ± 0.6 kg Wk 5: 16.2 ± 0.6 kg Wk 8: 15.2 ± 0.5 kg Wk 12: 14.7 ± 0.5 kg * Total FFM: Wk 1: 41.7 ± 0.5 kg Wk 5: 42.7 ± 0.5 kg Wk 8: 43.3 ± 0.5 kg Wk 12: 44.1 ± 0.5 kg * Total BF: Wk 1: 30.2 ± 0.7% Wk 5: 26.1 ± 0.7% Wk 8: 24.6 ± 0.7% Wk 12: 23.7 ± 0.7% * Total BMM: Wk 1: 2.8 ± 0.1 kg Wk 5: 2.8 ± 0.1 kg Wk 8: 2.8 ± 0.1 kg Wk 12: 2.9 ± 0.1 kg * p < 0.001 (time, vs. wk 1) |
Metabolic status: Cholesterol (total, LDL, HDL), free fatty acids, cortisol, glucose Mood state: POMS subscales (fatigue, confusion, depression, tension, anger, vigor) |
|
| Lieberman et al., 2012 [52] RQ: 60.6% |
Military Design: Prospective cohort (12 wk); U.S. Marine Corps basic training (Parris Island, SC, USA) Primary outcomes: Body composition, mood state, metabolic status |
|
Total: BM, FM, LM, BMM Methods: DXA (model DPX-L, LUNAR Radiation Corp, Madison, WI, USA) Hydration status: NR Fasted status: Overnight |
Total BM: Pre: 63.6 ± 5.5 kg Post: 62.1 ± 4.9 kg * Total FM: Pre: 19.0 ± 4.4 kg Post: 14.8 ± 3.4 * Total LM: Pre: 41.7 ± 3.7 kg Post: 44.4 ± 3.9 kg * Total BMM: Pre: 2.9 ± 0.4 kg Post: 3.0 ± 0.4 kg * p ≤ 0.001 (time) |
Mood state: POMS subscales (fatigue, confusion, depression, tension, anger, vigor) Metabolic status: Substance P, fructosamine, adrenocorticotropic hormone, cholesterol (total, HDL, LDL), triglycerides, free fatty acids, DHEA-S |
|
| McClung et al., 2009 [53] RQ: 60.6% |
Military Design: Prospective cohort (8 wk); U.S. Army basic combat training course (Fort Jackson, SC, USA) Primary outcomes: Iron status, performance, mood state |
|
Total: BM Methods: Digital scale Hydration status: NR Fasted status: Overnight |
Total BM—Iron: Pre: 61.8 ± 9.4 kg Post: 61.8 ± 8.2 kg Total BM—Placebo: Pre: 62.2 ± 8.5 kg Post: 61.9 ± 6.9 kg p-values: NR |
Iron status: Hemoglobin, red blood cell distribution width, ferritin, transferrin saturation, soluble transferrin receptor Performance: 2-mile run time Mood state: POMS subscales (fatigue, confusion, depression, tension, anger, vigor) |
|
| McFadden et al., 2024b [55] RQ: 72.7% |
Military Design: Prospective cohort (11 wk); U.S. Marine Corps basic training (Parris Island, SC, USA) Primary outcomes: Performance, resilience, wearable tracking Part of a larger study, the U.S. Marine Corps Gender-Integrated Recruit Training study |
|
Total: BM Methods: Digital scale Hydration status: NR Fasted status: NR |
Total BM (F): Wk 2: 62 ± 8 kg Wk 11: 61 ± 7 kg p-value NR |
Performance: Physical and combat fitness tests, lower body strength and power Resilience: Connor–Davidson Resilience Scale, workload, self-reported sleep, stress Wearable tracking: energy expenditure, distances, sleep, acceleration Other: Salivary cortisol |
|
| Nindl et al., 2012 [56] RQ: 57.6% |
Military Design: Prospective cohort (~4 months); Israeli Defense Force gender-integrated basic recruit training program (Tel Hashomer, Israel) Primary outcomes: Body composition, inflammation, fitness |
|
Total: BM, FM, FFM, BF Methods: Digital scale, four-site skinfolds (biceps, triceps, suprailiac, subscapular) Hydration status: NR Fasted status: Overnight (for blood collection) |
Total BM (F): Pre: 61.6 (1.1) kg Post: 62.7 (1.1) kg * Total FM (F): Pre: 19.6 (0.6) kg Post: 19.0 (0.6) kg *,** Total FFM (F): Pre: 42.0 (0.6) kg Post: 43.7 (0.5) kg *,** Total BF (F): Pre: 31.3 (0.5)% Post: 29.7 (0.5)% *,** * p < 0.05 (sex), ** p < 0.05 (time) |
Inflammation: IL-1β, IL-6, TNF-α, IGF-1, free IGF-1, IGF binding proteins-1, -2, -3, -4, -5, and -6 Fitness: VO2max |
|
| Øfsteng et al., 2020 † [57] RQ: 63.6% |
Military Design: Prospective cohort (17 days); 10-day military field exercise followed by 7 days of recovery Primary outcomes: Body composition and performance |
|
Total: BM, FM, FFM Methods: DXA (Lunar Prodigy densitometer, Prodigy Advance PA + 302 047, Lunar) Hydration status: NR Fasted status: Overnight |
Total BM (F): Data NR p = 0.02 (sex) p = 0.17 (sex × time) Total FM (F): Data NR p = 0.58 (sex) p = 0.64 (sex × time) Total FFM (F): Data NR p < 0.001 (sex) p = 0.15 (sex × time) |
Performance: Lower body strength and power, upper body strength, anaerobic power Energetics: Energy expenditure Sleep: Quantity Other: Testosterone, free testosterone, SHBG, IGF-1, cortisol, triiodothyronine, thyroxine, thyroid-stimulating hormone, creatine kinase, testosterone/cortisol ratio |
|
| O’Leary et al., 2023 † [59] RQ: 75.8% |
Military Design: Prospective cohort (36 h); field exercise in energy deficit as part of Commissioning Course at the Royal Military Academy (Sandhurst, UK) Primary outcomes: Bone turnover, diet, energy expenditure |
|
Total: BM Methods: Digital scale Hydration status: NR Fasted status: Overnight |
Total BM: Baseline: 61.6 ± 6.6 kg Exercise: 60.8 ± 7.2 kg Recovery: 61.5 ± 7.2 kg p > 0.05 (time) p < 0.05 (sex) |
Bone turnover: βCTX, PINP, PTH, total 25(OH)D, albumin-adjusted calcium, total 1,25(OH)2D, phosphate, total 24,25(OH)2D Diet: carbohydrate, protein, and fat intake Energetics: energy expenditure and balance (accelerometry and doubly labeled water) Other: Testosterone, cortisol |
|
| O’Leary et al., 2024 ‡ [60] RQ: 66.7% |
Military Design: Prospective cohort (44 wk); Commissioning Course (basic combat training program) at the Royal Military Academy (Sandhurst, UK) Primary outcomes: Energy balance, body composition, bone turnover, metabolic and endocrine statuses |
|
Total: LM, FM, BF Methods: DXA (Lunar iDXA, GE Healthcare, UK) Hydration status: NR Fasted status: ~10-h |
Total LM (F): Baseline: 47.4 ± 3.9 kg * Term 1: 47.0 ± 4.3 kg * Term 2: 46.7 ± 3.9 kg * Term 3: 46.5 ± 3.9 kg * Total FM (F): Baseline: 15.9 ± 4.0 kg Term 1: 14.6 ± 2.9 kg Term 2: 16.17 ± 2.7 kg ** Term 3: 16.6 ± 2.9 kg ** Total BF (F): Baseline: 24.7 ± 4.7% * Term 1: 23.5 ± 3.7% * Term 2: 25.6 ± 3.1% *,*** Term 3: 26.2 ± 2.7% *,*** * p < 0.05 (sex), ** p < 0.05 (time, vs. Term 1), *** p < 0.05 (time, vs. Baseline and Term 1) |
Energetics: energy intake, energy balance, energy expenditure, macronutrient intake Bone turnover: Bone alkaline phosphatase, βCTX, PINP Metabolic and endocrine statuses: Leptin, IGF-1, triiodothyronine, free thyroxine, TSH, testosterone, SHBG, free androgen index, cortisol |
|
| O’Leary et al., 2025 # [61] RQ: 75.8% |
Military Design: Prospective cohort (13 wk); basic combat training program (Army Training Centre, Pirbright, UK) Primary outcomes: Body composition, performance, iron status, vitamin D status, bone metabolism markers |
|
Total: FM, LM, full-body aBMD Regional: aBMD for trunk, arms, and legs Methods: DXA (Lunar iDXA; GE Healthcare, Buckinghamshire, UK) Hydration status: NR Fasted status: Overnight fast not possible for all participants |
Total FM, kg * Non-users Δ: −2.1 (−2.6, −1.5) Combined Δ: −2.2 (−3.0, −1.4) Progestin Δ: −2.0 (−2.6, −1.5) Total LM, kg * Non-users Δ: 2.1 (1.8, 2.5) Combined Δ: 2.1 (1.7, 2.6) Progestin Δ: 2.4 (2.1, 2.8) Full-body aBMD, mg/cm2 *,** Non-users Δ: 0.01 (0.01, 0.01) Combined Δ: 0.01 (−0.00, 0.02) Progestin Δ: 0.01 (−0.00, 0.01) Trunk aBMD, mg/cm2 ** Non-users Δ: 0.00 (−0.01, 0.00) Combined Δ: 0.00 (−0.01, 0.00) Progestin Δ: 0.00 (−0.01, 0.01) Arms aBMD, mg/cm2 * Non-users Δ: 0.01 (0.00, 0.02) Combined Δ: 0.01 (0.00, 0.03) Progestin Δ: 0.01 (0.00, 0.03) p < 0.001 (time) Δ Leg aBMD, mg/cm2 *,** Non-users Δ: 0.02 (0.01, 0.02) Combined Δ: 0.02 (0.01, 0.03) Progestin Δ: 0.01 (0.01, 0.02) * p < 0.001 (time), ** p ≤ 0.03 (group), group × time: all p > 0.05 |
Performance: 2.4-km run time, maximal lift strength, peak power output Iron status: Ferritin, hemoglobin Vitamin D status: Total 25(OH)D Bone metabolism markers: PTH, βCTX, PINP |
|
| Pasiakos et al., 2012 [62]; Margolis et al., 2012 [63] RQ: 63.6% |
Military Design: Prospective cohort (10 wk); basic combat training course (Fort Jackson, SC, USA) Primary outcomes: Body composition, cardiometabolic risk, diet, lifestyle factors |
|
Total: BM, BF, FFM, BF by BMI2 Methods: three-site skinfolds (chest, triceps, subscapular sites for men, triceps, suprailiac, abdominal sites for women) Hydration status: NR Fasted status: Overnight |
Total BM (F): Wk 0: 66.3 ± 8.3 kg Wk 3: 66.2 ± 7.8 kg Wk 6: 66.8 ± 7.6 kg * (vs. wk 3) Wk 9: 66.4 ± 7.4 kg Total BF (F): Wk 0: 26.6 ± 5.6% Wk 9: 22.8 ± 5.1% * Total FFM (F): Wk 0: 48.2 ± 4.8 kg Wk 9: 51.0 ± 5.3 kg * Total BF by BMI2 (F; <30 kg/m2): Wk 0: 26.3 ± 5.4 kg/m2 Wk 9: 22.9 ± 5.0 kg/m2 Total BF by BMI2 (F; ≥30 kg/m2): Wk 0: 35.9 ± 3.9 kg/m2 Wk 9: n = 0 * p < 0.05 (time) |
Cardiometabolic risk: Glucose, cholesterol (total, LDL, HDL), triglycerides Diet: Total fat, saturated fat, cholesterol, sodium, fiber, fruits, and vegetables Lifestyle factors: Family medical history (myocardial infarction, stroke, diabetes), smoking, sedentary behavior |
|
| Popp et al., 2024 [64] RQ: 78.8% |
Military Design: Prospective cohort (10 wk); basic combat training course (Fort Jackson, SC, USA) Primary outcomes: Body composition and reproductive function |
|
Total: BM, BMI, FFM, FM, BF Methods: DXA (Lunar Prodigy, GE Healthcare, Madison, WI, USA) Hydration status: NR Fasted status: Overnight |
Δ Total BM, kg: 1.1 (0.3, 1.9) * Δ BMI, kg/m2: 0.2 (−0.1, 0.6) Δ Total FFM, kg: 3.1 (2.7, 3.5) ** Δ Total FM, kg: −1.7 (−2.4, −1.0) ** Δ Total BF, %: −3.3 (−4.0, −2.6) ** p < 0.001, * p < 0.02 (time) |
Reproductive function: Leptin, free triiodothyronine, triiodothyronine, free thyroxine, thyroxine, IGF-1 Other: Cortisol |
|
| Szivak et al., 2018 †,# [22] RQ: 56.3% |
Military Design: Prospective cohort (2 wk); U.S. Navy SERE training (Kittery and Rangeley, ME, USA) Primary outcomes: Neuroendocrine markers and performance |
|
Total: BM Methods: Digital scale Hydration status: NR Fasted status: Yes (time-period not specified) |
Total BM (F): Baseline: 67.2 ± 5.1 kg Stress: 63.5 ± 5.2 kg Recovery: 63.3 ± 5.0 kg p-value NR |
Physical performance: Dominant handgrip strength, vertical jump height Neuroendocrine markers: Epinephrine, norepinephrine, dopamine, cortisol, testosterone, NPY |
|
| Szivak et al., 2023 [66] RQ: 62.5% |
Military Design: Cross-sectional; survey of U.S. Military Academy graduates between 1980 and 2011 (West Point, NY, USA) Primary outcomes: Obesity status, activity level, self-reported health status |
|
Total: BMI, BMI category Methods: Self-report from survey Hydration status: NR Fasted status: NR |
BMI (F): 25.9 ± 5.5 kg/m2 BMI Category (F): Underweight: 0.7% Normal: 53.1% Overweight: 29.6% Obese: 16.6% p-values (sex): NR |
Activity level: Self-reported; volume per week and activity level rating (low, moderate, high) vs. peers of the same age and sex Self-reported health status: Cardiovascular risk factors, eating behaviors, concerns about appearance, weight, and health |
|
| Vikmoen et al., 2020 † [68] RQ: 66.7% |
Military Design: Prospective cohort (14 days) during a 6-day field-based Selection Exercise at Rena Military Camp (Rena, Norway) Primary outcomes: Body composition and performance |
|
Total: BM, MM, FM Methods: BIA (InBody 720, Biospace Co., Fresno, CA, USA) Hydration status: NR Fasted status: Overnight |
Total BM (F): Pre: 67.7 ± 5.5 kg Post 0 h: 65.1 ± 5.4 kg * Post 24 h: 65.8 ± 5.5 kg * Post 72 h: 67.4 ± 6.3 kg Post 1 wk: 68.0 ± 5.7 kg Post 2 wk: 68.1 ± 5.7 kg Total MM (F): Pre: 32.0 ± 1.9 kg Post 0 h: 31.9 ± 2.3 kg Post 24 h: 31.9 ± 2.3 kg Post 72 h: 32.6 ± 2.4 kg Post 1 wk: 32.6 ± 2.1 kg * Post 2 wk: 31.5 ± 2.0 kg Total FM (F): Pre: 10.8 ± 3.7 kg Post 0 h: 8.0 ± 3.3 kg * Post 24 h: 8.5 ± 3.1 kg * Post 72 h: 9.1 ± 3.1 kg * Post 1 wk: 10.2 ± 3.2 kg Post 2 wk: 12.0 ± 3.4 kg * * p < 0.05 (time, vs. pre) |
Performance: CMJ height and maximal power, medicine ball throw, anaerobic performance Other: IGF-1, cortisol, testosterone, creatine kinase |
|
| Zurek et al., 2022 [69] RQ: 51.5% |
Military Design: Prospective cohort (7 months); command training at the Military University of Land Forces (Wroclaw, Poland) Primary outcomes: Body composition and performance |
|
Total: BM, BMI, BF, MM Methods: BIA (TANITA, model NR) Hydration status: NR Fasted status: NR |
Total BM (F): Phase 1: 63.1 ± 3.8 kg * Phase 2: 62.0 ± 3.5 kg * BMI (F): Phase 1: 22.4 ± 1.2 kg/m2 * Phase 2: 22.1 ± 1.3 kg/m2 * Total BF (F): Phase 1: 22.4 ± 3.2% * Phase 2: 22.0 ± 3.1% * Total MM (F): Phase 1: 45.0 ± 2.3 kg * Phase 2: 44.9 ± 1.9 kg * * p ≤ 0.0006 (sex) |
Performance: Handgrip strength, horizontal jump distance, sit-ups, shuttle run, 1000-m run, executive function, shooting performance |
|
a Summarized as mean ± standard deviation (SD), mean (standard error) or Δ (95% confidence interval; CI). aBMD, Areal bone mineral density. βCTX, Beta-C telopeptide cross-links of type I collagen. BIA, Bioelectric impedance analysis. BF, Body fat. BM, Body mass. BMI, Body mass index. BMM, Bone mineral mass. CMJ, Countermovement jump. CRH, Corticotropin-releasing hormone. DHEA, Dihydroepiandrostenedione. DHEA-S, Dehydroepiandrosterone sulfate. DXA, Dual energy X-ray absorptiometry. F, Female. FFM, Fat-free mass. FM, Fat mass. HDL, High-density lipoprotein. HOMA2 IR, Homeostatic modeling assessment of insulin resistance 2. HPA, Hypothalamic–pituitary–adrenal. HPG, Hypothalamic–pituitary–gonadal. HPO, Hypothalamic–pituitary–ovarian. IL, Interleukin. IGF, Insulin-like growth factor. LM, Lean mass. LDL, Low-density lipoprotein. M, Male. MM, Muscle mass. NPY, Neuropeptide Y. PINP, Procollagen I N-terminal peptide. POM, Profile of mood states. PTH, Parathyroid hormone. RQ, Reporting quality. SERE, Survival, Evasion, Resistance, and Escape. SHBG, Sex hormone-binding globulin. TBW, Total body water. TNF-α, Tumor necrosis factor α. VAT, Visceral adipose tissue. VO2max, maximal oxygen uptake. WC, Waist circumference. ‡ Data were extracted via WebPlotDigitizer v5 (https://automeris.io/) for the following studies: Coge et al., 2024 [37], O’Leary et al., 2024 [60]. # Identified via hand-searching (not with an electronic database search). † Study includes a recovery period.
