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. 2025 Jun 7;11:65. doi: 10.1186/s40798-025-00883-0

Exploring the Effects of Lifestyle Disruptions on Physical Fitness in Children and Adolescents: a Systematic Scoping Review

Lou Dambel 1, Giovanna Del Sordo 1,2, Oussama Saidi 1, Pascale Duché 1,
PMCID: PMC12145346  PMID: 40481998

Abstract

Background

The objective of this scoping review was to systematically summarize the available literature investigating the impact of various lifestyle disruptions—including lockdowns, school vacations, and training cessation—on the physical fitness components of children and adolescents aged 4–18 years.

Methods

A search for relevant studies was conducted across PubMed and ScienceDirect databases (until May 2024). Study selection and data extraction were independently performed by two reviewers using the Cadima website. A graphical analysis was conducted to present the findings of the included studies based on the effects of each lifestyle disruption on physical fitness components, such as cardiorespiratory fitness, muscle strength, explosive strength or power, speed, agility, balance, and flexibility.

Results

A total of 223 records were initially identified, with 60 studies meeting the inclusion criteria for analysis. The studies assessed the impact of lockdowns (n = 8), school vacations (n = 16), and training cessation (n = 36) on various physical fitness components. The results indicated consistent declines in cardiorespiratory fitness, particularly among older adolescents, during these disruptions. In contrast, muscle strength and power remained relatively stable.

Conclusion

Lifestyle disruptions have a notable effect on physical fitness in children and adolescents. While different types of disruptions exert varying effects, all appear to significantly affect young populations. Further research is needed, particularly focusing on girls and incorporating better control of health-related behaviors during these periods. Understanding the long-term consequences and developing strategies to support and maintain youth fitness during such disruptions should be a priority.

Supplementary Information

The online version contains supplementary material available at 10.1186/s40798-025-00883-0.

Keywords: Physical Fitness, Lifestyle Disruption, Children, Adolescents, Health

Background

In response to the global health crisis triggered by the coronavirus disease outbreak, public policies faced an unprecedented challenge in implementing effective measures. These measures included movement restrictions, social distancing, and the closure of communal spaces such as schools, supermarkets, and sports clubs. However, given the lack of existing data, the decision to implement more severe measures (i.e., lockdowns) raised critical questions about their short- and long-term effect on health, especially among young people.

The abrupt cessation of school, sport and routine activities revealed the vulnerability of children and adolescents to sudden changes in their structured environment [1, 2]. Several studies have reported effects of COVID-19 induced disruptions on body mass [3], anxiety and mental health [4]. In addition, numerous studies have sought to assess the effect of these disruptions on children’s health behaviors, revealing significant changes in physical activity, sedentary behaviors, sleep, and diet [2, 5]. A scoping review conducted in 2021, including 150 studies, consistently reported declines in physical activity time, increases in screen time and total sedentary behavior, shifts to later bed and wake times, and increases in sleep duration in children and adolescents [6].

The pandemic induced significant disruptions in the daily lives of individuals, families, and communities [4]. Godber and Atkins [7] classify these disruptions into four main areas: (i) social lifestyle, encompassing changes or interruptions in evolving spaces and social interactions; (ii) learning, characterized by disruptions in educational processes, such as school closures; (iii) active lives, involving disturbances in patterns of physical activity, sedentary behaviors, and exercise; and (iv) livelihood, referring to interruptions or alterations in individuals’ means of earning income. According to this definition, other situations beyond the COVID-19 lockdown—such as school vacations, training cessation, imprisonment, or bed rest due to injury or illness—also qualify as disruptions. It is therefore essential to examine the effects of these various disruptive situations on the lifestyle and health behaviors (physical activity, sedentary behaviors, and sleep) of children and youth.

Lifestyle behaviors are associated with physical fitness [8, 9]. Physical fitness, defined as the physical ability to engage in physical activity, comprises a spectrum of components such as cardiorespiratory fitness, muscular strength and power, endurance, speed, flexibility, agility, and balance [10]. Surprisingly, despite being a key health predictor, the effects of lockdown on physical fitness have received limited attention [1114], with most of the studies addressing it being cross-sectional. Among these few, declines were reported in aerobic fitness and muscle strength during these restrictive periods [1517].

Students experience weeks of vacations annually, facing substantial disruptions during school closures. The “structured days hypothesis” [18] proposes a research framework suggesting that unstructured vacation days may lead to increased sedentary behavior and reduced physical activity levels. Similar to lockdown, recent research reports an increase in body mass [19, 20] over vacations, but studies exploring other components of physical fitness remain very scarce.

Training cessation, as defined by Bosquet et Mujika [21], refers to a temporary discontinuation or complete abandonment of a systematic program of physical conditioning, therefore also inducing disruptions [7]. In adults, the physiological adaptations induced by training and their loss through training cessation are both dependent on the duration of the cessation period and the baseline levels of the participants [22, 23]. In the literature on young populations, findings regarding the effects of training cessation are inconsistent. Studies indicate the maintenance of physical fitness [24] while others report a significant decrease in the assessed components [25].

Due to the absence or very small number of studies investigating physical fitness before and after a period of incarceration or bed rest in young population, the present analysis focuses on three primary lifestyle disruptions: lockdown, vacations, and training cessation. The aims of this scoping review are twofold: (1) to provide an overview of studies assessing physical fitness changes in young individuals during different lifestyle disruptions, (2) to identify potential moderators such as duration of the disruption and age and gender of the participants.

Methods

This systematic scoping review followed the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines for reporting in systematic reviews [26]. This review was not registered.

Inclusion Criteria

Studies that investigated the effects of lifestyle disruptions as defined by Godber et Akins [7] on physical fitness in children and adolescents were analyzed. The inclusion of studies followed the pre-determined population, intervention/exposure, comparator, outcome, and type of study (PICOT) criteria [27].

Population

Children and adolescents, girls, and boys (aged 4–18 years), without restrictions on clinical diagnosis, or on physical fitness levels. Infants and toddlers (aged 0–3 years) were excluded from the review due to their distinct movement behaviors and physical fitness characteristics [28, 29]. Studies were eligible for inclusion in the full-text review if they encompassed populations both within and outside the 4–18-year age range, if results were segmented by age. Additionally, studies with overlapping age ranges were considered, if most of the sample fell within the specified age range. In this review, we focused on the 4–18 years age group as our population of interest. However, some of the included studies also evaluated a broader age range [3032] but were still included due to their relevance to our research questions.

Intervention/exposure

Any articles that investigated physical fitness within the context of disruptive situations affecting young populations. “Lifestyle disruptions” represent situations that induced one of the disruptions identified by Godber et Atkins [7]. “Lockdown” is the temporary condition imposed by governmental authorities during the outbreak of COVID-19 in which people are required to stay in their homes and refrain from or limit activities [30]. This definition distinguishes a lockdown from the broader concept of the ‘COVID-19 pandemic’. “Vacations” refer to periods when schools and colleges are closed, such as summer vacations. This definition excludes individuals who participate in camps or school activities during vacation periods. “Training cessation” is a temporary discontinuation or complete abandonment of a systematic program of physical conditioning [21].

Comparator

Pre- and post-measures (before and after lockdown, vacations, and/or training cessation) in the same sample at different timepoints.

Outcomes

Any assessment of physical fitness components, including cardiorespiratory fitness, muscle strength and endurance, explosive power, speed, power-strength, flexibility, agility, and balance. These components had to be assessed using validated scales, questionnaires, or tests. Anthropometric measures were excluded from this review, as their effects had already been extensively investigated in previous studies addressing lockdowns, school vacations, and training cessation [3, 18, 31].

Type of Study

Only studies available in English and French were considered for inclusion. All pre-post longitudinal designs were considered for inclusion. Cross-sectional studies, reviews, meta-analyses, conference abstracts and protocols were excluded.

Search Strategy and Study Selection

The searches were conducted until May 2024. Papers published after June 1, 2024, were excluded from the final review. The searches were performed in the PubMed and ScienceDirect databases, and the reference lists of all selected articles were manually examined to identify any additional relevant studies. Due to the limited indexing of relevant articles, we complemented our search by exploring Google Scholar and general web sources to ensure comprehensive coverage of the literature and minimize potential biases (Fig. 1).

Fig. 1.

Fig. 1

PRISMA Flow chart of study literature search. (Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. doi: 10.1136/bmj.n71)

Study selection was facilitated using the Cadima website [32] as an evidence synthesis tool, with references lists imported for screening. Two reviewers (LD and GD) independently screened the titles and abstracts of the studies for eligibility and later retrieved full-text article. Two reviewers (LD and GD) then determined the eligibility of each study in accordance with inclusion and exclusion criteria. Any disagreements were discussed as a group (LD, GD, and PD) until consensus was reached. The full search strategy can be found in Appendix S1.