Table 4.
Summary of the studies included in the scoping review that evaluated occupational performance.
| Author, Year |
Tactical Domain and Study Characteristics | Occupational Performance Assessment and Outcomes | Other Markers Analyzed |
Impact of Stress and Sex on Performance |
||
|---|---|---|---|---|---|---|
| Sample Characteristics | Outcomes and Assessment Details | Aggregate-Level Study Data (Mean ± SD) a |
||||
| Andrews et al., 2010 † [33] RQ: 51.6% |
Military Design: Cross-sectional; service members completing the Army Physical Fitness Test (Washington, DC, USA) Primary outcomes: Oxidative stress |
|
|
Estimated VO2max (F): 32.5 ± 5.1 mL/kg/min p > 0.05 (sex) |
Baseline: Body composition, dietary intake Oxidative stress: Creatine kinase, C-reactive protein, glutathione peroxidase, superoxide dismutase |
|
| Beckner et al., 2023 [34] RQ: 81.3% |
Military Design: Prospective cohort (17 days); Cadet Leader Development Training at the U.S. Military Academy (West Point, NY, USA) Primary outcomes: Body composition, performance, energy expenditure, endocrine and metabolic status, metabolomics |
|
|
Peak power (F): Pre: 3780 [IQR: 499] W Post: 3634 [IQR: 776] W p-value NR (time) p = 0.085 (sex) Average power (F): Pre: 3788 [IQR: 588] W Post: 3659 [IQR: 8680] W p-value NR (time) p = 0.079 (sex) |
Body composition: BM, dry LM, FM, TBW Energetics: total daily energy expenditure (doubly-labeled water) Endocrine status: estradiol, progesterone, total testosterone, free testosterone Metabolic status: serum glycerol, free fatty acids, serum leptin Metabolomics: all metabolites within the lipid superpathway |
|
| Coge et al., 2024 ‡ [37] RQ: 65.6% |
Military Design: Prospective cohort (34 wk); recruit basic training (Instituto Superior Técnico Militar of Angola) Primary outcomes: Body composition, fitness, and performance |
|
|
VO2max (F): Pre: 33.2 ± 6.5 mL/kg/min Post: 34.1 ± 6.3 mL/kg/min * Sprint performance (F): Pre: 5.4 ± 0.8 m/s Post: 5.8 ± 0.7 m/s * CMJ height (F): Pre: 24.8 ± 7.4 cm Post: 28.5 ± 7.8 cm * Medicine ball throw (F): Pre: 3.9 ± 0.9 m Post: 4.7 ± 0.9 m * Push-ups completed (F): Pre: 21.0 ± 5.6 Post: 23.5 ± 5.1 * Curl-ups completed (F): Pre: 63.6 ± 20.8 Post: 67.7 ± 20.2 * * p < 0.01 (time) |
Body composition: BM, BMI, FM |
|
| Conkright et al., 2021 [24] RQ: 57.6% |
Military Design: Prospective cohort; 5-day simulated military operational stress protocol (Pittsburgh, PA, USA) Primary outcomes: Neuromuscular performance, mood state, and hormonal responses |
|
|
Jump height (F) *** Day 1, Pre: 21.0 ± 4.6 cm Mid: 19.2 ± 4.6 cm ** Post: 18.2 ± 5.2 cm ** Day 2, Pre: 19.4 ± 4.4 cm Mid: 19.0 ± 4.5 cm ** Post: 19.1 ± 4.4 cm ** Day 3, Pre: 19.6 ± 4.5 cm Mid: 18.6 ± 5.1 cm ** Post: 17.9 ± 5.5 cm ** Day 4, Pre: 19.3 ± 4.2 cm Mid: 18.9 ± 5.5 cm ** Post: 18.3 ± 5.1 cm ** Maximum force prior to takeoff (F) *** Day 1, Pre: 1519 ± 240 N Mid: 1642 ± 228 N Post: 1661 ± 197 N Day 2, Pre: 1523 ± 204 N Mid: 1678 ± 255 N Post: 1713 ± 237 N Day 3, Pre: 1572 ± 247 N Mid: 1694 ± 240 N Post: 1642 ± 340 N Day 4, Pre: 1609 ± 254 N Mid: 1691 ± 228 N Post: 1642 ± 340 N ** Water can carry (F) *** Day 1: 0.98 ± 0.35 m/s Day 2: 1.07 ± 0.42 m/s Day 3: 0.96 ± 0.31 m/s Day 4: 1.00 ± 0.37 m/s Fire and movement (F) Day 1: 152.2 ± 13.3 s * Day 2: 157.4 ± 19.2 s * Day 3: 150.7 ± 17.0 s * Day 4: 145.7 ± 15.2 s * Casualty drag (F) *** Day 1: 82.0 ± 32.2 s Day 2: 72.7 ± 23.1 s Day 3: 67.5 ± 11.0 s Day 4: 67.1 ± 15.3 s 300-m shuttle (F) *** Day 1: 109.1 ± 14.8 s Day 2: 109.8 ± 15.7 s Day 3: 113.3 ± 16.7 s * Day 4: 113.5 ± 17.9 s * 300-m shuttle (loaded) (F) Day 1: 128.9 ± 19.8 s Day 2: 128.9 ± 21.4 s Day 3: 133.5 ± 23.7 s Day 4: 130.3 ± 18.8 s 4-mile ruck march (F) Day 1: 1659.9 ± 149.8 s Day 2: 1599.4 ± 138.6 s Day 3: 1645.8 ± 252.5 s Day 4: 1604.7 ± 146.5 s * p ≤ 0.001 (day, vs. day 1), ** p ≤ 0.001 (time, vs. pre), *** p ≤ 0.02 (main effect, sex) |
Hormonal responses: Growth hormone, IGF-1, brain-derived neurotrophic factor., cortisol Mood state: POMS subscales (tension, depression, anger, fatigue, confusion, vigor) |
|
| Conkright et al., 2022 [38] RQ: 68.8% |
Military Design: Prospective cohort (5 days); simulated military operational stress protocol with restricted sleep and caloric intake Primary outcomes: Extracellular vesicle biomarkers |
|
|
VO2peak (F): 39.0 ± 5.2 mL/kg/min * MVC—knee extensor (F): 900.1 ± 234.5 N * p < 0.05 (sex) |
Body composition: BM, BF Extracellular vesicle biomarkers: Concentration, size Other: Contraceptive use, sleep, caloric intake, perceived exertion, myoglobin, creatine kinase |
|
| Dawes et al., 2023 [40] RQ: 64.5% |
Police Design: Retrospective cohort; archived health and fitness records from officers with ≥5 y experience Primary outcomes: Body composition and performance |
|
|
Vertical jump height (F, n = 21): Year 1: 35.0 ± 8.0 cm Year 5: 34.4 ± 5.4 cm Sit-ups completed (F, n = 28): Year 1: 31.4 ± 8.0 Year 5: 35.0 ± 10.8 * Push-ups completed (F, n = 23): Year 1: 23.0 ± 11.8 Year 5: 25.9 ± 14.0 VO2max (F, n = 29): Year 1: 27.2 ± 5.2 mL/kg/min Year 5: 29.0 ± 5.4 mL/kg/min * p ≤ 0.001 (time) |
Body composition: BM, BMI |
|
| Dicks et al., 2023 [41] RQ: 56.3% |
Police; physical readiness assessment Design: Cross-sectional; physical readiness assessment (Midwestern Police Department) Primary outcomes: Physical Readiness Assessment performance and body composition |
|
|
Handgrip strength (F): 41.0 ± 9.6 kg ** Moderate-to-vigorous PA (F): 30.9 ± 11.5 min/day PA rating (F): 6.2 ± 0.5 * Physical readiness assessment time (F): 304.4 ± 45.0 s Estimated VO2max (F): 37.9 ± 2.2 mL/kg/min * p < 0.05 (sex), ** p < 0.001 (sex) |
Body composition: BM, BMI, BF, FFM |
|
| Evans et al., 2008 [42] RQ: 60.6% |
Military Design: Prospective cohort (~4 months); Israeli Defense Force gender-integrated basic recruit training program (Tel Hashomer, Israel) Primary outcomes: Body composition, fitness, bone turnover, endocrine regulation, inflammation |
|
|
VO2max (F): Pre: 36.7 ± 6.2 mL/kg/min Post: 39.7 ± 5.8 mL/kg/min p < 0.002 (time) 2-km run time (F): Pre: 742.5 ± 117.6 s Post: 688.3 ± 90.4 s p < 0.002 (time) |
Body composition: LM, FM, BF Bone turnover: Bone alkaline phosphatase, PINP, tartrate-resistant acid phosphatase, C-telopeptide cross-links of type I collagen Endocrine regulation: Albumin, calcium, PTH Inflammation: TNF-α, IL-1b, IL-6 |
|
| Greer et al., 2023 [47] RQ: 77.4% |
Military Design: Cross-sectional; women seeking care in urogynecology, family medicine, and women’s health clinics between December 2019 and February 2020 Primary outcomes: Psychological stress, impacts of pelvic floor disorders on Naval duties |
|
|
Physical fitness test failure rate by group: No pelvic floor disorder (n = 55): 14.6% ≥1 pelvic floor disorder (n = 123): 26.0% p = 0.064 (group) |
Psychological stress: Perceived Stress Scale score Impact of pelvic floor disorders on Naval duties: Body composition assessment failure, days missed work, deployment, limited duty profile |
|
| Kargl et al., 2024 [49] RQ: 60.6% |
Military Design: Prospective cohort (10 wk); USMC Officer Candidate School Primary outcomes: Inflammation, oxidative stress, stress, sleep, performance |
|
|
Physical fitness test (F): Wk 0: 273.6 ± 14.6 Wk 7: 267.9 ± 19.9 p < 0.05 (time) Combat fitness test (F): Wk 4: 281.4 ± 16.7 p > 0.05 (sex) |
Inflammation: C-reactive protein, IL-6, IL-8, IL-10, TNF-α, IFN-γ Oxidative stress: Peroxidized lipid, protein carbonyls, and antioxidative capacity Sleep: Disturbance (Athlete Sleep Screening Questionnaire) Stress: Perceived stress (Perceived Stress Scale) |
|
| Krugly et al., 2023 [50] RQ: 54.5% |
Police; police education program Design: Retrospective cohort; three semesters of police education in Sweden Primary outcomes: Fitness and mental health |
|
|
Push-ups completed (F): Semester 1: 24.7 ± 11.7 Semester 3: 29.7 ± 12.5 ** Sit-ups completed (F): Semester 1: 49.5 ± 12.5 Semester 3: 53.6 ± 11.9 ** Grip strength, N—right (F): Semester 1: 377.1 ± 66.6 Semester 3: 3921.0 ± 63.9 ** Grip strength, N—left (F): Semester 1: 353.3 ± 60.3 Semester 3: 369.3 ± 60.6 ** VO2max, mL/kg/min (F): Semester 1: 40.4 ± 5.3 Semester 3: 40.9 ± 4.9 * Standing long jump, cm (F): Semester 1: 183.1 ± 22.8 Semester 3: 186.2 ± 221.0 ** L-run test, s (F): Semester 1: 6.7 ± 1.2 Semester 3: 6.5 ± 0.3 * Harres test, s (F): Semester 1: 13.9 ± 1.3 Semester 3: 14.0 ± 1.8 * p ≤ 0.03 (time), ** p < 0.001 (time) |
Mental health: Self-reported mental health and perceived police ability |
|
| McClung et al., 2009 ‡ [53] RQ: 57.6% |
Military Design: Prospective cohort (8 wk); U.S. Army basic combat training course (Fort Jackson, SC, USA) Primary outcomes: Iron status, performance, mood state |
|
|
2-mile run time: Placebo (normal): 1057.8 ± 71.6 s Iron (normal): 1086.1 ± 86.7 s Placebo (iron-deficient): 1101.7 ± 102.7 s Iron (iron-deficient): 1053.3 ± 73.4 s * Placebo (anemia): 1192.2 ± 95.6 s ** Iron (anemia): 1082.2 ± 125.0 s * p < 0.05 (within-group, iron-normal vs. iron-deficient) ** p < 0.001 (between-group, placebo vs. iron-treated) |
Iron status: Hemoglobin, red blood cell distribution width, ferritin, transferrin saturation, soluble transferrin receptor Mood state: POMS subscales (fatigue, confusion, depression, tension, anger, vigor) |
|
| McFadden et al., 2024a [54] RQ: 72.7% |
Military Design: Prospective cohort (13 wk); USMC basic training (Parris Island, SC, USA) Primary outcomes: Sex differences in workload, sleep, stress, and performance Part of a larger study, the USMC Gender-Integrated Recruit Training study |
|
|
CMJ (F): Wk 2: 2329 ± 372 W Wk 11: 2201 ± 342 W * CMJREL (F): Wk 2: 37.6 ± 4.9 W/kg Wk 11: 35.7 ± 4.2 W/kg * IMTP (F): Wk 2: 1734 ± 363 N Wk 11: 1736 ± 357 N IMTPREL (F): Wk 2: 27.5 ± 4.6 N/kg Wk 11: 28.0 ± 4.8 N/kg * * p < 0.05 (time) |
Workload: Energy expenditure (relative to BM), distance, steps Stress: Salivary cortisol Sleep: Continuity and duration |
|
| McFadden et al., 2024b [55] RQ: 72.7% |
Military Design: Prospective cohort (11 wk); USMC basic training (Parris Island, SC, USA) Primary outcomes: Performance, resilience, wearable tracking Part of a larger study, the USMC Gender-Integrated Recruit Training study |
|
|
Physical fitness score (F): Wk 5: 231 ± 37 Wk 8: 250 ± 31 Combat fitness score (F): Wk 4: 238 ± 34 Wk 7: 264 ± 24 CMJ (F): Wk 2: 2358 ± 370 W Wk 11: 2201 ± 342 W IMTP (F): Wk 2: 1747 ± 373 N Wk 11: 1736 ± 357 N p-values: NR for outcomes of interest |
Resilience: Connor–Davidson Resilience Scale, workload, self-reported sleep, stress Wearable tracking: energy expenditure, distances, sleep, acceleration Other: Salivary cortisol |
|
| Nindl et al., 2012 [56] RQ: 57.6% |
Military Design: Prospective cohort (~4 months); Israeli Defense Force gender-integrated basic recruit training program (Tel Hashomer, Israel) Primary outcomes: Body composition, inflammation, fitness |
|
|
VO2max (F): Pre: 36.9 (0.7) mL/kg/min Post: 39.5 (0.6) mL/kg/min p < 0.05 (sex) p < 0.05 (time) |
Body composition: BM, FM, FFM, BF Inflammation: IL-1β, IL-6, TNF-α, IGF-1, free IGF-1, IGFBP-1, IGFBP-2, IGFBP-3, IGFBP-4, IGFBP-5, IGFBP-6 |
|
| Øfsteng et al., 2020 † [57] RQ: 63.6% |
Military Design: Prospective cohort (17 days); 10-day military field exercise followed by 7 days of recovery Primary outcomes: Body composition and performance |
|
|
One-RM leg press (F) p < 0.05 (sex) CMJ power (F) p < 0.05 (sex) p ≤ 0.02 (sex × time) One-RM bench press (F) p < 0.05 (sex) p ≤ 0.001 (sex × time) Wingate—peak power (F) p < 0.05 (sex) p ≤ 0.001 (sex × time) Wingate—mean power (F) p < 0.05 (sex) p ≤ 0.001 (sex × time) Data NR for women; significance levels reported |