Data Extraction

Data extraction was carried out following the completion of screening. Two reviewers (LD and GD) extracted the included articles from the Cadima website and compiled them in an Excel file. Subsequently, another reviewer (PD) independently verified the accuracy of the extracted data. The following information was extracted from the included studies: (1) study details including authors, year of publication and country; (2) study design and aim; (3) population characteristics such as age, gender, and stage of maturation; (4) study procedure; (5) nature and duration of the disruption; types and characteristics of interventions/exposures; (6) outcome measures (physical fitness tests); and (6) results. The complete data extraction form can be found in Appendix S2.

Assessment of Studies’ Quality

Quality and risk of bias were assessed using three National Institute of Health tools for observational, before-after, and controlled intervention studies (NIH, 2021a, 2021b, 2021c). Each study received a global numerical quality score and an overall judgment (poor, fair, good). Scores below 55% were “poor,” 55–75% were “fair,” and above 75% were “good.” Two reviewers (LD and GD) independently assessed each study, resolving any disagreements through group discussion (LD, GD, PD). Full details are available in Appendices S5, S6 and S7.

Analysis Strategy

A meta-analysis of the selected studies was not conducted due to the high heterogeneity of outcome measures, interventions, study designs, and populations. Instead, a narrative analysis was conducted following the SWiM (Synthesis Without Meta-analysis) guidelines to report results [33]. Studies were categorized based on the type of lifestyle disruption and the physical fitness components affected. Given the varied terminologies in the literature, we recorded the specific tests used and the components they assessed, retaining the original authors’ classifications for unique or unfamiliar tests (Appendices S2, S3 and S4).

To enhance precision, outcomes were treated as individual data points, allowing multiple data points from a single study. When available, pre-, and post-values were converted to percentage changes; otherwise, only the effect direction (increase, decrease, or no change) was recorded. Then, the effects of disruptions were visualized by a traffic light graphical representation: red for “decrease,” yellow for “no change,” and green for “increase” in physical fitness. “Increase” indicates significant improvement, while “decrease” reflects a significant decline, such as a longer sprint time. “No change” indicates the lack of a statistically significant increase or decrease from pre- to post-disruption data, as reported by the authors. The effect of moderators (age, gender, duration) on physical fitness changes were graphically analyzed. Data points were included if they provided numerical values before and after disruptions, with sufficient data (> 50 points) required for inclusion, except for gender, where data on girls were insufficient. For these analyses, pre-post changes were expressed as percentages. Additionally, the baseline effect on physical fitness evolution was analyzed using data points from identical parameters measured by the same test (> 20 data points per parameter).

Results

Study Selection

The electronic search identified 223 potentially eligible reports: 185 from PubMed (n = 94) and ScienceDirect (n = 91). After removing duplicates, 124 records were screened at the title/abstract level, with 76 studies excluded. An additional 43 eligible records were found through website and reference list searches. Of the 89 full-text articles retrieved, 60 publications were considered relevant to evaluating the effect of lifestyle disruption on physical fitness. The study selection process is shown in Fig. 1.

Characteristics of the Included Studies

Eight studies analyzed the impact of lockdown on physical fitness [3441], while 16 studies explored the effects of school vacations [4257] and 36 studies investigated the effects of training cessation [24, 25, 5891], The duration of these disruptive situations ranged from 2 to 40 weeks. All studies that focused on the effect of school vacations specifically analyzed summer vacations. Sample sizes varied from 7 to 27,181 participants, with ages ranging from 7 to 19 years. The gender distribution was 38% boys (n = 23), 7% girls (n = 4), and 55% mixed (n = 32) (Appendices S2, S3, and S4).

Each study measured one or more physical fitness (PF) components, resulting in a total of 395 data points. Each data point represented an assessment of a unique PF component for one population group, pre- and post-disruption. For lockdowns (n = 88; 22%), PF components were measured in balanced proportions, with cardiorespiratory fitness (CRF) being the most frequently assessed component (n = 21; 24%). During vacations (n = 68; 17%), CRF was also the most studied component (n = 31; 46%). In studies investigating training cessation (n = 239; 61%), muscle strength (MS) was the most frequently analyzed component (n = 69; 29%) (Fig. 2, Panel A).

Fig. 2.

Fig. 2

Breakdown of data points. (Panel A) Breakdown by disruptive situation and by physical fitness component. (Panel B) Breakdown by disruptive situation, gender, and age range

Boys were the primary focus in both lockdown (n = 40; 51%) and training cessation (n = 150; 63%) studies. In school vacation studies, gender distribution was more balanced, with mixed-gender groups being the most frequently assessed (n = 30; 44%) (Fig. 2, Panel B).

Across the studies, 108 different tests were used to assess eight physical fitness components, with 32 methods specifically for muscle strength (Appendix S8).

Methodological Quality Assessments

The quality assessment results, summarized in Appendices S5, S6 and S7, utilized three different quality scales based on study design. Among 32 pre-post studies without control groups [25, 35, 40, 4245, 48, 5054, 57, 60, 61, 63, 69, 70, 7375, 78, 80, 81, 84, 87, 88, 9093], 87.5% were rated as good quality, with the main issue being unclear reporting [e.g., eligibility criteria, participant enrollment). Of the 22 controlled intervention studies [24, 47, 49, 56, 58, 59, 62, 6468, 71, 72, 76, 77, 79, 82, 83, 85, 86, 89], only 4 were rated as good quality, with 54.5% rated as fair and 6 as poor, primarily due to inadequate reporting (e.g., randomization, treatment allocation, blinding, power analysis, and statistical analysis). Six cross-sectional or cohort studies were assessed [3639, 41, 46], with 83% rated as good quality and one as poor, mainly due to missing power analyses, lack of blinding, and inadequate control of confounding variables.

Effect of Lockdown on Physical Fitness Components

Eight studies [3441] evaluating effects of lockdown on physical fitness in children provided 88 data points, with participants aged 6 to 22 years and sample sizes ranging from 31 to 27,681. Boys were the most assessed (n = 45; 51%), followed by girls (n = 22; 25%) and mixed-gender groups (n = 21; 24%). The duration of lockdown varied from 6 to 40 weeks (Fig. 3, Panel A).

Fig. 3.

Fig. 3

Traffic light analysis of pre- to post-disruption changes on physical fitness (PF) components. (Panel A) From pre- to post-lockdown. (Panel B) From pre- to post-vacations. (Panel C) From pre- to post- training cessation

*The bars represent the percentage of data points reporting significant increases (green), significant decreases (red), or no changes (yellow) in physical fitness components from pre- to post-disruption periods

**CRF: cardiorespiratory fitness, MS: muscle strength, EXP: explosive power, PS: power-strength, FLEX: flexibility, AG: agility, BAL: balance

Cardiorespiratory Fitness

Six studies [34, 3638, 40, 41] yielded 21 data points, making CRF the most frequently assessed component. Ten data points were obtained in males, 6 in females, and 5 in mixed gender groups. Most data points (n = 18; 86%) reported decreases in CRF, with reductions of up to 43%, primarily observed during lockdowns lasting 12 to 36 weeks. Two data points showed increases, and one reported no significant change. Among the 16 tests employed to assess CRF, he 20-m shuttle run test was the most used method (n = 6) (Appendix S8).

Muscle Strength

Seven data points from 2 studies [36, 40] studied muscle strength, with 3 data points in mixed gender groups and 2 in both males and females. The handgrip test was used in 6 out of 7 data points. No significant changes were observed in 4 data points (57%), while 2 data points (29%) reported improvements of up to 6%. One data point indicated a decrease after 24 weeks of lockdown.

Power-strength

Three studies [37, 38, 41] contributed 9 data points assessing power-strength. Four data points studied males and females separately, and one data point a mixed-gender group. Assessment methods included pull-ups to failure (n = 1), sit-ups within a minute (n = 5), and chin-ups within a minute (n = 3) (Appendix S8). No decreases were observed; 2 data points showed increases, and 7 data points (78%) reported no significant changes.

Explosive Strength or Power

Seven studies [3436, 3841] contributed 18 data points on explosive strength or power (EXP), with 61% of data points (n = 11) in males, 22% (n = 4) in females, and 17% (n = 3) in mixed-gender groups. Four different tests were used: the standing broad jump (n = 11), and the countermovement jump (n = 5) were the most frequently used (Appendix S8). A significant decline in EXP was observed in 9 data points (50%), with reductions of up to 30% during lockdowns lasting 6 to 40 weeks. Increases were reported in 3 data points, while 6 showed no significant changes.

Speed

Seven studies evaluated speed [34, 3641], yielding 17 data points (9 in males, 3 in females, 5 in mixed gender groups). The most frequently used tests were the 30-meters and 50-meters sprint tests, administered across 4 and 7 data points respectively, while repeated sprints (2 × 10 m and 4 × 10 m) were featured in 6 data points (Appendix S8). Decreases in speed performance were observed in 11 data points (65%), with reductions of up to 9.5% during lockdowns lasting 13 to 40 weeks. Five data points showed increases of up to 13%, and one data point indicated no significant change.

Motor Skills (agility, Balance, flexibility)

The influence of lockdown on agility [34, 37, 39] and flexibility [37, 38, 41] was investigated in 7 data points, and 3 studies each. Agility studies were most conducted on male participants (n = 5), while flexibility principally on mixed-gender groups (n = 3). Agility showed a predominant decline (n = 4; 57%), primarily reported by Alvurdu et al. [34]. Flexibility improved in 5 data points (72%), mostly in mixed-gender groups, while balance declined in 2 data points from Pombo et al. [39].

Effect of Vacations on Physical Fitness Components

Sixteen studies were included [4257], providing 68 data points. Participants were aged 6 to 17 years, with sample sizes ranging from 17 to 2,279. The gender distribution among data points was balanced: 19 in males, 19 in females, and 30 in mixed-gender groups. The duration of school vacations ranged from 3 to 24 weeks, and all studies focused on summer vacations (Fig. 3, Panel B).

Cardiorespiratory Fitness

All sixteen studies [4257] yielded 31 data points assessing CRF. Most data points (n = 19) were obtained from mixed-gender groups, while 6 were from males and 6 from females. The most frequently assessed outcomes were VO₂max (n = 12), number of laps of different distances (n = 15), and distance covered (n = 4) (Appendix S3). The PACER test was the most used method (n = 15) (Appendix S8). A decrease in CRF was observed in 8 data points (26%), with reductions ranging from 4 to 16% during vacations lasting 10 to 20 weeks. Increases were reported in 3 data points (10%), but the majority (n = 20; 64%) showed no significant changes.

Muscle Strength

A single study conducted by Aphamis et al. [55] assessed muscle strength using the handgrip test, yielding 4 distinct data points for analysis (2 in males and 2 in females) (Appendix S8). No significant changes in MS were observed across these data points.

Power-strength

Four studies [44, 48, 50, 53] investigated the effect of summer vacations on power-strength, providing 8 data points (2 in males, 2 in females, and 3 in mixed-gender groups). Three assessment methods were used: sit-ups within a 30-second, 40-second, or 1-minute period (n = 6), 40-second push-up test (n = 1), and push-up to failure test (n = 1) (Appendix S8). Most data points (n = 6; 75%) indicated no significant changes in power-strength, while 2 data points (25%) reported increases.

Explosive Strength or Power

Three studies [44, 53, 55]), contributed 7 data points assessing explosive power, with 3 in males, 3 in females, and 1 in mixed-gender groups. The standing broad jump (n = 5) and squat jump (n = 2) were the primary tests used (Appendix S8). Most data points (n = 5; 71%) showed no significant changes in EXP during vacations. One data point (14%) reported a decrease of 18% after 20 weeks of vacation, while another (14%) indicated an increase following 16 weeks of summer.

Speed

Three studies [44, 53, 55] provided 7 data points on speed, with 3 in males, 3 in females, and 1 in mixed-gender groups. Assessment methods included the 20-m sprint (n = 1), 30-m sprint (n = 2), and 10 × 5 m shuttle run (n = 4) (Appendix S8). Decreases in speed were observed in 3 data points (43%) after 20 weeks of vacation, while 4 data points (57%) showed no significant changes. No increases in speed were reported.

Motor Skills (agility, Balance, flexibility)

The impact of vacations on flexibility was investigated across 6 studies [44, 48, 50, 53, 55], yielding 9 data points. The sit-and-reach test (n = 8) and stand-and-reach test (n = 1) were used (Appendix S8). No changes were found in flexibility. Agility and balance showed significant declines in one study after 16 weeks of vacation [44].

Effect of Training Cessation on Physical Fitness

A total of 36 studies [24, 25, 5891] provided 239 data points to assess the impact of training cessation on physical fitness in children. Participants were aged 7 to 18 years, with sample sizes ranging from 7 to 256. Most assessments were conducted on males (n = 150), followed by mixed-gender groups (n = 62) and females (n = 27). The duration of training cessation varied from 2 to 24 weeks (Fig. 3, Panel C).

Cardiorespiratory Fitness

Thirteen studies [5961, 66, 69, 70, 74, 75, 78, 81, 8587] provided 23 data points on CRF (14 in males, 3 in females and 6 in mixed gender). The most frequently used tests were the 20-m shuttle run (n = 10) and the Yo-Yo Intermittent Recovery Test (n = 5) (Appendix S8). CRF decreased in 12 data points (52%), with reductions of up to 21% for periods of 3 to 24 weeks. No significant changes were observed in 9 data points, while increases were reported in 2 data points by D’souza and Avadhany [75].

Muscle Strength

Twenty-one studies [24, 59, 6264, 68, 69, 73, 75, 77, 79, 80, 82, 83, 8591] contributed 69 data points on MS, with 41 in males, 5 in females, and 23 in mixed-gender groups. A wide range of tests was used (n = 32), with medicine ball throwing (n = 18) and leg press (n = 6) being the most common (Appendix S8). No significant changes were found in 40 data points (58%), while 25 data points (36%) showed declines of up to 30% over training cessation periods of 4 to 16 weeks. Increases were reported in 4 data points (6%) in D’souza and Avadhany [75].

Power-strength

Eight studies [24, 66, 67, 69, 71, 75, 78, 87] provided 24 data points on power-strength, with 15 in mixed-gender groups, 6 in males, and 3 in females. The tests assessed either strength maintenance (n = 22) or speed maintenance (n = 2). Decreases in power strength, ranging from 3 to 64%, were observed in 12 data points (50%) over periods of 3 to 12 weeks. The remaining 12 data points (50%) showed no significant changes, and no increases were reported.

Explosive Strength or Power

Twenty-one studies [24, 25, 58, 60, 62, 64, 69, 7173, 7780, 8389, 91] provided 59 data points on explosive strength or power, with 41 in males, 9 in females, and 9 in mixed-gender groups. EXP was assessed through 12 different tests, with standing broad jump and countermovement jump being the most common (Appendix S8). Most data points (n = 36; 61%) showed no significant changes, while declines were reported in 21 data points (36%), with reductions of up to 30% for periods of 4 to 16 weeks. An increase was observed in one data point (3%) [84].

Speed

Twelve studies [25, 60, 64, 69, 74, 78, 80, 8386, 91] provided 34 data points on speed, predominantly in males (n = 32). Decreases in speed were observed in 18 data points (53%), with reductions of up to 11% during training cessation periods of 4 to 16 weeks. No significant changes were observed in 14 data points (41%), while increases were reported in 2 data points.

Motor Skills (agility, Balance, flexibility)

The effect of training cessation was most studied on balance (n = 11; 4 studies [60, 69, 71, 79]) and flexibility (n = 11; 5 studies [58, 65, 67, 69, 76]), then on agility (n = 8; 2 studies [60, 69]). Males were the most assessed gender group (n = 2; 50%). Data points indicated declines in agility (n = 6; 75%), balance (n = 4; 36%), and flexibility (n = 2; 18%). No increases were reported in any of the motor skills assessed.

Effect of Moderators

Cardiorespiratory fitness, muscle strength, explosive power and speed were the selected key parameters where sufficient data were available (> 50 data points).

Effect of Age

Regardless of the nature of the disruption, our analysis suggests that age influences CRF, MS, and speed differently. For CRF, the magnitude of decreases tends to escalate with age, indicating that older children and adolescents are more affected by disruptions. In contrast, younger children (before 12–13 years old) experience more pronounced declines in MS. Speed decreases are only observed in participants aged 13–14 years and older, suggesting different age sensitivities for these fitness components (Fig. 4).

Fig. 4.

Fig. 4

Pre- to post-disruption changes in physical fitness components across participants age (Panel A) In cardiorespiratory fitness. (Panel B) In muscle strength. (Panel C) In explosive power. (Panel D) In speed

Effect of Gender

The analysis did not reveal any consistent trends regarding the impact of disruptions based on gender. No clear patterns were identified across the different types of disruptions. A graphical analysis of the effect of gender is provided in Appendix S9.

Effect of Duration of the Disruption

The duration of the disruption did not seem to influence physical fitness outcomes. Decreases in physical fitness were similar regardless of whether the disruption was short (starting at 2 weeks) or extended (Fig. 5).

Fig. 5.