Body composition: BM, FM, FFM Energetics: Energy expenditure Sleep: Quantity Other: Testosterone, free testosterone, SHBG, IGF-1, cortisol, T3, T4, TSH, creatine kinase, testosterone/cortisol ratio |
|
| O’Leary et al., 2018 ‡ [58] RQ: 72.7% |
Military Design: Prospective cohort (1 day); 9.7-km loaded march (~90-min, 11 or 16 kg backpack and 4 kg rifle) as part of 14-wk British Army SE Phase One training (Army Training Centre, Pirbright, UK) Primary outcomes: Neuromuscular function and physiological strain |
|
|
MVC (F): Pre: 400 (17) N Post: 365 (13) N p < 0.05 (time) Vertical jump height (F): Pre: 33.9 (1.0) cm Post: 32.2 (1.2) cm p < 0.05 (time) |
Physiological strain: heart rate, rating of perceived exertion |
|
| O’Leary et al., 2025 # [61] RQ: 75.8% |
Military Design: Prospective cohort (13 wk); basic combat training program (Army Training Centre, Pirbright, UK) Primary outcomes: Body composition, performance, iron status, vitamin D status, bone metabolism markers |
|
|
2.4-km run time (Δ, Wk 13 vs. Wk 1) * Non-users: −25 s (−33, −17) Combined: −30 s (−42, −19) Progestin-only: −27 s (−39, −15) Maximal strength (Δ, Wk 13 vs. Wk 1) * Non-users: 1.5 kg (−0.2, 3.1) Combined: 1.2 kg (−0.8, 3.1) ** Progestin: 1.9 kg (−0.5, 4.2) CMJ peak power (Δ, Wk 13 vs. Wk 1) * Non-users: 55 W (−5, 114) Combined: 27 W (−65, 119) Progestin-only: 2 W (−74, 77) * p ≤ 0.02 (main effect, time), ** p ≤ 0.05 (group, vs. non-users) |
Body composition: FM, LM, areal bone mineral density (whole-body and regional: trunk, arms, and legs) Iron status: Ferritin, hemoglobin Vitamin D status: Total 25(OH)D Bone metabolism markers: PTH, βCTX, PINP |
|
| Szivak et al., 2018 †,# [22] RQ: 62.5% |
Military Design: Prospective cohort (2 wk); U.S. Navy SERE training (Kittery and Rangeley, ME, USA) Primary outcomes: Neuroendocrine markers and performance |
|
|
Handgrip strength: Baseline: 33.5 ± 3.2 kg Stress: 30.0 ± 5.0 kg Vertical jump height: Baseline: 39.4 ± 6.8 cm Stress: 35.9 ± 7.4 cm p-values: NR for outcomes of interest |
Neuroendocrine markers: Epinephrine, norepinephrine, dopamine, cortisol, testosterone, NPY |
|
| Vikmoen et al., 2020 † [68] RQ: 66.7% |
Military Design: Prospective cohort (14 days) during a 6-day field-based Selection Exercise at Rena Military Camp (Rena, Norway) Primary outcomes: Body composition and performance |
|
|
CMJ height (F): Pre: 29.0 ± 3.6 cm Post 0 h: 23.5 ± 3.8 cm * Post 24 h: 24.2 ± 3.8 cm * Post 72 h: 24.8 ± 3.4 cm * Post 1 wk: 24.1 ± 3.7 cm * Post 2 wk: 26.3 ± 3.1 cm * CMJ maximal power (F): Pre: 2650 ± 384 W Post 0 h: 2265 ± 280 W * Post 24 h: 2387 ± 357 W * Post 72 h: 2394 ± 309 W * Post 1 wk: 2388 ± 333 W * Post 2 wk: 2540 ± 310 W Evacuation test (F): Pre: 45.6 ± 2.5 s Post 0 h: 67.0 ± 15.0 s * Post 24 h: 57.4 ± 4.9 s * Post 72 h: 51.9 ± 4.9 s * Post 1 wk: 49.7 ± 3.6 s * Post 2 wk: 47.2 ± 2.4 s * Medicine ball throw (F): Pre: 3.7 ± 0.3 m Post 0 h: 3.2 ± 0.3 m * Post 24 h: 3.4 ± 0.3 m Post 72 h: 3.5 ± 0.3 m Post 1 wk: 3.5 ± 0.3 m Post 2 wk: 3.6 ± 0.3 m * p < 0.05 (time, vs. Pre) |
Body composition: BM, MM, FM Other: IGF-1, cortisol, testosterone, creatine kinase |
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| Zurek et al., 2022 [69] RQ: 51.5% |
Military Design: Prospective cohort (7 months); command training at the Military University of Land Forces (Wroclaw, Poland) Primary outcomes: Body composition and performance |
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Handgrip strength (F): Phase 1: 87.5 ± 14.2 kg ** Phase 2: 93.3 ± 10.7 kg ** Sit-ups completed (F): Phase 1: 28.1 ± 3.1 ** Phase 2: 27.9 ± 3.7 * Horizontal jump distance (F): Phase 1: 187.0 ± 17.0 cm ** Phase 2: 186.8 ± 19.9 cm ** Shuttle run time (F): Phase 1: 19.8 ± 0.8 s ** Phase 2: 19.2 ± 1.4 s ** 1000-m run time (F): Phase 1: 245.4 ± 14.3 s ** Phase 2: 239.9 ± 22.7 s ** Color Trails Test-2 (F): Phase 1: 60.2 ± 12.0 s Phase 2: 58.7 ± 11.4 s Shooting performance (F): Phase 1: 3.1 ± 1.0 Phase 2: 4.4 ± 0.4 * p ≤ 0.02 (sex), ** p ≤ 0.0001 (sex) |
Body composition: BM, BMI, BF, MM |
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a Summarized as mean ± standard deviation (SD), mean (standard error), Δ (95% confidence interval; CI) or median [interquartile range; IQR]. BF, Body fat. BM, Body mass. BMI, Body mass index. CMJ, Countermovement vertical jump. CMJREL, CMJ relative to body mass. FFM, Fat-free mass. FM, Fat mass. F, Female. IGF-1, Insulin-like growth factor 1. IMTP, Isometric mid-thigh pull. IMTPREL, IMTP relative to body mass. LM, Lean mass. M, Male. MFPTT, Maximum force prior to takeoff. MM, Muscle mass. MVC, Maximal voluntary contraction. N, Newtons. NR, Not reported. PA, Physical activity. PINP, Procollagen I N-terminal peptide. RM, Repetition maximum. RQ, Reporting quality. SERE, Survival, Evasion, Resistance, and Escape. USMC, U.S. Marine Corps. W, Watts. VO2max, maximal oxygen uptake. VO2peak, peak oxygen uptake. ‡ Data were extracted via WebPlotDigitizer v5 (https://automeris.io/) for the following studies: Coge et al., 2024 [37], McClung et al., 2009 [53], O’Leary et al., 2018 [58]. # Identified via hand-searching (not with an electronic database search). † Denotes a study that includes a recovery period.
3.1. Critical Appraisal of Individual Sources of Evidence
In the total sample, included studies achieved “moderate” reporting quality (~63%) despite widely varying scores (27–88%). Four studies achieved “low” reporting quality (<50% of checklist items were completely reported; mean score = 44.3%) [36,39,43,67], and only three studies achieved “high” reporting quality (≥80% of checklist items were completely reported; mean score = 83.3%) [34,45,59].
Studies were most likely to completely report (≥80%) on items relating to adequately describing the study and key findings in the abstract (item 1b), the background and rationale (item 2), the variables to be measured (including the measures and tools) and how they will be handled in analyses (items 7, 8 and 11), reporting the characteristics of their sample and outcomes of interest (items 14a, 15, and 16a), and finally, summarizing and interpreting their findings in the discussion section (items 18 and 20).
Studies were least likely to completely report on items relating to how their sample size was determined (item 10), considering and describing any sensitivity analyses (item 12e), and the use of a flow diagram to document participant flow and missing data (item 13c). A summary of these individual reporting items (expressed as a percentage of checklist items that were completely reported) is provided in Table S3 as part of the Supplementary Materials.
3.2. Adrenal Stress and Neuroendocrine Responses
Nineteen studies (970 women; [Mean ± SD] age = 27 ± 8 y; body mass index [BMI] = 25.3 ± 3.0 kg/m2; BF = 29.9% ± 4.9%) evaluated sympathoadrenal responses to occupational stress in tactical populations, the majority of which were conducted in military settings (84%; 16 studies). Only three studies focused on non-military personnel: two in police officers (105 women) [65,67] and one in EMS (28 women) [48]. Most military studies assessed women undergoing basic training or officer candidate school (63%), with only a few involving active-duty personnel (e.g., McGraw et al., 2013 [31]; Andrews et al., 2010 [33]). More than half of the included studies involved mixed samples of women and men, with only 37% (7 studies) focusing exclusively on women. See Table 2 for the individual summaries of the coded dimensions for each study.
One-fourth (26%) of the included studies used a cross-sectional design [33,43,48,65,67], and only one study [31] used an acute pre–post intervention design; the remaining studies were prospective cohort studies. Studies that examined adrenal stress and neuroendocrine responses achieved “moderate” reporting quality (63.1% ± 13.1%) despite widely varying scores (347–88%), and only one study completely reported on ≥80% of checklist items (89.4%) [59].
Cortisol was the most assessed biomarker of adrenal stress, measured either via saliva, blood plasma, or hair. Six studies evaluated salivary cortisol, ten included plasma or serum cortisol, and three incorporated hair cortisol analysis. Notably, catecholamines (e.g., epinephrine, norepinephrine), which are direct indicators of sympathetic nervous system (SNS) activity, were absent from all included studies. Only one study (Gifford et al., 2019 [44]) included an adrenal function test as a proxy for overall HPA axis reactivity. Additional hormonal markers were assessed in several studies to provide insight into stress adaptation, including testosterone (Tomei et al., 2008 [67]), insulin-like growth factor (IGF-I) and inflammatory cytokines (Nindl et al., 2012 [56]), and lastly, estradiol, prolactin, and neuropeptide Y (Cho et al., 2017 [36]). However, sex hormones were infrequently evaluated despite their relevance to stress and reproductive health in women. Sympathoadrenal activity was measured during diverse occupational conditions, including military field training, selection courses, urban policing environments, and simulated combat. Elevated cortisol concentrations were generally observed in response to physical and psychological stress, and findings varied by training phase, environmental conditions, and participant experience level. However, despite this trend in heightened cortisol response to various stressors, we note that two studies observed declining cortisol over time (Lieberman et al., 2012 [52]; Strahler et al., 2015 [65]), which would suggest possible stress adaptations.
3.3. Body Composition
Twenty-nine studies (2912 women; age = 25.2 ± 6.6 y; BMI = 25.2 ± 2.2 kg/m2; BF = 28.3% ± 5.3%) were identified that either focused on or included anthropometrics and/or body composition as part of their primary outcomes. Notably, most studies included mixed samples, and only 11 (38%) focused exclusively on women. Studies were overwhelmingly conducted in military populations (82%) including those representative of the U.S., e.g., Army (West Point or Basic Combat Training) [33,34,52,53,62,64,66], Navy [22], Marine Corps [49,51], with only five studies (17%) focusing on law enforcement [35,40,41,50] and fire service [39]. Further, over three-fourths of included studies (79%) assessed women undergoing basic training or officer candidate school, with only a few involving active-duty personnel [22,33,35,38,40,41,47,57,66]. See Table 3 for the individual summaries of the coded dimensions for each study.
Four studies used a cross-sectional study design [33,35,41,66], with another two using a retrospective study design [40,50]; the remaining studies utilized a prospective cohort design. Studies that examined body composition outcomes achieved “moderate” reporting quality (63.0% ± 11.9%) despite widely varying scores (27–84%), and only two studies completely reported on ≥80% of checklist items (81.8%) [45,64].
Ten studies reported only anthropometric data [35,36,39,40,49,50,53,54,59], eighteen studies reported body composition outcomes [22,32,33,34,37,38,41,42,45,51,52,56,57,60,61,62,64,68,69], and one study focused on self-reported anthropometric data to calculate BMI [66]. Of the body composition assessment approaches, the methods employed (presented from most used to least) included dual energy X-ray absorptiometry [33,45,51,52,57,60,61,64], bioelectrical impedance [34,37,41,68,69], three- or four-site skinfolds [42,56,62], air displacement plethysmography (via BOD POD, Cosmed USA, Concord, CA, USA) [38], and deuterium oxide [32]. Notably, none of the studies used multi-compartment models to assess body composition.