Fig. 5

Pre- to post-disruption changes in physical fitness components across duration of the disruptions (Panel A) In cardiorespiratory fitness. (Panel B) In muscle strength. (Panel C) In explosive power. (Panel D) In speed

Effect of Baseline VO2max

Due to the high variability in tests and parameters across studies, the analysis was restricted to CRF measured by VO2max or VO2peak assessment tests (23 data points) for comparability. The results indicated that higher initial VO2max levels are associated with more substantial declines in CRF following disruptions. These findings are illustrated in Fig. 6.

Fig. 6.

Fig. 6

VO2max baseline levels and pre- to post-disruption changes

Discussion

This systematic scoping review aimed to (1) map the effects of disruptive situations—lockdown, vacations, and training cessation—on the physical fitness components of children and adolescents, and (2) identify potentially moderators such as the duration of the disruption, age, gender, and baseline levels of the participants. A total of 60 longitudinal studies that explored the impact of disruptive situations on the physical fitness of young individuals were systematically identified. Most of the included studies focused on the effects of training cessation (n = 36) [24, 25, 5891], with a limited exploration of the impact of vacations (n = 16) [4257] and of lockdown (n = 8) [3441] on a young population.

The impact of various disruptions on cardiorespiratory fitness reveals distinct patterns (Fig. 3, Panel A). During lockdowns, a notable decline in CRF was observed. This is consistent with the study by Silva et al. (2022) [8] which noted that changes in aerobic capacity over time are influenced by physical activity and with findings from Paterson et al. (2021) [6] which indicate that lockdowns increased sedentary behavior and decreased physical activity levels. Therefore, restrictions due to lockdown on outdoor activities and organized sports reduced opportunities for maintaining physical activity levels, further influencing changes in aerobic capacity over time [8, 94]. This review found no data on lockdown effects on CRF in children, complicating age-related conclusions. However, it seems lockdown could induce decreases in CRF in both pre-adolescents and adolescents. Graphical analysis also did not reveal clear gender differences in response to lockdown, nor did it identify a correlation between lockdown duration and the magnitude of CRF decline.

In contrast, the impact of vacations on CRF varied among studies: 64% reported no significant changes, 26% observed decreases, and 10% noted increases. During vacations, children’s activities become unstructured without the school environment, leading to varied experiences and outcomes for everyone [18]. While some studies, like Fu et al. (2020) [46] or Watson et al. (2023) [95], reports declines in physical activity during vacations, others, such as Volmut et al. (2021) [96], find increases in outdoor activities and higher physical activity levels. These inconsistencies highlight a critical limitation in the literature: the inconsistent measurement of physical activity and sedentary during vacations. Furthermore, no significant effects of age, gender, or vacation duration on CRF were found, but the limited scope of studies limits broader generalizations.

CRF decreased in 52% of studies during training cessation, with 39% showing no significant changes, reflecting variability. Unlike lockdowns, training cessation may allow for other physical activities, explaining some of this inconsistency [7]. Furthermore, it primarily affects active youth, with higher baseline fitness levels, which is linked to greater CRF declines in adults [97]. For example, in young soccer players, those with higher VO2max values experienced declines exceeding 20% [25] (Fig. 6). Age also plays a role, as older adolescents tend to experience more significant CRF declines (Fig. 4). While VO2max increases during childhood, it tends to plateau after puberty [98], making adolescents more vulnerable to CRF loss when training stops. In contrast, younger children may see less decline due to maintaining spontaneous activity whereas sedentary behavior and inactivity peak during adolescence [99]. No significant gender differences were observed, and the length of detraining did not correlate with greater declines, consistent with findings that CRF drops as soon as training stops [71].

The effects on CRF are influenced by the specific context of disruptions. Lockdowns, with their broad restrictions on daily activities, led to significant CRF declines. Vacations showed varied effects, likely due to individual differences in unstructured activities and inconsistent measurement of movement behaviors. Training cessation mainly affected active individuals, with more pronounced declines linked to higher baseline fitness levels and older age.

The evolution of muscle strength and power-strength during disruptions remains relatively stable, with 57–100% and 50–78% of data points reporting no significant changes, respectively. MS and PS improve during childhood and adolescence because of natural growth (neuromuscular system) and maturation (muscular system) processes [100]. While environmental factors and physical activity influence these developments, they are largely driven by ongoing neuro-muscular growth, which mitigates the negative effects of disruptions [101]. Consequently, the stability of MS and PS is attenuated by the continuous growth and maturation, which attenuates the adverse effects of disruptive situations.

The most significant impacts on MS occur between ages 10 and 13, just before puberty (Fig. 4). In childhood, physical development is primarily neural, whereas adolescence involves both neural and hormonal changes [101]. Hormonal adaptations, which can occur even with low physical activity, lead to rapid gains in muscle mass and strength post-puberty [102], helping offset the effects of reduced activity or training cessation [101, 103]. No significant gender differences were observed, likely due to the limited data on girls (only 9 data points), making it difficult to draw conclusive gender comparisons. Duration also did not seem to influence the effects, as the magnitude of changes was consistent regardless of disruption length. Additionally, the wide variety of test methods (32 different tests) used to measure muscle strength complicates comparisons (Appendix S8). Future research should focus on assessing the impact of disruptions on muscle strength and power-strength in girls, using standardized testing methods.

The impacts of various disruptions on speed and explosive power reveal questioning patterns. Both qualities rely heavily on the neuromuscular system [104]. However, their responses to disruptions vary in magnitude depending on the nature of the disruptive situation. Explosive strength or power power seems more resilient than speed, particularly during lockdowns, where 65% of data points reported decreases in speed and 50% in explosivity. The severe impact of lockdown is likely due to the sudden cessation of school and structured physical activity, along with limited opportunities for high-intensity activities [6]. However, responses were more balanced over the other two disruptive situations, as declines in speed were less pronounced in vacations and training cessation (43% and 53%, respectively) and a major portion of data points reported no significant changes in explosive strength or power (72% and 61%, respectively). This may be due to the less restrictive nature of these disruptions, which allowed for the maintenance of unstructured physical activity and active situations [96].

Speed primarily relies on the neuromuscular system, which requires consistent, high-intensity training to maintain the coordination and efficiency of nerve impulses and muscle contractions [105]. Without regular practice, these neuromuscular connections weaken, leading to a more pronounced decline in speed [106]. In contrast, explosivity depends more on the muscular system’s strength and power. While neuromuscular coordination is also important, the primary factor is the muscle’s ability to generate force quickly. Muscle power can be more resilient to periods of detraining, as it does not degrade as rapidly as neuromuscular efficiency [89].

Age seems to moderate speed’s response to disruptions, with most declines occurring after 12–13 years, likely due to interactions between growth, maturation, and training [107]. Adolescents, especially those post-puberty and with higher training levels, seem more susceptible to declines in fitness when training is disrupted. However, the data primarily focus on adolescents, limiting conclusions. No age effects were observed for explosive strength or power, and no gender or duration effects were noted across the disruptions.

The following discussion aims to explain the observed effects of disruptions on flexibility, agility, and balance though conclusions are cautious due to the limited data available. Disruptions seem to have minimal impact on flexibility, with 89% of data points during vacations and 82% during training cessation showing maintenance. This stability is likely due to the strong genetic influence on flexibility, as noted by Massidda et al. [108] Interestingly, 72% of studies during COVID-19 lockdowns reported improvements in flexibility, particularly in China, where authorities promoted indoor physical exercises to maintain fitness, as noted by Li and Cheong [37]. As described a decade ago [101], agility remains under-researched in youth, with only 15 data points available. Most of these indicate decreases in agility across all disruptions: 67% during lockdown, 100% during vacations, and 75% during training cessation. Evidence from training studies suggests that agility is trainable in youth, and is therefore sensitive to the cessation of occasions to train this component, which likely explains these decreases [109]. Balance, less influenced by genetics and more by person-specific environmental factors [105], showed decreases in many data points. This trainable aspect of the component could explain why many data points reported decreases in balance.

Strengths and Limitations

Key strengths of this scoping review include a systematic search strategy and quality assessment. The review uniquely groups three disruptive scenarios—lockdowns, vacations, and training cessation—to examine their effects on physical fitness, marking to our knowledge the first such analysis.

However, the wide variability in testing methods across studies complicates comparisons, thereby limiting the strength of the conclusions. The small number of studies, especially those involving girls, further challenges the ability to draw definitive conclusions. Additionally, the lack of control for key health behaviors like physical activity, sedentary behaviors, and sleep during disruptions weakens the level of evidence by limiting our ability to fully assess the impact of these situations.

Conclusion

Disruptive situations like lockdowns, vacations, and training cessations have impacted the physical fitness of children and adolescents, with effects varying by disruption type. Cardiorespiratory fitness generally declined, particularly among older adolescents, highlighting the need for regular physical activity to maintain heart and lung health. In contrast, muscular fitness—encompassing strength, power, speed, and explosive strength or power—remained relatively stable, likely due to ongoing growth and maturation. Given the heightened sensitivity of older adolescents to these disruptions, physical activity guidelines should focus on this group.

The review reveals a need for more longitudinal studies to better understand the long-term impacts of disruptions on physical fitness. It also underscores the importance of addressing the gender gap by prioritizing research on girls. Assessing baseline fitness levels and controlling movement behaviors during disruptions are crucial for enhancing the accuracy and applicability of findings on how these situations affect physical fitness in youth.

Electronic Supplementary Material

Below is the link to the electronic supplementary material.

40798_2025_883_MOESM1_ESM.docx (140.7KB, docx)

Supplementary Material 1: Appendix S1 - Search strategy for each database.

40798_2025_883_MOESM2_ESM.xlsx (10.9KB, xlsx)

Supplementary Material 2: Appendix S2 - Data extraction of studies on lockdown

40798_2025_883_MOESM3_ESM.xlsx (85KB, xlsx)

Supplementary Material 3: Appendix S3 - Data extraction of studies on school vacations

40798_2025_883_MOESM4_ESM.xlsx (46.1KB, xlsx)

Supplementary Material 4: Appendix S4 - Data extraction of studies on training cessation

40798_2025_883_MOESM5_ESM.xlsx (92.9KB, xlsx)

Supplementary Material 5: Appendix S5 - Quality assessment of pre-post studies with no control groups

40798_2025_883_MOESM6_ESM.xlsx (14KB, xlsx)

Supplementary Material 6: Appendix S6 - Quality assessment of controlled intervention studies

40798_2025_883_MOESM7_ESM.xlsx (13.5KB, xlsx)

Supplementary Material 7: Appendix S7 - Quality assessment of cross-sectional and cohort studies

40798_2025_883_MOESM8_ESM.xlsx (13.9KB, xlsx)

Supplementary Material 8: Appendix S8 - Summary of tests employed in studies and their frequency of use

40798_2025_883_MOESM9_ESM.xlsx (15.2KB, xlsx)

Supplementary Material 9: Appendix S9 - Effect of disruptions in boys, girls and mixed groups

Supplementary Material 10 (238.4KB, jpg)

Acknowledgements

Not applicable.

Abbreviations

CRF

Cardio respiratory fitness

EXP

Explosive strength or power

MS

Muscle strength

PS

Power-strength

Author Contributions

LD was responsible for developing the search strategies, conducting the screening, performing full-text reviews, extracting data, analyzing results, and drafting the initial manuscript. GD participated in the screening and full-text reviews, conducted quality assessments, and assisted with data extraction. PD formulated the research question, supervised the search and screening processes, and provided editorial guidance on the manuscript. OS contributed to drafting the manuscript and provided critical revisions.

All authors have read and approved the final version of the manuscript and agree with the order of presentation of the authors.

Funding

No funding was received for the review.

Data Availability

The data used to support the findings of this study are included within the article and the supplementary information file.

Declarations

Ethics Approval and Consent to Participate

Not applicable.

Consent for Publication

Not applicable.