Additional markers analyzed alongside anthropometrics and body composition included energetics (i.e., energy availability, intake, expenditure, and deficits) [32,34,39,57,59,60], metabolic health and metabolomics [34,45,51,52,60], nutritional status and dietary habits [33,53,59,61,62], physical fitness and athletic performance [22,33,34,37,38,40,41,42,49,50,53,55,57,61,66,68,69], physiological markers of health and stress (i.e., oxidative stress, systemic inflammation, reproductive health, bone health, and endocrine profile) [22,33,34,35,36,42,45,49,56,57,59,60,61,64,68], sleep [38,49,57], thermal strain [39], and psychological stress or mood state [49,50,51,52,53,66].
In general, body composition shifts were sensitive to tactical stressors, which led to either positive or negative impacts on anthropometric or body composition markers such as body mass and BMI, waist circumference, muscle mass/fat-free mass, BF/fat mass, and bone. Energy balance was one of the leading factors for how anthropometrics and body composition shifted around training. For example, tactical training events that included caloric restriction (in some cases severe) [32] combined with high energy expenditures were associated with high adrenal and oxidative stress, lower body weight, reduced bone formation, higher BF percentage, higher visceral adipose tissue, worsening metabolic health outcomes, decreased reproductive function, low energy availability (LEA) or nutrient-status symptoms, and/or higher systemic inflammation [32,33,35,36,45,49,53,56,57,59,60,64,66]. These effects were more pronounced among women entering training with a higher BMI. In contrast, tactical training events that resulted in positive body mass and body composition changes were associated with overall improvements in health, including (but not limited to) adequate energy availability, maintained or improved strength and power-based performance, and/or improved metabolic health and mood outcomes [51,55,61,62]. Overall, cardiorespiratory fitness and physical activity readiness assessment scores were associated with women’s body composition profile [41,42]. More specific to women’s health, women undergoing basic combat training on progestin-only contraceptives were found to have decreased bone mineral density and worsening bone health when compared to women on no contraceptive or the combined estrogen progestin oral contraceptive pill, but insight into these important interactions was only examined in one study [61]. Key body composition sex differences were observed. When compared to men, women tended to start military training with higher BF and lower muscle mass [57,69]. Women also tended to lose more total BF and/or preserve more muscle mass and maintain or regain lower body strength quicker compared to men undergoing the same tactical training [34,37,38,64,68].
3.4. Occupational Performance
This review included 21 studies (2,186 women; [Mean ± SD] age = 25 ± 5 y; BMI = 24.9 ± 1.8 kg/m2; BF = 29.4% ± 4.2%) that evaluated primary outcomes related to occupational performance in female tactical populations. Consistent with our other outcomes of interest, most studies focused on military settings (86%; 18 studies), and three focused on law enforcement [40,41,50]. The majority were conducted in military recruit or officer cadet cohorts (76%), with studies based in the U.S., United Kingdom, Israel, Norway, and South Korea. Only three studies involved a police population [40,41,50], and none were identified that assessed occupational performance in firefighting, EMS, or corrections populations. Notably, only one-third of studies (33%, seven studies) focused exclusively on women. See Table 4 for the individual summary of the coded dimensions for each study.
One-fourth (24%) of the included studies used a cross-sectional [33,41,47] or retrospective [40,50] design; the remaining studies were prospective cohort studies. Studies that examined occupational performance outcomes achieved “moderate” reporting quality (65.0% ± 8.3%) despite some variability in scores (52–81%), and only one study completely reported on ≥80% of checklist items (82.8%) [34].
Performance domains varied but commonly included anaerobic power (e.g., countermovement vertical jump), maximal force production (e.g., isometric mid-thigh pull, one-repetition maximum tests), military fitness assessments (e.g., Army physical fitness test, U.S. Marine Corps fitness tests), and tasks simulating tactical performance (e.g., casualty drag, water can carry, loaded march). Several studies [24,54,55] incorporated these field-based tasks along with assessment of physiological stress biomarkers (e.g., salivary cortisol). Eleven studies assessed body composition-related variables such as lean mass, fat mass, or BF percentage [33,34,37,38,41,42,56,57,61,68,69], while six studies reported BMI [22,40,49,50,53,55]. Notably, seven of the included studies assessed stress hormone concentrations in conjunction with performance outcomes [22,24,33,54,55,56,68]. Across studies, occupational performance metrics often declined during periods of high physiological strain, particularly under conditions of caloric deficit, sleep deprivation, or heavy cumulative training load, but generally recovered with adequate rest [57,68]. Only one study monitored recovery dynamics and contextual workload through wearable technology [55].
4. Discussion
The purpose of this scoping review was to synthesize the existing literature that comprehensively evaluated the impacts of stress on adrenal and neuroendocrine responses, body composition, and physical performance amongst women in demanding tactical occupations. A consistent theme was that occupation-related stress negatively impacted neuroendocrine, body composition, and performance outcomes. Sex differences in endocrine markers, energy metabolism, body composition profiles, and performance markers influenced the extent and manner by which tactical training impacted women. In addition to these contributions, this paper also provided key insights specific to the quality and reporting of studies in this research area. Notably, few studies achieved “high” reporting quality (no study achieved a perfect score), and on average, most were only considered to be of “moderate” reporting quality. For all studies included in this scoping review, one of the most poorly reported items was related to sample size determination (only nine studies completely reported on this item; see Table S3) [34,35,37,38,47,59,61,64,65]. The lack of sufficiently powered studies, with a high degree of reporting completeness, specific to women in tactical occupations, highlights a critical knowledge gap. The implications of our findings are summarized below, and when applicable, we have documented where knowledge is the weakest or poorly reported and have emphasized which research areas warrant additional investigation.
4.1. Adrenal Stress Response
The literature highlights both acute and chronic stress responses in women serving in tactical occupations. Tactical training courses are often designed to deliberately impose stress (i.e., stress inoculation), providing a controlled model to examine HPA axis and sympathoadrenal responses. Cortisol was consistently elevated in response to training stress, although longitudinal data suggest adaptive reductions in cortisol over time [52,54]. This potential adaptive response was also shown in two studies included in this review (Lieberman et al., 2012 [52]; Strahler et al., 2015 [65]). Sex differences in stress responses emerged across several studies. Women demonstrated heightened HPA axis sensitivity to adrenocorticotropic hormone stimulation [46], and cortisol remained elevated well into recovery after field exercises in female conscripts [68]. Cho et al. [36] reported alterations in reproductive hormones and stress-related neuropeptides during a 16-week officer training course, including decreases in estradiol and neuropeptide Y and increases in prolactin and cortisol, which corresponded with high rates of menstrual disruption. Further, we note the omission of estrogen as a marker of interest in studies evaluating stress response in women. Estrogen has been shown to modulate HPA axis activity in women, leading to heightened stress reactivity [23], which may help explain female-specific patterns of cortisol response.
Despite these insights, a major limitation of this literature is the absence of catecholamine measurement. Cortisol alone does not provide a complete picture of acute sympathoadrenal activity. Catecholamines (epinephrine, norepinephrine) are crucial for understanding short-term, SNS-driven stress responses, especially those linked to immediate operational performance. Their omission impairs the ability to evaluate the full spectrum of physiological stress responses. Several studies indirectly addressed the relationship between stress and performance. For instance, McFadden et al. [55] linked cortisol responses to physical performance metrics, but real-time integration of physiological and occupational performance data remains rare. Moreover, few studies considered environmental occupational stressors such as sleep deprivation, energy deficit, or urban exposure. Tomei et al. [67] observed higher testosterone concentrations in urban-exposed female police officers, potentially reflecting chronic environmental stress despite lacking cortisol or catecholamine data. Intersections between stress, metabolism, and immune function were noted in only a few studies. For example, Nindl et al. [56] found IGF-I concentrations increased while inflammatory markers decreased over the course of military basic training, suggesting positive adaptation. However, the role of stress hormone interactions (e.g., cortisol’s impact on IGF-I or immune function) was not evaluated. Conkright et al. [24] observed increased cortisol with suppressed growth hormone and IGF-I responses during a simulated operational stress protocol, supporting the need to study stress, metabolic, and immune interactions together. Furthermore, the reliance on salivary cortisol, while practical, presents limitations due to its high variability and lower specificity compared to plasma cortisol. A small number of studies used both methods, while only two incorporated alpha-amylase [31,65] as an index of psychological stress, despite its relevance.
4.2. Body Composition
Optimal body composition profiles, with an emphasis on supporting fat-free mass while maintaining healthy BF percentage, are hallmark components of the tactical athlete [70], leading to positive impacts on metabolic health [71], physical performance, and tactical occupation-specific tasks, such as load carriage, endurance, and strength [72]. Specific to women’s health, worsening body composition profiles are associated with reduced bone mineral density [73] and suboptimal reproductive function [74]. Body composition is highly energy and nutrient-sensitive, which was evident in the available literature, where muscle mass decreased in training environments that included particularly high energy expenditures, low quantity intake (caloric restriction/energy deficit), and/or low-quality nutrient intake. These outcomes were consistently associated with increased systemic inflammation, reduced metabolic health, and decreased performance, all of which led to negative impacts on readiness and resiliency.
A major observation in the current literature was the connection of energy balance to body composition profiles. The importance of energy balance was reflected in many of the LEA-related markers reported, such as decreased muscle mass, despite LEA itself not being a focal area for most of the studies. Traditionally, LEA has been most studied in the context of exercise and sport; however, women in tactical environments may be at increased risk for LEA and its downstream, deleterious consequences. A recent review by O’Leary et al. highlighted that LEA, common during intense field training, can trigger Relative Energy Deficiency in Sport (RED-S) in soldiers, which can lead to serious physiological and psychological sequelae [75]. Emphasizing this point, select studies in this review reported some of the more severe LEA phenotypes [76] such as reduced sleep quality, reduced reproductive function, training-induced anovulation [45], and poor bone metabolism [59]. Interestingly, these negative outcomes were observed in both acute and chronic training environments. Although LEA is typically discussed as a more chronic condition, even acute bouts of LEA (less than 5 days) can lead to physiological disruptions in women, such as negative impacts on metabolic health, musculoskeletal health, and hormonal profiles [76,77], and can eventually lead to reproductive health dysfunction. This is particularly relevant in tactical settings where undulating periods of highly stressful occupational demands combined with energy deficits may spiral into LEA. Indeed, Cho et al. [36] reported that a 16-week military training led to menstrual disruptions, including amenorrheic episodes for some women, coupled with hormonal changes, as has also been demonstrated by O’Leary and colleagues in their cross-sectional study of menstrual disturbances in British Service women [78]. These works underscore the broader physiological implications of LEA and the interconnectedness of training-specific stressors on anthropometrics, body composition, and reproductive health in women in tactical professions.
While LEA is composed of a series of physiological dysfunctions [79,80], it does not necessarily result in performance decrements [81,82], making it difficult to recognize. Identifying other objective and reliable markers to track LEA symptoms, such as body composition changes, is vital. Future research investigating how and to what extent chronic stress and energy deficits together negatively impact musculoskeletal health and body composition can help develop appropriate intervention strategies in this population. Furthermore, providing education on adequate energy availability, how to recognize LEA signs and symptoms, and offering a framework and solutions aimed at addressing LEA [79] is of great benefit to women in the tactical space, especially as women tend to be at higher risk for developing RED-S [83].
A unique theme in the available literature was women’s ability to preserve muscle mass and preferentially rely on adipose stores for energy (evidenced by BF percent changes with training), an advantage related to sex differences in energy metabolism. Several studies found that while women began training with a higher BF percentage, they tended to lose more BF and less muscle mass when compared to men [34,37,38,64,68]. One reason for this body composition shift may be due to women’s preferential reliance on fat for energy, specifically during exercise, reducing the need to turn to muscle breakdown for energy production [27]. Countless benefits are connected to maintaining muscle mass, emphasizing the importance of developing tactics aimed at supporting healthy body composition in this population. In addition to sustained performance, the ability to preserve and maintain skeletal muscle is closely tied to fatigue resiliency, improved metabolic (and overall) health, improved management of inflammation and oxidative stress, improved recovery processes [27], reduced injury risks [84], and improved cognitive function [85], all essential components of readiness. This observation opens the door for several different future research directions to better understand how to capitalize on women’s advantageous differences in energy metabolism. These include tactical-specific training and dietary approaches to support, maintain, and increase muscle mass, both in general settings and especially in adapting to stressful environments.
As expected, a wide range of methodologies were used in this body of work, with a mix of two- and three-compartment models used to assess body composition. Additionally, very few details were reported on the testing environment in which the assessments were collected. These inconsistencies bring an additional layer of consideration when comparing results across studies. Body composition assessments are highly sensitive to the testing environment, and results can be impacted by the assessment method itself, hydration state (i.e., dehydrated vs. euhydrated), nutrient status (i.e., fasting vs. postprandial) [86], environmental stress [87], medications (especially those that impact fluid balance), and more. It is also important to consider that body composition may be assessed in laboratory, clinical, and even field settings in this population, further introducing potential confounding variables that may impact results. Researchers should consider assessment tools that are valid, accurate, as well as feasible and appropriate for the testing environment. Future investigations may consider exploring how multi-compartment models for body composition can be included in this line of work, which would offer more precise and reliable assessments [88].
4.3. Occupational Performance
The literature on women’s occupational performance in tactical settings emphasizes assessments during recruit training or structured short-term courses. While these environments offer controlled opportunities to evaluate performance and adaptation, they do not fully capture operational readiness across the career lifespan or under real-world occupational demands. Load carriage emerged as a recurring and central theme in many studies (e.g., Conkright et al., 2021 [24]; O’Leary et al., 2023 [59]), reflecting its importance in military and first responder tasks. However, very few studies assessed how repeated or cumulative load carriage, especially under caloric or sleep deficits, impacts recovery and injury risk in women over time.
While some studies measured anaerobic power and task-specific performance, gold-standard strength assessments (e.g., one- or three-repetition maximum) were often absent, likely due to field testing constraints. This limits our understanding of absolute strength capacity and how it may support or constrain tactical readiness in women. In contrast, McFadden et al. [54] included both countermovement jumps and isometric mid-thigh pulls, paired with sleep, stress, and workload monitoring, offering a more complete view of performance under stress. Studies such as Vikmoen et al. [68] and Øfsteng et al. [57] show that women’s performance in anaerobic tasks declines in military training conditions but recovers with rest. However, recovery trajectories and resilience thresholds in female tactical personnel remain underexplored.
Perhaps most notably, few studies incorporated comprehensive physiological assessments, including stress markers, body composition, workload, and sleep data. McFadden et al. [54] and Conkright et al. [24] are exceptions, linking workload with hormonal and performance outcomes. Still, many studies did not evaluate key variables such as lean body mass or hormonal cycles, factors especially relevant to women’s performance and recovery. Preserving lean body mass is crucial in women. While women typically present lower baseline muscle mass, specific and personalized strength training programs can improve tactical occupation-relevant physical variables, including muscular strength and subsequent performance outcomes [89,90], supporting the need for comprehensive physiological assessments in this line of research. We also note a significant lack of data on women in non-military tactical populations. Indeed, no studies assessed occupational performance in firefighting (including wildland fire), EMS, or corrections. These settings involve unique demands (e.g., heat exposure, shift work, prolonged incident response) and may present sex-specific risk factors related to thermoregulation, cardiovascular strain, or reproductive suppression.