Competing Interests

The authors have no competing financial or non-financial interests that are related to this manuscript.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Giuntella O, Hyde K, Saccardo S, Sadoff S. Lifestyle and mental health disruptions during COVID-19. Proc Natl Acad Sci. 2021;118:e2016632118. 10.1073/pnas.2016632118. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Panda PK, Gupta J, Chowdhury SR, Kumar R, Meena AK, Madaan P, et al. Psychological and behavioral impact of lockdown and quarantine measures for COVID-19 pandemic on children, adolescents and caregivers: A systematic review and Meta-Analysis. J Trop Pediatr. 2020;fmaa122. 10.1073/pnas.2016632118. [DOI] [PMC free article] [PubMed]
  • 3.Basterfield L, Burn NL, Galna B, Batten H, Goffe L, Karoblyte G, et al. Changes in children’s physical fitness, BMI and health-related quality of life after the first 2020 COVID-19 lockdown in England: A longitudinal study. J Sports Sci. 2022;40:1088–96. 10.1080/02640414.2022.2047504. [DOI] [PubMed] [Google Scholar]
  • 4.Curtis MG, Floresca YB, Davoudpour S, Xu J, Phillips G. Patterns of COVID-19 related lifestyle disruptions and their associations with mental health outcomes among youth and young adults. J Mood Anxiety Disord. 2023;4:100029. 10.1016/j.xjmad.2023.100029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Richards AB, Sheldrick MP, Swindell N, Barker HG, Hudson J, Stratton G. Qualitative changes in children’s physical activity and sedentary behaviours throughout the COVID-19 pandemic: the homespace project. PLoS ONE. 2023;18:e0280653. 10.1371/journal.pone.0280653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Paterson DC, Ramage K, Moore SA, Riazi N, Tremblay MS, Faulkner G. Exploring the impact of COVID-19 on the movement behaviors of children and youth: A scoping review of evidence after the first year. J Sport Health Sci. 2021;10:675–89. 10.1016/j.jshs.2021.07.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Godber KA, Atkins DR. Sport and recreation undergraduate students’ perspectives on disruption of lifestyle, active lives, learning, and livelihood during pandemic times. COVID. 2023;3:1356–79. 10.3390/covid3090094. [Google Scholar]
  • 8.Silva DAS, De Andrade Gonçalves EC, Coelho EF, Cerqueira MS, Werneck FZ. Cardiorespiratory fitness and physical activity among children and adolescents: 3-Year longitudinal study in Brazil. Int J Environ Res Public Health. 2022;19:11431. 10.3390/ijerph191811431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Fonseca APLM, Azevedo CVMD, Santos RMR. Sleep and health-related physical fitness in children and adolescents: a systematic review. Sleep Sci. 2021;14:357–65. 10.5935/1984-0063.20200125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Ruiz JR, Castro-Piñero J, Artero EG, Ortega FB, Sjöström M, Suni J, et al. Predictive validity of health-related fitness in youth: a systematic review. Br J Sports Med. 2009;43:909–23. 10.1136/bjsm.2008.056499. [DOI] [PubMed] [Google Scholar]
  • 11.Santos R, Mota J, Okely AD, Pratt M, Moreira C, Coelho-e-Silva MJ, et al. The independent associations of sedentary behaviour and physical activity on cardiorespiratory fitness. Br J Sports Med. 2014;48:1508–12. 10.1136/bjsports-2012-091610. [DOI] [PubMed] [Google Scholar]
  • 12.Sagelv EH, Hopstock LA, Morseth B, Hansen BH, Steene-Johannessen J, Johansson J, et al. Device-measured physical activity, sedentary time, and risk of all-cause mortality: an individual participant data analysis of four prospective cohort studies. Br J Sports Med. 2023;57:1457–63. 10.1136/bjsports-2022-106568. [DOI] [PubMed] [Google Scholar]
  • 13.Marques A, Santos R, Ekelund U, Sardinha LB. Association between physical activity, sedentary time, and healthy fitness in youth. Med Sci Sports Exerc. 2015;47:575–80. 10.1249/MSS.0000000000000426. [DOI] [PubMed] [Google Scholar]
  • 14.Ortega FB, Ruiz JR, Castillo MJ, Sjöström M. Physical fitness in childhood and adolescence: a powerful marker of health. Int J Obes. 2008;32:1–11. 10.1038/sj.ijo.0803774. [DOI] [PubMed] [Google Scholar]
  • 15.Béghin L, Thivel D, Baudelet J-B, Deschamps T, Ovigneur H, Vanhelst J. Change in physical fitness due to the COVID-19 pandemic lockdown in French adolescents: a comparison between two independent large samples from diagnoform battery. Eur J Pediatr. 2022;181:3955–63. 10.1007/s00431-022-04610-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Chambonniere C, Fearnbach SN, Fearnbach N, Léna P, Genin P, Fillon A, et al. Adverse collateral effects of COVID-19 public health restrictions on physical fitness and cognitive performance in primary school children. Int J Environ Res Public Health. 2021;18:11099. 10.3390/ijerph182111099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Chen S, Wang B, Imagbe S, Gu X, Androzzi J, Liu Y, et al. Adolescents’ behaviors, fitness, and knowledge related to active living before and during the COVID-19 pandemic: A repeated Cross-Sectional analysis. Int J Environ Res Public Health. 2022;19:2560. 10.3390/ijerph19052560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Brazendale K, Beets MW, Weaver RG, Pate RR, Turner-McGrievy GM, Kaczynski AT, et al. Understanding differences between summer vs. school obesogenic behaviors of children: the structured days hypothesis. Int J Behav Nutr Phys Act. 2017;14:100. 10.1186/s12966-017-0555-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Baranowski T, O’Connor TM, Johnston CA, Hughes SO, Moreno JP, Chen T-A, et al. School year versus summer differences in child weight gain: A narrative review. Child Obes. 2014;10:18–24. 10.1089/chi.2013.0116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.von Hippel PT, Workman J. From kindergarten through second grade, U.S. Children’s obesity prevalence grows only during summer vacations. Obesity. 2016;24:2296–300. 10.1002/oby.21613. [DOI] [PubMed] [Google Scholar]
  • 21.Bosquet L, Mujika I, Detraining. Endur Train Sci Pract Pp 100–6, n.d.
  • 22.Mujika I, Padilla S, Detraining. Loss of training-Induced physiological and performance adaptations. Part I: short term insufficient training stimulus. Sports Med. 2000;30:79–87. 10.2165/00007256-200030020-00002. [DOI] [PubMed] [Google Scholar]
  • 23.Mujika I, Padilla S, Detraining. Loss of training-Induced physiological and performance adaptations. Part II: long term insufficient training stimulus. Sports Med. 2000;30:145–54. 10.2165/00007256-200030030-00001. [DOI] [PubMed] [Google Scholar]
  • 24.Vassilis S, Yiannis M, Athanasios M, Dimitrios M, Ioannis G, Thomas M. Effect of a 4-week detraining period followed by a 4-week strength program on isokinetic strength in elite youth soccer players. J Exerc Rehabil. 2019;15:67–73. 10.12965/jer.1836538.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Melchiorri G, Viero V, Lentini D, Annino G, Tancredi V, Triossi T. Effects of long-term detraining on muscle performance in young soccer players. J Sports Med Phys Fit. 2022. 10.23736/S0022-4707.22.13948-4. [DOI] [PubMed] [Google Scholar]
  • 26.Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;n71. 10.1136/bmj.n71. [DOI] [PMC free article] [PubMed]
  • 27.Schardt C, Adams MB, Owens T, Keitz S, Fontelo P. Utilization of the PICO framework to improve searching pubmed for clinical questions. BMC Med Inf Decis Mak. 2007;7:16. 10.1186/1472-6947-7-16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Timmons BW, LeBlanc AG, Carson V, Connor Gorber S, Dillman C, Janssen I, et al. Systematic review of physical activity and health in the early years (aged 0–4 years). Appl Physiol Nutr Metab. 2012;37:773–92. 10.1139/h2012-070. [DOI] [PubMed] [Google Scholar]
  • 29.Zhao R, Li X, Wang J, Zhang L, Gao Z. Evaluation of physical fitness and health of young children aged between 3 and 6 based on cluster and factor analyses. BMC Public Health. 2024;24:420. 10.1186/s12889-024-17660-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Lu Z, Mao C, Tan Y, Zhang X, Li Z, Zhang L, et al. Trends in physical fitness and nutritional status among School-Aged children and adolescents during the COVID-19 pandemic in Shaanxi, China—A Cross-Sectional study. Nutrients. 2022;14:3016. 10.3390/nu14153016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Pereira LA, Freitas TT, Pivetti B, Alcaraz PE, Jeffreys I, Loturco I. Short-Term detraining does not impair strength, speed, and power performance in elite young soccer players. Sports. 2020;8:141. 10.3390/sports8110141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Rodríguez-Fernández A, Sánchez-Sánchez J, Ramirez-Campillo R, Rodríguez-Marroyo JA, Villa Vicente JG, Nakamura FY. Effects of short-term in-season break detraining on repeated-sprint ability and intermittent endurance according to initial performance of soccer player. PLoS ONE. 2018;13:e0201111. 10.1371/journal.pone.0201111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Woc-Colburn L, Godinez D. Lockdown as a public health measure. COVID-19 Pandemic, Elsevier; 2022, pp. 133–6. 10.1016/B978-0-323-82860-4.00013-6
  • 34.Olds T, Dumuid D, Eglitis E, Golley R, Fraysse F, Miatke A, et al. Changes in fitness and fatness in Australian schoolchildren during the summer holidays: fitness lost, fatness regained? A cohort study. BMC Public Health. 2023;23:2094. 10.1186/s12889-023-17009-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Kohl C, McIntosh EJ, Unger S, Haddaway NR, Kecke S, Schiemann J, et al. Online tools supporting the conduct and reporting of systematic reviews and systematic maps: a case study on CADIMA and review of existing tools. Environ Evid. 2018;7:8. 10.1186/s13750-018-0115-5. [Google Scholar]
  • 36.Campbell M, McKenzie JE, Sowden A, Katikireddi SV, Brennan SE, Ellis S, et al. Synthesis without meta-analysis (SWiM) in systematic reviews: reporting guideline. BMJ. 2020;l6890. 10.1136/bmj.l6890. [DOI] [PMC free article] [PubMed]
  • 37.Alvurdu S, Baykal C, Akyildiz Z, Şenel Ö, Silva AF, Conte D, et al. Impact of prolonged absence of organized training on body composition, neuromuscular performance, and aerobic capacity: A study in youth male soccer players exposed to COVID-19 lockdown. Int J Environ Res Public Health. 2022;19:1148. 10.3390/ijerph19031148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Dauty M, Grondin J, Daley P, Louguet B, Menu P, Fouasson-Chailloux A. Consequences of the SARS-CoV-2 infection on anaerobic performances in young elite soccer players. Int J Environ Res Public Health. 2022;19. 10.3390/ijerph19116418. [DOI] [PMC free article] [PubMed]
  • 39.Jarnig G, Kerbl R, van Poppel M. The impact of COVID-19-Related mitigation measures on the health and fitness status of primary school children in Austria: A longitudinal study with data from 708 children measured before and during the ongoing COVID-19 pandemic. Sports. 2022;10:43. 10.3390/sports10030043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Li H, Cheong JPG. The impact of the COVID-19 pandemic on the physical fitness of primary school students in China based on the Bronfenbrenner ecological theory. Front Psychol. 2022;13:896046. 10.3389/fpsyg.2022.896046. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Pombo A, Luz C, de Sá C, Rodrigues LP, Cordovil R. Effects of the COVID-19 lockdown on Portuguese children’s motor competence. Children. 2021;8:199. 10.3390/children8030199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Ramos Álvarez O, Arufe Giráldez V, Cantarero Prieto D, Ibáñez García A. Changes in physical fitness, dietary habits and family habits for Spanish children during SARS-CoV-2 lockdown. Int J Environ Res Public Health. 2021;18:13293. 10.3390/ijerph182413293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Zhou T, Zhai X, Wu N, Koriyama S, Wang D, Jin Y, et al. Changes in physical fitness during COVID-19 pandemic lockdown among adolescents: A longitudinal study. Healthcare. 2022;10:351. 10.3390/healthcare10020351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Butterfield SA, Lehnhard RA, AEROBIC PERFORMANCE BY CHILDREN IN. GRADES 4 T O 8: A REPEATED-bIEASURES STUDY n.d.:16. [DOI] [PubMed]
  • 45.Rodriguez AX, Olvera N, Leung P, O’Connor DP, Smith DW. Association between the summer season and body fatness and aerobic fitness among Hispanic children. J Sch Health. 2014;84:233–8. 10.1111/josh.12141. [DOI] [PubMed] [Google Scholar]
  • 46.Drenowatz C, Ferrari G, Greier K. Changes in physical fitness during summer months and the school year in Austrian elementary school Children—A 4-Year longitudinal study. Int J Environ Res Public Health. 2021;18:6920. 10.3390/ijerph18136920. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Brusseau T, Burns R. Children’s weight gain and cardiovascular fitness loss over the summer. Int J Environ Res Public Health. 2018;15:2770. 10.3390/ijerph15122770. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Fu Y, Brusseau TA, Hannon JC, Burns RD. Effect of a 12-Week summer break on school day physical activity and Health-Related fitness in Low-Income children from CSPAP schools. J Environ Public Health. 2017;2017:1–7. 10.1155/2017/9760817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Takacs H, Martos E, Kovacs VA. Effects of a practice-focused nutrition intervention in Hungarian adolescents. Ann Ist Super Sanita. 2020;56:99–106. 10.4415/ANN_20_01_14. [DOI] [PubMed] [Google Scholar]
  • 50.Park K-S, Lee M-G. Effects of summer school participation and psychosocial outcomes on changes in body composition and physical fitness during summer break. J Exerc Nutr Biochem. 2015;19:81–90. 10.5717/jenb.2015.15052005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Meucci M, Cook C, Curry CD, Guidetti L, Baldari C, Collier SR. Effects of supervised exercise program on metabolic function in overweight adolescents. World J Pediatr WJP. 2013;9:307–11. 10.1007/s12519-013-0440-2. [DOI] [PubMed] [Google Scholar]
  • 52.Vieira BA, Leonel LDS, Katcipis LFG, Silveira JD, Dallegrave EJ, Delevatti RS. Effects of the vacation period on the health-related physical fitness of schoolchildren. Rev Bras Educ Física E Esporte. 2022;36:e36182831. 10.11606/issn.1981-4690.2022e36182831. [Google Scholar]