4.4. Limitations
Certain limitations must be applied to the current scoping review. First, we performed a critical appraisal of individual evidence to gauge the completeness of reporting (i.e., reporting quality) using existing checklists (e.g., The STROBE and CONSORT Checklists). Although not all scoping reviews include a critical appraisal of evidence, we acknowledge that our evaluation does not directly address methodological quality or risk of bias. Nonetheless, we posit that the quality and completeness of reporting by authors are related to higher quality and more robust research and are necessary for developing evidence-based recommendations. Importantly, we also note that a clear consensus on what tool, scale, or approach should constitute the ‘gold standard’ in assessing the quality of evidence included in scoping reviews has yet to emerge [28], particularly for research involving tactical occupations. Another potential limitation is that our search strategy may not have identified all potentially eligible sources of evidence despite using multiple databases and platforms. However, given the paucity of data involving women in tactical occupations, we are confident that we have identified the relevant research aligned with the objectives of this scoping review. Finally, the sheer volume of literature (or lack thereof) that explicitly examines the unique physiological and performance-related demands placed on women in tactical occupations is a major limitation of the literature, beyond this scoping review. While there has been progress in this regard, there are persistent critical gaps that must be addressed.
One of the major limitations of this line of research is the lack of female reproductive health insight despite its connection to the adrenal/neuroendocrine system, energy balance and body composition, and physical performance outcomes. This was a uniformly identified gap in the research studies included in this review. Most studies failed to incorporate, and much less stratify by, information on contraception use and/or type, menstrual cycle phase details, reproductive health state (i.e., menstruating, pregnant, peri-menopausal, or menopausal), or reproductive health insights in general (amenorrheic, menstrual cycle dysfunction, reproductive hormone disruption, etc.). Including reproductive health data would provide much-needed context for the observed stress-influenced outcomes. While incorporating reproductive health measures is not yet standard practice in the field, recent works have commented on the critical need to include female reproductive health markers, properly identify reproductive health stage, and track menstrual cycle phase to strengthen female athlete research [91]. This need extends to female tactical populations, as military training has been associated with marked reproductive and menstrual cycle dysfunction [92]. Future research that includes both subjective and objective measures associated with reproductive physiology is desperately needed.
4.5. Evidence-Informed Recommendations for Future Research
The available research lays the groundwork for a wide span of future directions investigating the impact of stress on female physiology, body composition, and performance amongst women in tactical occupations. Future research must characterize women’s overall health, body composition, fitness, and performance profiles in tactical domains in depth. Even more pressing, research must explore how women’s profiles shift in both acute and chronic stressful tactical environments. This comprehensive approach allows for broader contextual insight into the unique phenotypes associated with women in tactical occupations and more closely identifies areas of both strength and concern for more targeted discoveries. For example, works investigating how adrenal and neuroendocrine biomarkers, such as catecholamines, shift with occupational stress and potentially impact metabolic and immune responses would add much-needed depth relative to the available cortisol data in this population. The inclusion of more specific and robust assessment techniques such as body composition measurements that include multi-compartment models and surveying LEA, its associated risk factors, and RED-S incidences would further strengthen this line of work. Targeted interventions specific to women in tactical occupations should address energy and nutrient deficiencies [26] and include structured physical fitness and strength and conditioning approaches aimed at supporting and enhancing skeletal muscle mass specific to women in tactical occupations [93,94,95]. Future research specific to tactical women must incorporate key measures associated with occupational readiness and should be aimed at a comprehensive understanding of the relationship between resiliency, muscle mass, and women’s health. These areas can, and must be, combined with comprehensive reproductive health assessments that include both objective and subjective measures. Finally, ample opportunity lies in expanding tactical research beyond military populations to other tactical domains where we know far less, such as firefighting, EMS, and corrections. While some domain-specific challenges in this space have been identified, the breadth and depth of this area of research is severely lacking. Addressing these knowledge gaps would provide much benefit and further emphasize awareness and understanding of occupation-specific demands and stressors. Our current understanding of the impact of stress on adrenal and neuroendocrine responses, body composition, and performance amongst women within each tactical domain and the areas for future research in these tactical spaces are summarized in Figure 3.
Figure 3.
Known responses to occupational stressors within each tactical domain and directions for future research regarding female tactical athletes. We note the lack of data specific to women in the corrections tactical domain, highlighting this domain’s importance for future research directions. EMS, Emergency Medical Services. SWAT, Special Weapons and Tactics unit. This image was created using Procreate® (version 5.3.15) and PowerPoint (version 2.98.4).
5. Conclusions
This scoping review highlights the progress in evaluating how stress affects occupational performance in women serving in tactical roles, but our understanding remains incomplete due to methodological and conceptual limitations in the literature. The extent of the consensus found 40 studies of moderate reporting quality with overarching themes focused on how stress dysregulates the HPA axis, has mixed effects on body composition, with most as adverse, and results in performance declines, particularly under heavy external loads and energy deficits. Current studies emphasize early-career military cohorts and field-based testing methods, with limited integration of comprehensive physiological monitoring or stress–response data. Cortisol, while widely used as a measure of adrenal stress response, cannot substitute for a comprehensive assessment of sympathoadrenal activity, especially in the absence of catecholamine measurement and physical performance correlation. While body composition is closely associated with tactical health, performance, and recovery outcomes, assessment discrepancies, coupled with a lack of dietary intake and energy expenditure insight, result in conflicting outcomes and an incomplete understanding of this performance metric relative to women’s tactical performance. Findings specific to occupational performance suggest that anaerobic power and task-specific performance decline under stress but may recover with appropriate rest. Lean body mass likely contributes to performance potential, yet its role is underassessed.
Key gaps include a lack of integration of sympathoadrenal stress responses (i.e., catecholamines) and evaluation of associated metabolic and immune responses, underrepresentation of female-specific hormonal and reproductive health measures, limited contextualization of stress responses in operational settings (e.g., sleep deprivation or energy deficit), and sparse linkage between stress biomarkers and occupational readiness or injury outcomes.
As women comprise a growing proportion of tactical professionals, including military, police, fire service, EMS, and corrections, tailored research is needed to address their unique physiological demands [96]. Holistic research strategies are needed to capture the complexity of performance readiness in women, integrating stress and muscle physiology, reproductive health, energy and nutrient balance, and resilience in realistic operational contexts. Comprehensive assessment of these interrelated aspects of performance readiness addresses current knowledge gaps and is vital for informing policy, improving readiness, and enhancing the health and career longevity of female tactical personnel.
Abbreviations
The following abbreviations are used in the main text of the manuscript:
| BF | Body fat |
| BM | Body mass |
| BMI | Body mass index |
| BMM | Bone mineral mass |
| CCP | Combined contraceptive pill |
| CFT | Combat fitness test |
| CK | Creatine kinase |
| CMJ | Countermovement jump |
| CMJREL | CMJ relative to body mass |
| COCP | Combined oral contraceptive |
| CRH | Corticotropin-releasing hormone |
| CRP | C-reactive protein |
| CTT-2 | Color trails test |
| CTx | C-telopeptide cross-links of type I collagen |
| DBP | Diastolic blood pressure |
| DHEA | Dihydroepiandrostenedione |
| DHEA-S | Dihydroepiandrostenedione sulfate |
| DLM | Dry lean mass |
| DLW | Doubly labeled water |
| DXA | Dual energy X-ray absorptiometry |
| EEREL | Energy expenditure relative to body mass |
| EMS | Emergency medical services |
| F | Female |
| FAI | Free androgen index |
| FFA | Free fatty acids |
| FFM | Fat-free mass |
| FM | Fat mass |
| FSH | Follicle-stimulating hormone |
| GnRH | Gonadotropin-releasing hormone |
| GSH | Glutathione |
| GPX | Glutathione peroxidase |
| HCC | Hair cortisol concentration |
| HDL | High-density lipoprotein |
| HOMA2 IR | Homeostatic modeling assessment of insulin resistance 2 |
| HPA | Hypothalamic–pituitary–adrenal |
| HPG | Hypothalamic–pituitary–gonadal |
| HPO | Hypothalamic–pituitary–ovarian |
| HR | Heart rate |
| HRV | Heart rate variability |
| IFN-γ | Interferon γ |
| IGF-1 | Insulin-like growth factor |
| LEA | Low energy availability |
| PRISMA-ScR | Preferred Reporting Items for Systematic Review and Meta-Analyses extension for Scoping Reviews |
| REDs | Relative Energy Deficiency in Sport |
| SD | Standard deviation |
| SNS | Sympathetic nervous system |
| U.S. | United States |
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/metabo15080506/s1. Table S1. Full search strategy used for each electronic database; Table S2. Description of potentially eligible studies that were excluded from the final sample following full-text review (n = 64); Table S3. Reporting completeness for individual checklist items (expressed as a percentage of items completely reported) for the total sample of included studies and each outcome of interest. References [92,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,148,149,150,151,152,153,154,155,156,157] are cited in the supplementary materials.
Author Contributions
Conceptualization, design, and project management, T.K.S., H.V.M., and C.S.; key search terms: T.K.S., H.V.M., and C.S.; scoping review approach, database search, data extraction, and data management: E.A.S. and H.V.M.; table design and management: E.A.S. and H.V.M.; critical evaluation of and approvals for each article: led by E.A.S. and H.V.M. with input from T.K.S. and C.S.; data extraction and quantitative summaries: E.A.S. and H.V.M.; writing—original draft preparation, all authors; writing—review and editing, all authors; visualization, E.A.S. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
All reported studies/experiments with human or animal participants have been previously published and complied with all applicable ethical standards (i.e., Helsinki Declaration and its amendments, institutional/national research committee standards, and guidelines).
Data Availability Statement
All reported studies/experiments have been previously published with available data to support findings.
Conflicts of Interest
The authors declare no conflicts of interest.
Funding Statement
This research received no external funding.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
References
- 1.Washington D.L., Farmer M.M., Mor S.S., Canning M., Yano E.M. Assessment of the healthcare needs and barriers to VA use experiences by women veterans: Findings from the national survey of women Veterans. Med. Care. 2015;53:S23–S31. doi: 10.1097/MLR.0000000000000312. [DOI] [PubMed] [Google Scholar]
- 2.Korhonen V. Gender Distribution of Full-Time U.S. Law Enforcement Employees in the United States in 2023. 2024. [(accessed on 29 May 2024)]. Available online: https://www.statista.com/statistics/195324/gender-distribution-of-full-time-law-enforcement-employees-in-the-us/
- 3.McClung H.L., Spiering B.A., Bartlett P.M., Walker L.A., Lavoie E.M., Sanford D.P., Friedl K.E. Physical and physiological characterization of female elite warfighters. Med. Sci. Sports Exerc. 2022;54:1527–1533. doi: 10.1249/MSS.0000000000002942. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Hendel E., MacEachern K.H., Haxhiu A., Waruszynski B.T. “Proud, brave, and tough”: Women in the Canadian combat arms. Front. Sociol. 2024;9:1304075. doi: 10.3389/fsoc.2024.1304075. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Lesniak A.Y., Bergstrom H.C., Clasey J.L., Stromberg A.J., Abel M.G. The effect of personal protective equipment on firefighter occupational performance. J. Strength Cond. Res. 2020;34:2165–2172. doi: 10.1519/JSC.0000000000003384. [DOI] [PubMed] [Google Scholar]
- 6.Lockie R.G., Dawes J.J., Kornhauser C.L., Holmes R.J. Cross-sectional and retrospective cohort analysis of the effects of age on flexibility, strength endurance, lower-body power, and aerobic fitness in law enforcement officers. J. Strength Cond. Res. 2019;33:451–458. doi: 10.1519/JSC.0000000000001937. [DOI] [PubMed] [Google Scholar]
- 7.Joseph A., Wiley A., Orr R.M., Schram B., Dawes J.J. The impact of load carriage on measures of power and agility in tactical occupations: A critical review. Int. J. Environ. Res. Public Health. 2018;15:88. doi: 10.3390/ijerph15010088. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Hwang J., Chong N.-S., Zhang M., Agnew R.J., Xu C., Li Z., Xu X. Face-to-face with scorching wildfire: Potential toxicant exposure and the health risks of smoke for wildland firefighters at the wildland-urban interface. Lancet Reg. Health Am. 2023;21:100482. doi: 10.1016/j.lana.2023.100482. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Li B., Xu Y., Wang D., Wei B., Zhu H., Wu M., Lan X., Yin Q., Cao Y. High-altitude acute hypoxia endurance and comprehensive lung function in pilots. Aerosp. Med. Hum. Perform. 2025;96:191–197. doi: 10.3357/AMHP.6551.2025. [DOI] [PubMed] [Google Scholar]
- 10.Martin K., McLeod E., Périard J., Rattray B., Keegan R., Pyne D.B. The impact of environmental stress on cognitive performance: A systematic review. Hum. Factors. 2019;61:1205–1246. doi: 10.1177/0018720819839817. [DOI] [PubMed] [Google Scholar]
- 11.Schafer E.A., Chapman C.L., Castellani J.W., Looney D.P. Energy expenditure during physical work in cold environments: Physiology and performance considerations for military service members. J. Appl. Physiol. 2024;137:995–1013. doi: 10.1152/japplphysiol.00210.2024. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Dyal M.-A.A., Smith T.D., DeJoy D.M., Moore B.A. Occupational stress and burnout in the fire service: Examining the complex role and impact of sleep health. Behav. Modif. 2022;46:374–394. doi: 10.1177/01454455211040049. [DOI] [PubMed] [Google Scholar]
- 13.Purba A., Demou E. The relationship between organisational stressors and mental well-being within police officers: A systematic review. BMC Public Health. 2019;19:1286. doi: 10.1186/s12889-019-7609-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Violanti J.M., Charles L.E., McCanlies E., Hartley T.A., Baughman P., Andrew M.E., Fekedulegn D., Ma C.C., Mnatsakanova A., Burchfiel C.M. Police stressors and health: A state-of-the-art review. Polic. Int. J. Police Strateg. Manag. 2017;40:642–656. doi: 10.1108/PIJPSM-06-2016-0097. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Allison P., Tiesman H.M., Wong I.S., Bernzweig D., James L., James S.M., Navarro K.M., Patterson P.D. Working hours, sleep, and fatigue in the public safety sector: A scoping review of the research. Am. J. Ind. Med. 2022;65:878–897. doi: 10.1002/ajim.23407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Lawn S., Roberts L., Willis E., Couzner L., Mohammadi L., Goble E. The effects of emergency medical service work on the psychological, physical, and social well-being of ambulance personnel: A systematic review. BMC Psychiatry. 2020;20:348. doi: 10.1186/s12888-020-02752-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Angehrn A., Fletcher A.J., Carleton R.N. “Suck it up, buttercup”: Understanding and overcoming gender disparities in policing. Int. J. Environ. Res. Public Health. 2021;18:7627. doi: 10.3390/ijerph18147627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Ilias M., Riach K., Demou E. Understanding the interplay between organisational injustice and the health and wellbeing of female police officers: A meta-ethnography. BMC Public Health. 2024;24:2659. doi: 10.1186/s12889-024-20152-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Kimerling R., Street A.E., Pavao J., Smith M.W., Cronkite R.C., Holmes T.H., Frayne S.M. Military-related sexual trauma among Veterans Health Administration patients returning from Afghanistan and Iraq. Am. J. Public Health. 2010;100:1409–1412. doi: 10.2105/AJPH.2009.171793. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Selye H. Stress and the general adaptation syndrome. Br. Med. J. 1950;1:1383–1392. doi: 10.1136/bmj.1.4667.1383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Corrigan S.L., Roberts S., Warmington S., Drain J., Main L.C. Monitoring stress and allostatic load in first responders and tactical operators using heart rate variability: A systematic review. BMC Public Health. 2021;21:1701. doi: 10.1186/s12889-021-11595-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Szivak T.K., Lee E.C., Saenz C., Flanagan S.D., Focht B.C., Volek J.S., Maresh C.M., Kraemer W.J. Adrenal stress and physical performance during military survival training. Aerosp. Med. Hum. Perform. 2018;89:99–107. doi: 10.3357/AMHP.4831.2018. [DOI] [PubMed] [Google Scholar]
- 23.Goel N., Workman J.L., Lee T.T., Innala L., Viau V. Sex differences in the HPA axis. Compr. Physiol. 2014;4:1121–1155. doi: 10.1002/j.2040-4603.2014.tb00575.x. [DOI] [PubMed] [Google Scholar]
- 24.Conkright W.R., Beckner M.E., Sinnott A.M., Eagle S.R., Martin B.J., Lagoy A.D., Proessl F., Lovalekar M., Doyle T.L.A., Agostinelli P., et al. Neuromuscular performance and hormonal responses to military operational stress in men and women. J. Strength Cond. Res. 2021;35:1296–1305. doi: 10.1519/JSC.0000000000004013. [DOI] [PubMed] [Google Scholar]
- 25.Pierce J.R., Martin B.J., Rarick K.R., Alemany J.A., Staab J.S., Kraemer W.J., Hymer W.C., Nindl B.C. Growth hormone and insulin-like growth factor I molecular weight isoform responses to resistance exercise are sex-dependent. Front. Endocrinol. 2020;11:571. doi: 10.3389/fendo.2020.00571. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Gonzalez D.E., McAllister M.J., Waldman H.S., Ferrando A.A., Joyce J.M., Barringer N.D., Dawes J.J., Kieffer A.J., Harvey T., Kerksick C.M., et al. International society of sports nutrition position stand: Tactical athlete nutrition. J. Int. Soc. Sports Nutr. 2022;19:267–315. doi: 10.1080/15502783.2022.2086017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Sanchez B.N., Volek J.S., Kraemer W.J., Saenz C., Maresh C.M. Sex differences in energy metabolism: A female-oriented discussion. Sports Med. 2024;54:2033–2057. doi: 10.1007/s40279-024-02063-8. [DOI] [PubMed] [Google Scholar]
- 28.Tricco A.C., Lillie E., Zarin W., O’Brien K.K., Colquhoun H., Levac D., Moher D., Peters M.D.J., Horsley T., Weeks L., et al. PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation. Ann. Intern. Med. 2018;169:467–473. doi: 10.7326/M18-0850. [DOI] [PubMed] [Google Scholar]
- 29.von Elm E., Altman D.G., Egger M., Pocock S.J., Gøtzsche P.C., Vandenbroucke J.P., Initiative S. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: Guidelines for reporting observational studies. J. Clin. Epidemiol. 2008;61:344–349. doi: 10.1016/j.jclinepi.2007.11.008. [DOI] [PubMed] [Google Scholar]
- 30.Hopewell S., Chan A.W., Collins G.S., Hróbjartsson A., Moher D., Schulz K.F., Tunn R., Aggarwal R., Berkwits M., Berlin J., et al. CONSORT 2025 statement: Updated guideline for reporting randomised trials. Br. Med. J. 2015;388:e081123. doi: 10.1136/bmj-2024-081123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.McGraw L.K., Out D., Hammermeister J.J., Ohlson C.J., Pickering M.A., Granger D.A. Nature, correlates, and consequences of stress-related biological reactivity and regulation in Army nurses during combat casualty simulation. Psychoneuroendocrinology. 2013;38:135–144. doi: 10.1016/j.psyneuen.2012.05.009. [DOI] [PubMed] [Google Scholar]
- 32.Ahmed M., Mandic I., Desilets E., Smith I., Sullivan-Kwantes W., Jones P.J., Goodman L., Jacobs I., L’Abbé M. Energy balance of Canadian Armed Forces personnel during an arctic-like field training exercise. Nutrients. 2020;12:1638. doi: 10.3390/nu12061638. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Andrews A.M., Kantor M.A. Oxidative stress increases in overweight individuals following an exercise test. Mil. Med. 2010;175:1014–1019. doi: 10.7205/MILMED-D-09-00155. [DOI] [PubMed] [Google Scholar]
- 34.Beckner M.E., Thompson L., Radcliffe P.N., Cherian R., Wilson M., Barringer N., Margolis L.M., Karl J.P. Sex differences in body composition and serum metabolome responses to sustained, physical training suggest enhanced fat oxidation in women compared with men. Physiol. Genom. 2023;55:235–247. doi: 10.1152/physiolgenomics.00180.2022. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Charles L.E., Burchfiel C.M., Violanti J.M., Fekedulegn D., Slaven J.E., Browne R.W., Hartley T.A., Andrew M.E. Adiposity measures and oxidative stress among police officers. Obesity. 2008;16:2489–2497. doi: 10.1038/oby.2008.395. [DOI] [PubMed] [Google Scholar]
- 36.Cho G.J., Han S.W., Shin J.-H., Kim T. Effects of intensive trainng on menstrual function and certain serum hormones and peptides related to the female reproductive system. Medicine. 2017;96:e6876. doi: 10.1097/MD.0000000000006876. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Coge M., Neiva H.P., Pereira A., Faíl L., Ribeiro B., Esteves D. Effects of 34 weeks of military service on body composition and physical fitness in military cadets of Angola. J. Funct. Morphol. Kinesiol. 2024;9:111. doi: 10.3390/jfmk9030111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Conkright W.R., Beckner M.E., Sahu A., Mi Q., Clemens Z.J., Lovalekar M., Flanagan S.D., Martin B.J., Ferrarelli F., Ambrosio F., et al. Men and women display dinstinct extracellular vesicle biomarker signatures in response to military operational stress. J. Appl. Physiol. 2022;132:1125–1136. doi: 10.1152/japplphysiol.00664.2021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Cuddy J.S., Sol J.A., Hailes W.S., Ruby B.C. Work patterns dictate energy demands and thermal strain during wildland firefighting. Wild Environ. Med. 2015;26:221–226. doi: 10.1016/j.wem.2014.12.010. [DOI] [PubMed] [Google Scholar]
- 40.Dawes J.J., dos Santos M.L., Kornhauser C., Holmes R.J., Alvar B.A., Lockie R.G., Orr R.M. Longitudinal changes in health and fitness measures among state patrol officers by sex. J. Strength Cond. Res. 2023;37:881–886. doi: 10.1519/JSC.0000000000004327. [DOI] [PubMed] [Google Scholar]
- 41.Dicks N.D., Shoemaker M.E., DeShaw K.J., Carper M.J., Hackney K.J., Barry A.M. Contributions from incumbent police officer’s physical activity and body composition to occupational assessment performance. Front. Public Health. 2023;11:1217187. doi: 10.3389/fpubh.2023.1217187. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Evans R.K., Antczak A.J., Lester M., Yanovich R., Israeli E., Moran D.S. Effects of a 4-month recruit training program on markers of bone metabolism. Med. Sci. Sports Exerc. 2008;40:S660–S670. doi: 10.1249/MSS.0b013e318189422b. [DOI] [PubMed] [Google Scholar]
- 43.Flegr J., Hampl R., Černochová D., Preiss M., Bičíková M., Sieger L., Příplatová L., Kaňková Š., Klose J. The relation of cortisol and sex hormone levels to results of psychological, performance, IQ and memory tests in military men and women. Neuroendocrinol. Lett. 2012;33:224–235. [PubMed] [Google Scholar]
- 44.Gifford R.M., O’Leary T.J., Double R.L., Wardle S.L., Wilson K., Boyle L.D., Homer N.Z.M., Kirschbaum C., Greeves J.P., Woods D., et al. Positive adaptation of HPA axis function in women during 44 weeks of infantry-based military training. Psychoneuroendocrinology. 2019;110:104432. doi: 10.1016/j.psyneuen.2019.104432. [DOI] [PubMed] [Google Scholar]
- 45.Gifford R.M., O’Leary T.J., Wardle S.L., Double R.L., Homer N.Z.M., Howie A.F., Greeves J.P., Anderson R.A., Woods D., Reynolds R.M. Reproductive and metabolic adaptation to multistressor training in women. Am. J. Physiol. Endocrinol. Metab. 2021;321:E281–E291. doi: 10.1152/ajpendo.00019.2021. [DOI] [PubMed] [Google Scholar]
- 46.Gifford R.M., O’Leary T.J., Knight R.L., Wardle S.L., Doig C.L., Anderson R.A., Greeves J.P., Reynolds R.M., Woods D. Sex-related hypothalamic-pituitary-gonadal and hypothalamic-pituitary-adrenal axis adaptation during military training. J. Appl. Physiol. 2025;138:13–21. doi: 10.1152/japplphysiol.00691.2024. [DOI] [PubMed] [Google Scholar]
- 47.Greer J.A., Heye K.R., McGlynn A., Johansson S., Vaccaro C.M. Association of pelvic floor disorders, perceived psychological stress, and military service in U.S. Navy servicewomen: A cross-sectional survey. Urogynecology. 2023;29:966–973. doi: 10.1097/SPV.0000000000001374. [DOI] [PubMed] [Google Scholar]
- 48.Johnsen A.M., Theodorsson E., Broström A., Wagman P., Fransson E.I. Work-related factors and hair cortisol concentrations among men and women in emergency medical services in Sweden. Sci. Rep. 2023;13:12877. doi: 10.1038/s41598-023-40076-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Kargl C.K., Gage C.R., Forse J.N., Koltun K.J., Bird M.B., Lovalekar M., Martin B.J., Nindl B.C. Inflammatory and oxidant responses to arduous military training: Associations with stress, sleep, and performance. Med. Sci. Sports Exerc. 2024;56:2315–2327. doi: 10.1249/MSS.0000000000003525. [DOI] [PubMed] [Google Scholar]
- 50.Krugly S., Bjärsholm D., Jansson A., Hansen A.R., Hansson O., Brehm K., Datmo A., Östenberg A.H., Vikman J. A retrospective study of physical fitness and mental health among police students in Sweden. Police J. Theory Pract. Princ. 2023;96:430–450. doi: 10.1177/0032258X221089576. [DOI] [Google Scholar]
- 51.Lieberman H.R., Kellogg M.D., Bathalon G.P. Female Marine recruit training: Mood, body composition, and biochemical changes. Med. Sci. Sports Exerc. 2008;40:S671–S676. doi: 10.1249/MSS.0b013e31818943b3. [DOI] [PubMed] [Google Scholar]
- 52.Lieberman H.R., Kellog M.D., Kramer F.M., Bathalon G.P. Lipid and other plasma markers are associated with anxiety, depression, and fatigue. Health Psychol. 2012;31:210–216. doi: 10.1037/a0026499. [DOI] [PubMed] [Google Scholar]
- 53.McClung J.P., Karl J.P., Cable S.J., Williams K.W., Nindl B.C., Young A.J., Lieberman H.R. Randomized, double-blind, placebo-controlled trial of iron supplementation in female soldiers during military training: Effects on iron status, physical performance, and mood. Am. J. Clin. Nutr. 2009;90:124–131. doi: 10.3945/ajcn.2009.27774. [DOI] [PubMed] [Google Scholar]
- 54.McFadden B.A., Cintineo H.P., Chandler A.J., Mastrofini G.F., Vincenty C.S., Peterson P., Lovalekar M., Nindl B.C., Arent S.M. A sex comparison of the physical and physiological demands of United States Marine Corps recruit training. Mil. Med. 2024;189:74–83. doi: 10.1093/milmed/usae071. [DOI] [PubMed] [Google Scholar]
- 55.McFadden B.A., Cintineo H.P., Chandler A.J., Peterson P., Lovalekar M., Nindl B.C., Arent S.M. United States Marine Corps recruit training demands associated with performance outcomes. Mil. Med. 2024;189:84–93. doi: 10.1093/milmed/usae124. [DOI] [PubMed] [Google Scholar]
- 56.Nindl B.C., Scofield D.E., Strohbach C.A., Centi A.J., Evans R.K., Yanovich R., Moran D.S. IGF-I, IGFBPs, and inflammatory cytokine responses during gender-integrated Israeli Army basic combat training. J. Strength Cond. Res. 2012;26:S73–S81. doi: 10.1519/JSC.0b013e31825d81ba. [DOI] [PubMed] [Google Scholar]
- 57.Øfsteng S.J., Garthe I., Jøsok Ø., Knox S., Helkala K., Knox B., Ellefsen S., Rønnestad B.R. No effect of increasing protein intake during military exercise with severe energy deficit on body composition and performance. Scand. J. Med. Sci. Sports. 2020;30:865–877. doi: 10.1111/sms.13634. [DOI] [PubMed] [Google Scholar]
- 58.O’Leary T.J., Saunders S.C., McGuire S.J., Izard R.M. Sex differences in neuromuscular fatigability in response to load carriage in British Army recruits. J. Sci. Med. Sport. 2018;21:591–595. doi: 10.1016/j.jsams.2017.10.018. [DOI] [PubMed] [Google Scholar]