  • 53.Weaver RG, Hunt E, Armstrong B, Beets MW, Brazendale K, Turner-McGrievy G, et al. Impact of a year‐round school calendar on children’s BMI and fitness: final outcomes from a natural experiment. Pediatr Obes. 2021;16. 10.1111/ijpo.12789. [DOI] [PMC free article] [PubMed]
  • 54.Brusseau TA, Burns RD, Fu Y, Weaver RG. Impact of Year-Round and traditional school schedules on summer weight gain and fitness loss. Child Obes Print. 2019;15:541–7. 10.1089/chi.2019.0070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Christodoulos AD, Flouris AD, Tokmakidis SP. Obesity and physical fitness of pre-adolescent children during the academic year and the summer period: effects of organized physical activity. J Child Health Care. 2006;10:199–212. 10.1177/1367493506066481. [DOI] [PubMed] [Google Scholar]
  • 56.Mann S, Wade M, Jones M, Sandercock G, Beedie C, Steele J. One year surveillance of body mass index and cardiorespiratory fitness in primary school children in North West England and the impact of school deprivation level. SportRxiv. 2018. 10.31236/osf.io/jd9pv. [DOI] [PubMed] [Google Scholar]
  • 57.Aphamis G, Ioannou Y, Giannaki CD. Physical fitness and obesity levels during an academic year followed by summer holidays: an issue of insufficient time for physical activity. Int J Adolesc Med Health. 2019;31:20160137. 10.1515/ijamh-2016-0137. [DOI] [PubMed] [Google Scholar]
  • 58.Carrel AL, Clark RR, Peterson S, Eickhoff J, Allen DB. School-Based fitness changes are lost during the summer vacation. ARCH PEDIATR ADOLESC MED. 2007;161:4. [DOI] [PubMed] [Google Scholar]
  • 59.Peralta M, Marques A, Ferrari G, Martins J, López-Flores M, Minderico C, et al. The effect of school year and summer break in health-related cardiorespiratory fitness: A 2-year longitudinal analysis. J Sports Sci. 2022;40:1175–82. 10.1080/02640414.2022.2057004. [DOI] [PubMed] [Google Scholar]
  • 60.Donti O, Papia K, Toubekis A, Donti A, Sands WA, Bogdanis GC. Acute and long-term effects of two different static stretching training protocols on range of motion and vertical jump in preadolescent athletes. Biol Sport. 2021;38:579–86. 10.5114/biolsport.2021.101127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Santana-Sosa E, Gonzalez-Saiz L, Groeneveld IF, Villa-Asensi JR, Barrio Gómez de Aguero MI, Fleck SJ, et al. Benefits of combining inspiratory muscle with whole muscle training in children with cystic fibrosis: a randomised controlled trial. Br J Sports Med. 2014;48:1513–7. 10.1136/bjsports-2012-091892. [DOI] [PubMed] [Google Scholar]
  • 62.Clemente FM, Soylu Y, Arslan E, Kilit B, Garrett J, van den Hoek D, et al. Can high-intensity interval training and small-sided games be effective for improving physical fitness after detraining? A parallel study design in youth male soccer players. PeerJ. 2022;10:e13514. 10.7717/peerj.13514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Melchiorri G, Ronconi M, Triossi T, Viero V, De Sanctis D, Tancredi V, Salvati A, Padua E, Alvero Cruz JR. Detraining in young soccer players. J Sports Med Phys Fit 2014. [PubMed]
  • 64.Garrido N, Marinho DA, Reis VM, van den Tillaar R, Costa AM, Silva AJ, et al. Does combined dry land strength and aerobic training inhibit performance of young competitive swimmers? J Sports Sci Med. 2010;9:300–10. [PMC free article] [PubMed] [Google Scholar]
  • 65.Fathi A, Hammami R, Moran J, Borji R, Sahli S, Rebai H. Effect of a 16-Week combined strength and plyometric training program followed by a detraining period on athletic performance in pubertal volleyball players. J Strength Cond Res. 2019;33:2117–27. 10.1519/JSC.0000000000002461. [DOI] [PubMed] [Google Scholar]
  • 66.Katsanis et al. Effect of a school-based resistance training program using a suspension training system on strength parameters in adolescents. J Phys Educ Sport n.d.;21.
  • 67.Mayorga-Vega D, Merino-Marban R, Sánchez-Rivas E. Effect of a short-term static stretching training program followed by five weeks of detraining on hamstring extensibility in children aged 9–10 years n.d.
  • 68.Fazelifar S, Ebrahim K, Sarkisian V, EFFECT OF CONCURRENT TRAINING, AND DETRAINING ON ANTI-INFLAMMATORY BIOMARKER AND PHYSICAL FITNESS LEVELS IN OBESE CHILDREN. Rev Bras Med Esporte 2013;19.
  • 69.González-Gálvez N, Vaquero-Cristóbal R, Marcos-Pardo PJ. Effect of pilates method on muscular trunk endurance and hamstring extensibility in adolescents during twelve weeks training and detraining. J Bodyw Mov Ther. 2020;24:11–7. 10.1016/j.jbmt.2020.02.002. [DOI] [PubMed] [Google Scholar]
  • 70.Fontoura et al. Effect of the muscular strength detraining in prepubertal boys 2004.
  • 71.García-Hermoso A, Saavedra JM, Escalante Y, Domínguez AM. Effects of a long-term physical exercise program with and without diet on obese boys after six-month detraining. World J Pediatr. 2014;10:38–45. 10.1007/s12519-014-0451-7. [DOI] [PubMed] [Google Scholar]
  • 72.Zacca R, Toubekis A, Freitas L, Silva AF, Azevedo R, Vilas-Boas JP, et al. Effects of detraining in age-group swimmers performance, energetics and kinematics. J Sports Sci. 2019;37:1490–8. 10.1080/02640414.2019.1572434. [DOI] [PubMed] [Google Scholar]
  • 73.Faigenbaum AD, Farrell AC, Fabiano M, Radler TA, Naclerio F, Ratamess NA, et al. Effects of detraining on fitness performance in 7-Year-Old children. J Strength Cond Res. 2013;27:323–30. 10.1519/JSC.0b013e31827e135b. [DOI] [PubMed] [Google Scholar]
  • 74.Nunes ACCA, Cattuzzo MT, Faigenbaum AD, Mortatti AL. Effects of integrative neuromuscular training and detraining on countermovement jump performance in youth volleyball players. J Strength Cond Res. 2021;35:2242–7. 10.1519/JSC.0000000000003092. [DOI] [PubMed] [Google Scholar]
  • 75.Santos EJ, Janeira MA. Effects of reduced training and detraining on upper and lower body explosive strength in adolescent male basketball players. J Strength Cond Res. 2009;23:1737–44. 10.1519/JSC.0b013e3181b3dc9d. [DOI] [PubMed] [Google Scholar]
  • 76.D’souza C, Avadhany ST. Effects of yoga training and detraining on physical performance measures in prepubertal children– a randomized trial. Indian J Physiol Pharmacol N D:8. [PubMed]
  • 77.Donti Ο, Papia K, Toubekis A, Donti A, Sands WA, Bogdanis GC. Flexibility training in preadolescent female athletes: acute and long-term effects of intermittent and continuous static stretching. J Sports Sci. 2018;36:1453–60. 10.1080/02640414.2017.1397309. [DOI] [PubMed] [Google Scholar]
  • 78.Chaouachi A, Ben Othman A, Makhlouf I, Young JD, Granacher U, Behm DG. Global training effects of trained and untrained muscles with youth can be maintained during 4 weeks of detraining. J Strength Cond Res. 2019;33:2788–800. 10.1519/JSC.0000000000002606. [DOI] [PubMed] [Google Scholar]
  • 79.Vianna L, Marques DL, Marques MC, Ferraz R. Physical performance changes during circuit training and detraining in U15 soccer players. J. Hum. Sport exerc.– 2020 - Spring Conf. Sports sci. Universidad de Alicante; 2020. 10.14198/jhse.2020.15.Proc3.22.
  • 80.Granacher U, Muehlbauer T, Doerflinger B, Strohmeier R, Gollhofer A. Promoting strength and balance in adolescents during physical education: effects of a Short-Term resistance training. J Strength Cond Res. 2011;25:940–9. 10.1519/JSC.0b013e3181c7bb1e. [DOI] [PubMed] [Google Scholar]
  • 81.Fournier M, Ricci J, Taylor AW et al. Skeletal muscle adaptation in adolescent boys: sprint and endurance training 1982. [DOI] [PubMed]
  • 82.Tsolakis CK, Vagenas GK, Dessypris AG. STRENGTH ADAPTATIONS AND HORMONAL RESPONSES TO RESISTANCE TRAINING AND DETRAINING IN PREADOLESCENT MALES n.d.:5. [DOI] [PubMed]
  • 83.Ingle L, Sleap M, Tolfrey K. The effect of a complex training and detraining programme on selected strength and power variables in early pubertal boys. J Sports Sci. 2006;24:987–97. 10.1080/02640410500457117. [DOI] [PubMed] [Google Scholar]
  • 84.Meylan CMP, Cronin JB, Oliver JL, Hopkins WG, Contreras B. The effect of maturation on adaptations to strength training and detraining in 11-15-year-olds: strength training in youth. Scand J Med Sci Sports. 2014;24:e156–64. 10.1111/sms.12128. [DOI] [PubMed] [Google Scholar]
  • 85.Santos AP, Marinho DA, Costa AM, Izquierdo M, Marques MC. The effects of concurrent resistance and endurance training follow a detraining period in elementary school students. J Strength Cond Res. 2012;26:1708–16. 10.1519/JSC.0b013e318234e872. [DOI] [PubMed] [Google Scholar]
  • 86.Santos A, Marinho D, Costa A, Izquierdo M, Marques M. The effects of concurrent resistance and endurance training follow a specific detraining cycle in young school girls. J Hum Kinet. 2011;29A:93–103. 10.2478/v10078-011-0064-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Atay E, Kayalarli G. The effects of detraining period on female basketball team players aged 10–12 2013.
  • 88.Santos EJ, Janeira MA. The effects of plyometric training followed by detraining and reduced training periods on explosive strength in adolescent male basketball players. J Strength Cond Res. 2011;25:441–52. 10.1519/JSC.0b013e3181b62be3. [DOI] [PubMed] [Google Scholar]
  • 89.Faigenbaum AD, Westcott2 WL, Micheli LJ, Outerbridge AR, Long CJ, LaRosa-Loud R, et al. The effects of strength training and detraining on children. J Strength Cond Res. 1996;10:109. 10.1519/1533-4287(1996)010%3C0109:TEOSTA%3E2.3.CO;2.
  • 90.Zamani M, Peeri M, Farzanegi P, Rakhshanizadeh A, Piri E. The influences of muscular strength detraining in elementary school students 2012.
  • 91.Gavanda S, Geisler S, Quitmann OJ, Bauhaus H, Schiffer T. Three weeks of detraining does not decrease muscle thickness, strength or sport performance in adolescent athletes. Int J Exerc Sci. 2020;13:633–44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Alvurdu S, Baykal C, Akyildiz Z, Şenel Ö, Silva AF, Conte D, et al. Impact of prolonged absence of organized training on body composition, neuromuscular performance, and aerobic capacity: A study in youth male soccer players exposed to COVID-19 lockdown. Int J Environ Res Public Health. 2022;19. 10.3390/ijerph19031148. [DOI] [PMC free article] [PubMed]
  • 93.Aphamis G, Ioannou Y, Giannaki CD. Physical fitness and obesity levels during an academic year followed by summer holidays: an issue of insufficient time for physical activity. Int J Adolesc Med Health. 2017;31. 10.1515/ijamh-2016-0137. [DOI] [PubMed]
  • 94.De Andrade Goncalves EC, Augusto Santos Silva D, Gimenes Nunes HE. Prevalence and factors associated with low aerobic performance levels in adolescents: A systematic review. Curr Pediatr Rev. 2015;11:56–70. 10.2174/1573396311666150501003435. [DOI] [PubMed] [Google Scholar]
  • 95.Watson A, Maher C, Golley R, Dumuid D, Manson A, Tomkinson G, et al. Children’s activity and diet behaviours in the summer holidays versus school year. Pediatr Obes. 2023;18:e13029. 10.1111/ijpo.13029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Volmut T, Pišot R, Planinšec J, Šimunič B. Physical activity drops during summer holidays for 6- to 9-Year-Old children. Front Public Health. 2021;8:631141. 10.3389/fpubh.2020.631141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Barbieri A, Fuk A, Gallo G, Gotti D, Meloni A, La Torre A, et al. Cardiorespiratory and metabolic consequences of detraining in endurance athletes. Front Physiol. 2024;14:1334766. 10.3389/fphys.2023.1334766. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98.Matos N, Winsley RJ. Trainability of young athletes and overtraining n.d. [PMC free article] [PubMed]
  • 99.Spittaels H, Van Cauwenberghe E, Verbestel V, De Meester F, Van Dyck D, Verloigne M, et al. Objectively measured sedentary time and physical activity time across the lifespan: a cross-sectional study in four age groups. Int J Behav Nutr Phys Act. 2012;9:149. 10.1186/1479-5868-9-149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Malina RM, Bouchard C, Bar-Or O. Growth, maturation, and physical activity. Human Kinetics; 2004.
  • 101.Lloyd RS, Oliver JL. The youth physical development model: A new approach to Long-Term athletic development. Strength Cond J. 2012;34:61–72. 10.1519/SSC.0b013e31825760ea. [Google Scholar]
  • 102.Rogol AD, Clark PA, Roemmich JN. Growth and pubertal development in children and adolescents: effects of diet and physical activity. Am J Clin Nutr. 2000;72. 10.1093/ajcn/72.2.521S.:521S-528S. [DOI] [PubMed]
  • 103.Viru A, Loko J, Harro M, Volver A, Laaneots L, Viru M. Critical periods in the development of performance capacity during childhood and adolescence. Eur J Phys Educ. 1999;4:75–119. 10.1080/1740898990040106. [Google Scholar]
  • 104.Akbar S, Soh KG, Jazaily Mohd Nasiruddin N, Bashir M, Cao S, Soh KL. Effects of neuromuscular training on athletes physical fitness in sports: A systematic review. Front Physiol. 2022;13:939042. 10.3389/fphys.2022.939042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Armstrong N, van Mechelen W, editors. Oxford textbook of children’s sport and exercise medicine: access content online at Oxfordmedicine.com. Third edition. Oxford: Oxford University Press; 2017. [Google Scholar]
  • 106.Bosquet L, Berryman N, Dupuy O, Mekary S, Arvisais D, Bherer L, et al. Effect of training cessation on muscular performance: A meta-analysis. Scand J Med Sci Sports. 2013;23. 10.1111/sms.12047. [DOI] [PubMed]
  • 107.Rumpf MC, Cronin JB, Oliver J, Hughes M. Kinematics and kinetics of maximum running speed in youth across maturity. Pediatr Exerc Sci. 2015;27:277–84. 10.1123/pes.2014-0064. [DOI] [PubMed] [Google Scholar]
  • 108.Massidda M, Miyamoto N, Beckley S, Kikuchi N, Fuku N. Genetics of flexibility. Sports Exerc Nutr Genomics. 2019;273–93. 10.1016/B978-0-12-816193-7.00013-0.
  • 109.Thieschäfer L, Büsch D. Development and trainability of agility in youth: A systematic scoping review. Front Sports Act Living. 2022;4:952779. 10.3389/fspor.2022.952779. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