- 59.O’Leary T.J., Coombs C.V., Edwards V.C., Blacker S.D., Knight R.L., Koivula F.N., Tang J.C.Y., Fraser W.D., Wardle S.L., Greeves J.P. The effect of sex and protein supplementation on bone metabolism during 36-h military field exercise in energy deficit. J. Appl. Physiol. 2023;134:1481–1495. doi: 10.1152/japplphysiol.00106.2023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.O’Leary T.J., Gifford R.M., Knight R.L., Wright J., Handford S., Venables M.C., Reynolds R.M., Woods D., Wardle S.L., Greeves J.P. Sex differences in energy balance, body composition, and metabolic and endocrine markers during prolonged arduous military training. J. Appl. Physiol. 2024;136:938–948. doi: 10.1152/japplphysiol.00864.2023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.O’Leary T.J., Evans H.A., Close M.-E.O., Izard R.M., Walsh N.P., Coombs C.V., Carswell A.T., Oliver S.J., Tang J.C.Y., Fraser W.D., et al. Hormonal contraceptive use and physical performance, body composition, and musculoskeletal injuries during military training. Med. Sci. Sports Exerc. 2025;57:613–624. doi: 10.1249/MSS.0000000000003588. [DOI] [PubMed] [Google Scholar]
- 62.Pasiakos S.M., Karl J.P., Lutz L.J., Murphy N.E., Margolis L.M., Rood J.C., Williams K.W., Young A.J., McClung J.P. Cardiometabolic risk in US Army recruits and the effects of basic combat training. PLoS ONE. 2012;7:e31222. doi: 10.1371/journal.pone.0031222. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Margolis L.M., Pasiakos S.M., Karl J.P., Rood J.C., Cable S.J., Williams K.W., Young A.J., McClung J.P. Differential effects of military training on fat-free mass and plasma amino acid adaptations in men and women. Nutrients. 2012;4:2035–2046. doi: 10.3390/nu4122035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Popp K.L., Bozzini B.N., Reynoso M., Coulombe J., Guerriere K.I., Proctor S.P., Castellani C.M., Walker L.A., Zurinaga N., Kuhn K., et al. Hypothalamic-pituitary-ovarian axis suppression is common among women during US Army Basic Combat Training. Br. J. Sports Med. 2024;58:1052–1060. doi: 10.1136/bjsports-2023-107716. [DOI] [PubMed] [Google Scholar]
- 65.Strahler J., Ziegert T. Psychobiological stress response to a simulated school shooting in police officers. Psychoneuroendocrinology. 2015;51:80–91. doi: 10.1016/j.psyneuen.2014.09.016. [DOI] [PubMed] [Google Scholar]
- 66.Szivak T.K., Thomas M.M., Pietrzak R.H., Nguyen D.R., Ryan D.M., Mazure C.M. Obesity risk among West Point graduates later in life. J. Strength Cond. Res. 2023;37:1284–1291. doi: 10.1519/JSC.0000000000003824. [DOI] [PubMed] [Google Scholar]
- 67.Tomei G., Ciarrocca M., Fiore P., Rosati M.V., Pimpinella B., Anzani M.F., Giubilati R., Cangemi C., Tomao E., Tomei F. Exposure to urban stressor and effects on free testosterone in female workers. Sci. Total Environ. 2008;392:198–202. doi: 10.1016/j.scitotenv.2007.12.007. [DOI] [PubMed] [Google Scholar]
- 68.Vikmoen O., Teien H.K., Raustøl M., Aandstad A., Tansø R., Gulliksrud K., Skare M., Raastad T. Sex differences in the physiological response to a demanding military field exercise. Scand. J. Med. Sci. Sports. 2020;30:1348–1359. doi: 10.1111/sms.13689. [DOI] [PubMed] [Google Scholar]
- 69.Zurek G., Lenart D., Lachowicz M., Zebrowski K., Jamro D. Factors influencing the executive functions of male and female cadets. Int. J. Environ. Res. Public Health. 2022;19:17043. doi: 10.3390/ijerph192417043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Cialdella-Kam L., Bloedon T.K., Stone M.S. Body composition as a marker of performance and health in military personnel. Front. Sports Act. Living. 2023;5:1223254. doi: 10.3389/fspor.2023.1223254. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Saenz C., Hooper S., Orange T., Knight A., Barragan M., Lynch T., Remenapp A., Coyle K., Winters C., Hausenblas H. Effect of a free-living ketogenic diet on feasibility, satiety, body composition, and metabolic health in women: The grading level of optimal carbohydrate for women (GLOW) study. J. Am. Coll. Nutr. 2021;40:295–306. doi: 10.1080/07315724.2021.1875338. [DOI] [PubMed] [Google Scholar]
- 72.Harty P.S., Friedl K.E., Nindl B.C., Harry J.R., Vellers H.L., Tinsley G.M. Military body composition standards and physical performance: Historical perspectives and future directions. J. Strength Cond. Res. 2022;36:3551–3561. doi: 10.1519/JSC.0000000000004142. [DOI] [PubMed] [Google Scholar]
- 73.Mallinson R.J., Williams N.I., Hill B.R., De Souza M.J. Body composition and reproductive function exert unique influences on indices of bone health in exercising women. Bone. 2013;56:91–100. doi: 10.1016/j.bone.2013.05.008. [DOI] [PubMed] [Google Scholar]
- 74.Chapman C.L., Giersch G.E.W., Gwin J.A., Goldenstein S., Schafer E.A., Roberts B.M., Potter A.W. Body composition and physical readiness in military servicemembers: Cross-disciplinary advances and current challenges. Exerc. Sport. Mov. 2025;3:e00050. doi: 10.1249/ESM.0000000000000050. [DOI] [Google Scholar]
- 75.O’Leary T.J., Wardle S.L., Greeves J.P. Energy deficiency in soldiers: The risk of the Athlete Triad and Relative Energy Deficiency in Sport syndromes in the military. Front. Nutr. 2020;7:142. doi: 10.3389/fnut.2020.00142. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Cabre H.E., Moore S.R., Smith-Ryan A.E., Hackney A.C. Relative Energy Deficiency in Sport (RED-S): Scientific, clinical, and practical implications for the female athlete. Dtsch. Z. Sportmed. 2022;73:225–234. doi: 10.5960/dzsm.2022.546. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Popp K.L., Cooke L.M., Bouxsein M.L., Hughes J.M. Impact of low energy availability on skeletal health in physically active adults. Calcif. Tissue Int. 2022;110:605–614. doi: 10.1007/s00223-022-00957-1. [DOI] [PubMed] [Google Scholar]
- 78.O’Leary T.J., Perrett C., Coombs C.V., Double R.L., Keay N., Wardle S.L., Greeves J.P. Menstrual disturbances in British Servicewomen: A cross-sectional observational study of prevalence and risk factors. Front. Nutr. 2022;9:984541. doi: 10.3389/fnut.2022.984541. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 79.Mountjoy M., Sundgot-Borgen J., Burke L., Carter S., Constantini N., Lebrun C., Meyer N., Sherman R., Steffen K., Budgett R., et al. The IOC consensus statement: Beyond the Female Athlete Triad--Relative Energy Deficiency in Sport (RED-S) Br. J. Sports Med. 2014;48:491–497. doi: 10.1136/bjsports-2014-093502. [DOI] [PubMed] [Google Scholar]
- 80.Burke L.M., Ackerman K.E., Heikura I.A., Hackney A.C., Stellingwerff T. Mapping the complexities of Relative Energy Deficiency in Sport (REDs): Development of a physiological model by a subgroup of the International Olympic Committee (IOC) Consensus on REDs. Br. J. Sports Med. 2023;57:1098–1108. doi: 10.1136/bjsports-2023-107335. [DOI] [PubMed] [Google Scholar]
- 81.Hooper D.R., Mallard J., Wight J.T., Conway K.L., Pujalte G.G.A., Pontius K.M., Saenz C., Hackney A.C., Tenforde A.S., Ackerman K.E. Performance and health decrements associated with Relative Energy Deficiency in Sport for Division I women athletes during a collegiate cross-country season: A case series. Front. Endocrinol. 2021;12:524762. doi: 10.3389/fendo.2021.524762. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Saenz C., Jordan A., Loriz L., Schill K., Colletto M., Rodriguez J. Low energy intake leads to body composition and performance decrements in a highly-trained, female athlete: The WANDER (Woman’s Activity and Nutrition during an Extensive Hiking Route) case study. J. Am. Nutr. Assoc. 2023;43:296–303. doi: 10.1080/27697061.2023.2282614. [DOI] [PubMed] [Google Scholar]
- 83.Wang M., Chee J., Tanaka M.J., Lee Y.H.D. Relative Energy Deficiency in Sport (REDs) and knee injuries: Current concepts for female athletes. J. Isakos. 2024;9:781–787. doi: 10.1016/j.jisako.2024.05.012. [DOI] [PubMed] [Google Scholar]
- 84.Saenz C., Sanders D.J., Brooks S.J., Bracken L., Jordan A., Stoner J., Vatne E., Wahler M., Brown A.F. The relationship between dance training volume, body composition, and habitual diet in female collegiate dancers: The Intercollegiate Artistic Athlete Research Assessment (TIAARA) study. Nutrients. 2024;16:3733. doi: 10.3390/nu16213733. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Chen Y.-L., Chang C.-C., Lin M.-P., Lin C.-C., Chen P.-Y., Juan C.-H. Chapter three-Association between physical activity, body composition, and cognitive performance among female office workers. Prog. Brain Res. 2024;286:67–87. doi: 10.1016/bs.pbr.2024.01.007. [DOI] [PubMed] [Google Scholar]
- 86.Cataldi D., Bennett J.P., Wong M.C., Quon B.K., Liu Y.E., Kelly N.N., Kelly T., Schoeller D.A., Heymsfield S.B., Shepherd J.A. Accuracy and precision of multiple body composition methods and associations with muscle strength in athletes of varying hydration: The Da Kine study. Clin. Nutr. 2024;43:284–294. doi: 10.1016/j.clnu.2023.11.040. [DOI] [PubMed] [Google Scholar]
- 87.Nickerson B.S., Esco M.R., Bishop P.A., Kliszczewicz B.M., Williford H.N., Park K.-S., Welborn B.A., Snarr R.L., Tolusso D.V. Effects of heat exposure on body water assessed using single-frequency bioelectrical impedance analysis and bioimpedance spectroscopy. Int. J. Exerc. Sci. 2017;10:1085–1093. doi: 10.70252/EWET6590. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88.Smith-Ryan A.E., Mock M.G., Ryan E.D., Gerstner G.R., Trexler E.T., Hirsch K.R. Validity and reliability of a 4-compartment body composition model using dual energy x-ray absorptiometry-derived blood volume. Clin. Nutr. 2017;36:825–830. doi: 10.1016/j.clnu.2016.05.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Nindl B.C. Physical training strategies for military women’s performance optimization in combat-centric occupations. J. Strength Cond. Res. 2015;29:S101–S106. doi: 10.1519/JSC.0000000000001089. [DOI] [PubMed] [Google Scholar]
- 90.Sterczala A.J., Krajewski K.T., Peterson P.A., Sekel N.M., Lovalekar M., Wardle S.L., O’Leary T.J., Greeves J.P., Flanagan S.D., Connaboy C., et al. Twelve weeks of concurrent resistance and interval training improves military occupational task performance in men and women. Eur. J. Sport. Sci. 2023;23:2411–2424. doi: 10.1080/17461391.2023.2239752. [DOI] [PubMed] [Google Scholar]
- 91.McNulty K.L., Taim B.C., Freemas J.A., Hassan A., Brantner C.L., Oleka C.T., Scott D., Howatson G., Moore I.S., Yung K.K., et al. Research across the female life cycle: Reframing the narrative for health and performance in athletic females and showcasing solutions to drive advancements in research and translation. Women Sport. Phys. Act. J. 2024;32:1–12. doi: 10.1123/wspaj.2024-0064. [DOI] [Google Scholar]
- 92.Gifford R.M., Reynolds R.M., Greeves J.P., Anderson R.A., Woods D.R. Reproductive dysfunction and associated pathology in women undergoing military training. J. R. Army Med. Corps. 2017;163:301–310. doi: 10.1136/jramc-2016-000727. [DOI] [PubMed] [Google Scholar]
- 93.Szivak T.K., Mala J., Kraemer W.J. Physical performance and integration strategies for women in combat arms. Strength Cond J. 2015;37:20–29. doi: 10.1519/SSC.0000000000000137. [DOI] [Google Scholar]
- 94.Kraemer W.J., Szivak T.K. Strength training for the warfighter. J. Strength Cond. Res. 2012;26:S107–S118. doi: 10.1519/JSC.0b013e31825d8263. [DOI] [PubMed] [Google Scholar]
- 95.Conkright W.R., O’Leary T.J., Wardle S.L., Greeves J.P., Beckner M.E., Nindl B.C. Sex differences in the physical performance, physiological, and psycho-cognitive responses to military operational stress. Eur. J. Sport. Sci. 2022;22:99–111. doi: 10.1080/17461391.2021.1916082. [DOI] [PubMed] [Google Scholar]
- 96.Giersch G.E.W., Charkoudian N., McClung H.L. The rise of the female warfighter: Physiology, performance, and future directions. Med. Sci. Sports Exerc. 2022;54:683–691. doi: 10.1249/MSS.0000000000002840. [DOI] [PubMed] [Google Scholar]
- 97.Bartman N.E., Hess H.W., Colburn D., Temple J., Hostler D. Heat strain in different hot environments hiking in wildland firefighting garments. Appl. Physiol. Nutr. Metab. 2024;50:1–14. doi: 10.1139/apnm-2024-0240. [DOI] [PubMed] [Google Scholar]
- 98.Berryman C.E., McClung H.L., Sepowitz J.J., Gaffney-Stomberg E., Ferrando A.A., McClung J.P., Pasiakos S.M. Testosterone status following short-term, severe energy deficit is associated with fat-free mass loss in U.S. Marines. Physiol. Rep. 2022;10:e15461. doi: 10.14814/phy2.15461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 99.Brown R.M., Tang X., Dreer L.E., Driver S., Pugh M.J., Martin A.M., McKenzie-Hartman T., Shea T., Silva M.A., Nakase-Richardson R. Change in body mass index within the first-year post-injury: A VA Traumatic Brain Injury (TBI) model systems study. Brain Inj. 2018;32:986–993. doi: 10.1080/02699052.2018.1468575. [DOI] [PubMed] [Google Scholar]
- 100.Bulmer S., Aisbett B., Drain J.R., Roberts S., Gastin P.B., Tait J., Main L.C. Sleep of recruits throughout basic military training and its relationships with stress, recovery, and fatigue. Int. Arch. Occup. Environ. Health. 2022;95:1331–1342. doi: 10.1007/s00420-022-01845-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 101.Chitra T., Karunanidhi S. The Impact of Resilience Training on Occupational Stress, Resilience, Job Satisfaction, and Psychological Well-being of Female Police Officers. J. Police Crim. Psychol. 2021;36:8–23. doi: 10.1007/s11896-018-9294-9. [DOI] [Google Scholar]
- 102.Choi B., Schnall P., Dobson M. Twenty-four-hour work shifts, increased job demands, and elevated blood pressure in professional firefighters. Int. Arch. Occup. Environ. Health. 2016;89:1111–1125. doi: 10.1007/s00420-016-1151-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 103.Christison K.S., Gurney S.C., Sol J.A., Williamson-Reisdorph C.M., Quindry T.S., Quindry J.C., Dumke C.L. Muscle Damage and Overreaching During Wildland Firefighter Critical Training. J. Occup. Environ. Med. 2021;63:350–356. doi: 10.1097/JOM.0000000000002149. [DOI] [PubMed] [Google Scholar]
- 104.Christison K.S., Sol J.A., Gurney S.C., Dumke C.L. Wildland Firefighter Critical Training Elicits Positive Adaptations to Markers of Cardiovascular and Metabolic Health. Wilderness Environ. Med. 2023;34:328–333. doi: 10.1016/j.wem.2023.04.003. [DOI] [PubMed] [Google Scholar]
- 105.Christodoulou A., Christophi C.A., Sotos-Prieto M., Moffatt S., Kales S.N. Eating Habits among US Firefighters and Association with Cardiometabolic Outcomes. Nutrients. 2022;14:2762. doi: 10.3390/nu14132762. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 106.Coker R.H., Murphy C.J., Johannsen M., Galvin G., Ruby B.C. Wildland Firefighting. J. Occup. Environ. Med. 2019;61:e91–e94. doi: 10.1097/JOM.0000000000001535. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 107.Coombs C.V., Wardle S.L., Shroff R., Eisenhauer A., Tang J.C.Y., Fraser W.D., Greeves J.P., O’Leary T.J. The effect of calcium supplementation on calcium and bone metabolism during load carriage in women: Protocol for a randomised controlled crossover trial. BMC Musculoskelet. Disord. 2023;24:1–8. doi: 10.1186/s12891-023-06600-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 108.Corbett J., Wright J., Tipton M.J. Sex differences in response to exercise heat stress in the context of the military environment. BMJ Mil. Health. 2020;169:94–101. doi: 10.1136/jramc-2019-001253. [DOI] [PubMed] [Google Scholar]