40798_2025_883_MOESM1_ESM.docx (140.7KB, docx)

Supplementary Material 1: Appendix S1 - Search strategy for each database.

40798_2025_883_MOESM2_ESM.xlsx (10.9KB, xlsx)

Supplementary Material 2: Appendix S2 - Data extraction of studies on lockdown

40798_2025_883_MOESM3_ESM.xlsx (85KB, xlsx)

Supplementary Material 3: Appendix S3 - Data extraction of studies on school vacations

40798_2025_883_MOESM4_ESM.xlsx (46.1KB, xlsx)

Supplementary Material 4: Appendix S4 - Data extraction of studies on training cessation

40798_2025_883_MOESM5_ESM.xlsx (92.9KB, xlsx)

Supplementary Material 5: Appendix S5 - Quality assessment of pre-post studies with no control groups

40798_2025_883_MOESM6_ESM.xlsx (14KB, xlsx)

Supplementary Material 6: Appendix S6 - Quality assessment of controlled intervention studies

40798_2025_883_MOESM7_ESM.xlsx (13.5KB, xlsx)

Supplementary Material 7: Appendix S7 - Quality assessment of cross-sectional and cohort studies

40798_2025_883_MOESM8_ESM.xlsx (13.9KB, xlsx)

Supplementary Material 8: Appendix S8 - Summary of tests employed in studies and their frequency of use

40798_2025_883_MOESM9_ESM.xlsx (15.2KB, xlsx)

Supplementary Material 9: Appendix S9 - Effect of disruptions in boys, girls and mixed groups

Supplementary Material 10 (238.4KB, jpg)

Data Availability Statement

The data used to support the findings of this study are included within the article and the supplementary information file.


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