- 109.Di Nota P.M., Scott S.C., Huhta J.-M., Gustafsberg H., Andersen J.P. Physiological Responses to Organizational Stressors Among Police Managers. Appl. Psychophysiol. Biofeedback. 2024;49:85–102. doi: 10.1007/s10484-023-09613-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110.Diaz-Manzano M., Fuentes J.P., Fernandez-Lucas J., Aznar-Lain S., Clemente-Suárez V.J. Higher use of techniques studied and performance in melee combat produce a higher psychophysiological stress response. Stress Health. 2018;34:622–628. doi: 10.1002/smi.2829. [DOI] [PubMed] [Google Scholar]
- 111.Drain J.R., Groeller H., Burley S.D., Nindl B.C. Hormonal response patterns are differentially influenced by physical conditioning programs during basic military training. J. Sci. Med. Sport. 2017;20:S98–S103. doi: 10.1016/j.jsams.2017.08.020. [DOI] [PubMed] [Google Scholar]
- 112.Epstein Y., Yanovich R., Moran D.S., Heled Y. Physiological employment standards IV: Integration of women in combat units physiological and medical considerations. Eur. J. Appl. Physiol. 2013;113:2673–2690. doi: 10.1007/s00421-012-2558-7. [DOI] [PubMed] [Google Scholar]
- 113.Fagnant H.S., Armstrong N.J., Lutz L.J., Nakayama A.T., Guerriere K.I., Ruthazer R., Cole R.E., McClung J.P., Gaffney-Stomberg E., Karl J.P. Self-reported eating behaviors of military recruits are associated with body mass index at military accession and change during initial military training. Appetite. 2019;142:104348. doi: 10.1016/j.appet.2019.104348. [DOI] [PubMed] [Google Scholar]
- 114.Farina E.K., Taylor J.C., Means G.E., Murphy N.E., Pasiakos S.M., Lieberman H.R., McClung J.P. Effects of deployment on diet quality and nutritional status markers of elite U.S. Army special operations forces soldiers. Nutr. J. 2017;16:41. doi: 10.1186/s12937-017-0262-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 115.Farina E.K., Stein J.A., Thompson L.A., Knapik J.J., Pasiakos S.M., McClung J.P., Lieberman H.R. Longitudinal changes in psychological, physiological, and nutritional measures and predictors of success in Special Forces training. Physiol. Behav. 2025;291:114790. doi: 10.1016/j.physbeh.2024.114790. [DOI] [PubMed] [Google Scholar]
- 116.Flood A., Keegan R.J. Cognitive Resilience to Psychological Stress in Military Personnel. Front. Psychol. 2022;13:809003. doi: 10.3389/fpsyg.2022.809003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 117.Forse J.N., Koltun K.J., Bird M.B., Lovalekar M., Feigel E.D., Steele E.J., Martin B.J., Nindl B.C. Low psychological resilience and physical fitness predict attrition from US Marine Corps Officer Candidate School training. Mil. Psychol. 2024:1–10. doi: 10.1080/08995605.2024.2403826. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 118.Friedl K.E. Biomedical Research on Health and Performance of Military Women: Accomplishments of the Defense Women’s Health Research Program (DWHRP) J. Women’s Health. 2005;14:764–802. doi: 10.1089/jwh.2005.14.764. [DOI] [PubMed] [Google Scholar]
- 119.Gaffney-Stomberg E., Lutz L.J., Rood J.C., Cable S.J., Pasiakos S.M., Young A.J., McClung J.P. Calcium and vitamin D supplementation maintains parathyroid hormone and improves bone density during initial military training: A randomized, double-blind, placebo controlled trial. Bone. 2014;68:46–56. doi: 10.1016/j.bone.2014.08.002. [DOI] [PubMed] [Google Scholar]
- 120.Gnacinski S.L., Ebersole K.T., Cornell D.J., Mims J., Zamzow A., Meyer B.B. Firefighters’ cardiovascular health and fitness: An observation of adaptations that occur during firefighter training academies. Work. 2016;54:43–50. doi: 10.3233/WOR-162266. [DOI] [PubMed] [Google Scholar]
- 121.Gu J.K.M., Charles L.E., Burchfiel C.M., Fekedulegn D., Sarkisian K., Andrew M.E., Ma C., Violanti J.M. Long Work Hours and Adiposity Among Police Officers in a US Northeast City. J. Occup. Environ. Med. 2012;54:1374–1381. doi: 10.1097/JOM.0b013e31825f2bea. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 122.Harlow J., Blodgett K., Stedman J., Pojednic R. Dietary Supplementation on Physical Performance and Recovery in Active-Duty Military Personnel: A Systematic Review of Randomized and Quasi-Experimental Controlled Trials. Nutrients. 2024;16:2746. doi: 10.3390/nu16162746. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 123.Heblich F., Kähler W. Increased stress for firefighters due to wearing full-face masks? Zentralblatt Arb. 2020;70:1–7. [Google Scholar]
- 124.Hormeño-Holgado A.J., Perez-Martinez M.A., Clemente-Suárez V.J. Psychophysiological response of air mobile protection teams in an air accident manoeuvre. Physiol. Behav. 2019;199:79–83. doi: 10.1016/j.physbeh.2018.11.006. [DOI] [PubMed] [Google Scholar]
- 125.Hourani L.L., Williams T.V., Kress A.M. Stress, Mental Health, and Job Performance among Active Duty Military Personnel: Findings from the 2002 Department of Defense Health-Related Behaviors Survey. Mil. Med. 2006;171:849–856. doi: 10.7205/MILMED.171.9.849. [DOI] [PubMed] [Google Scholar]
- 126.Ibrahim F., Schumacher J., Schwandt L., Herzberg P.Y. The first shot counts the most: Tactical breathing as an intervention to increase marksmanship accuracy in student officers. Mil. Psychol. 2023;36:689–700. doi: 10.1080/08995605.2023.2258737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 127.Jayne J.M., Ayala R., Karl J.P., Deschamps B.A., McGraw S.M., O’Connor K., DiChiara A.J., Cole R.E. Body weight status, perceived stress, and emotional eating among US Army Soldiers: A mediator model. Eat. Behav. 2020;36:101367. doi: 10.1016/j.eatbeh.2020.101367. [DOI] [PubMed] [Google Scholar]
- 128.Jayne J.M., Blake C.E., Frongillo E.A., Liese A.D., Cai B., Nelson D.A., Kurina L.M., Funderburk L. Stressful Life Changes and Their Relationship to Nutrition-Related Health Outcomes Among US Army Soldiers. J. Prev. 2020;41:171–189. doi: 10.1007/s10935-020-00583-3. [DOI] [PubMed] [Google Scholar]
- 129.Korre M., Loh K., Eshleman E.J., Lessa F.S., Porto L.G., Christophi C.A., Kales S.N. Recruit fitness and police academy performance: A prospective validation study. Occup. Med. 2019;69:541–548. doi: 10.1093/occmed/kqz110. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 130.Kukić F., Koropanovski N., Jankovic R., Cvorovic A., Dawes J.J., Lockie G.R., Orr R.M., Dopsaj M. Association of Sex-Related Differences in Body Composition to Change of Direction Speed in Police Officers While Carrying Load. Int. J. Morphol. 2020;38:731–736. doi: 10.4067/S0717-95022020000300731. [DOI] [Google Scholar]
- 131.Kukić F., Streetman A., Heinrich K.M., Popović-Mančević M., Koropanovski N. Association between police officers’ stress and perceived health. Polic. A J. Policy Pract. 2023;17:paad058. doi: 10.1093/police/paad058. [DOI] [Google Scholar]
- 132.Lan F.-Y., Yiannakou I., Scheibler C., Hershey M.S., Cabrera J.L.R., Gaviola G.C., Fernandez-Montero A., Christophi C.A., Christiani D.C., Sotos-Prieto M., et al. The Effects of Fire Academy Training and Probationary Firefighter Status on Select Basic Health and Fitness Measurements. Med. Sci. Sports Exerc. 2021;53:740–748. doi: 10.1249/MSS.0000000000002533. [DOI] [PubMed] [Google Scholar]
- 133.Lieberman H.R., Thompson L.A., Caruso C.M., Niro P.J., Mahoney C.R., McClung J.P., Caron G.R. The catecholamine neurotransmitter precursor tyrosine increases anger during exposure to severe psychological stress. Psychopharmacology. 2015;232:943–951. doi: 10.1007/s00213-014-3727-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 134.Lin K.-H., Su F.-Y., Yang S.-N., Liu M.-W., Kao C.-C., Nagamine M., Lin G.-M. Body Mass Index and Association of Psychological Stress with Exercise Performance in Military Members: The Cardiorespiratory Fitness and Hospitalization Events in Armed Forces (CHIEF) Study. Endocr. Metab. Immune Disord.-Drug Targets. 2021;21:2213–2219. doi: 10.2174/1871530321666210427090550. [DOI] [PubMed] [Google Scholar]
- 135.McAllister M.J., Martaindale M.H., Rentería L.I. Active Shooter Training Drill Increases Blood and Salivary Markers of Stress. Int. J. Environ. Res. Public Health. 2020;17:5042. doi: 10.3390/ijerph17145042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 136.McAllister M.J., Martaindale M.H. Women demonstrate lower markers of stress and oxidative stress during active shooter training drill. Compr. Psychoneuroendocrinology. 2021;6:100046. doi: 10.1016/j.cpnec.2021.100046. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 137.McClung J.P., Karl J.P., Cable S.J., Williams K.W., Young A.J., Lieberman H.R. Longitudinal decrements in iron status during military training in female soldiers. Br. J. Nutr. 2009;102:605–609. doi: 10.1017/S0007114509220873. [DOI] [PubMed] [Google Scholar]
- 138.Morse J.L., Wooldridge J.S., Herbert M.S., Afari N. The Impact of COVID-19 on Health Behavior Engagement and Psychological and Physical Health Among Active Duty Military Enrolled in a Weight Management Intervention: An Exploratory Study. Mil. Med. 2024;189:e1840–e1845. doi: 10.1093/milmed/usae092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 139.Ojanen T., Häkkinen K., Hanhikoski J., Kyröläinen H. Effects of Task-Specific and Strength Training on Simulated Military Task Performance in Soldiers. Int. J. Environ. Res. Public Health. 2020;17:8000. doi: 10.3390/ijerph17218000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 140.Penatzer J.A., Miller J.V., Han A.A., Prince N., Boyd J.W. Salivary cytokines as a biomarker of social stress in a mock rescue mission. Brain Behav. Immun.-Health. 2020;4:100068. doi: 10.1016/j.bbih.2020.100068. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 141.Pineda Calderón C.F., Monteros Luzuriaga G.S., Yepez Herrera E.R., Guerron Varela E.R. Physical conditioning and its relationship with stress in the National Police of the Metropolitan District of Quito. Retos. 2023;48:505–510. doi: 10.47197/retos.v48.95201. [DOI] [Google Scholar]
- 142.Proessl F., Canino M.C., Beckner M.E., Conkright W.R., LaGoy A.D., Sinnott A.M., Eagle S.R., Martin B.J., Sterczala A.J., Roma P.G., et al. Use-dependent corticospinal excitability is associated with resilience and physical performance during simulated military operational stress. J. Appl. Physiol. 2022;132:187–198. doi: 10.1152/japplphysiol.00628.2021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 143.Ramey S.L., Downing N.R., Franke W.D., Perkhounkova Y., Alasagheirin M.H. Relationships Among Stress Measures, Risk Factors, and Inflammatory Biomarkers in Law Enforcement Officers. Biol. Res. Nurs. 2011;14:16–26. doi: 10.1177/1099800410396356. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 144.Rodas K.A., Dulla J.M., Moreno M.R., Bloodgood A.M., Thompson M.B., Orr R.M., Dawes J.J., Lockie R.G. The Effects of Traditional versus Ability-Based Physical Training on the Health and Fitness of Custody Assistant Recruits. Int. J. Exerc. Sci. 2022;15:1641–1660. doi: 10.70252/kprm9974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 145.Rosalky D.S., Hostler D., Webb H.E. Work duration does not affect cortisol output in experienced firefighters performing live burn drills. Appl. Ergon. 2017;58:583–591. doi: 10.1016/j.apergo.2016.04.008. [DOI] [PubMed] [Google Scholar]
- 146.Schilling R., Colledge F., Ludyga S., Pühse U., Brand S., Gerber M. Does Cardiorespiratory Fitness Moderate the Association between Occupational Stress, Cardiovascular Risk, and Mental Health in Police Officers? Int. J. Environ. Res. Public Health. 2019;16:2349. doi: 10.3390/ijerph16132349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 147.Schilling R., Herrmann C., Ludyga S., Colledge F., Brand S., Pühse U., Gerber M. Does Cardiorespiratory Fitness Buffer Stress Reactivity and Stress Recovery in Police Officers? A Real-Life Study. Front. Psychiatry. 2020;11:594. doi: 10.3389/fpsyt.2020.00594. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 148.Schilling R., Colledge F., Pühse U., Gerber M., Vandoni M. Stress-buffering effects of physical activity and cardiorespiratory fitness on metabolic syndrome: A prospective study in police officers. PLoS ONE. 2020;15:e0236526. doi: 10.1371/journal.pone.0236526. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 149.Scott J.M., Kazman J.B., Palmer J., McClung J.P., Gaffney-Stomberg E., Gasier H.G. Effects of vitamin D supplementation on salivary immune responses during Marine Corps basic training. Scand. J. Med. Sci. Sports. 2019;29:1322–1330. doi: 10.1111/sms.13467. [DOI] [PubMed] [Google Scholar]
- 150.Tait J.L., Drain J.R., Corrigan S.L., Drake J.M., Main L.C., Lomonaco T. Impact of military training stress on hormone response and recovery. PLoS ONE. 2022;17:e0265121. doi: 10.1371/journal.pone.0265121. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 151.Taylor M.K., Stone M., Laurent H.K., Rauh M.J., Granger D.A. Neuroprotective–neurotrophic effect of endogenous dehydroepiandrosterone sulfate during intense stress exposure. Steroids. 2014;87:54–58. doi: 10.1016/j.steroids.2014.05.011. [DOI] [PubMed] [Google Scholar]
- 152.Tegeler C.L., Gerdes L., Shaltout H.A., Cook J.F., Simpson S.L., Lee S.W., Tegeler C.H. Successful use of closed-loop allostatic neurotechnology for post-traumatic stress symptoms in military personnel: Self-reported and autonomic improvements. Mil. Med. Res. 2017;4:38. doi: 10.1186/s40779-017-0147-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 153.Tingestad H.C., Filion L.G., Martin J., Spivock M., Tang V., Haman F. Stress and immune mediators in the Canadian Armed Forces: Association between basal levels and military physical performance. J. Mil. Veterans Health. 2019;27:15–23. [Google Scholar]
- 154.Toczko M., Fyock-Martin M., McCrory S., Martin J. Effects of fitness on self-reported physical and mental quality of life in professional firefighters: An exploratory study. Work. 2023;76:1589–1596. doi: 10.3233/WOR-220673. [DOI] [PubMed] [Google Scholar]
- 155.Vicente-Rodríguez M., Fuentes-Garcia J.P., Clemente-Suárez V.J. Psychophysiological Stress Response in an Underwater Evacuation Training. Int. J. Environ. Res. Public Health. 2020;17:2307. doi: 10.3390/ijerph17072307. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 156.Visconti L.M., Palombo L.J., Givens A.C., Turcotte L.P., Kelly K.R. Stress Response to Winter Warfare Training: Potential Impact of Location. Mil. Med. 2024;189:196–204. doi: 10.1093/milmed/usae075. [DOI] [PubMed] [Google Scholar]
- 157.Watkins E.R., Hayes M., Watt P., Richardson A.J. Heat tolerance of Fire Service Instructors. J. Therm. Biol. 2019;82:1–9. doi: 10.1016/j.jtherbio.2019.03.005. [DOI] [PubMed] [Google Scholar]
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Data Availability Statement
All reported studies/experiments have been previously published with available data to support findings.



