Abstract
Resistance training (RT) is widely regarded as the gold standard approach for enhancing muscular fitness (i.e., muscle strength, power, and muscular endurance) in youth while also providing health and physical fitness benefits traditionally associated with aerobic training (e.g., enhanced cardiorespiratory fitness, reduced body fat, improved insulin sensitivity). Additionally, while bone health can be improved following RT (particularly after plyometric jump training), aerobic training may result in a lesser or even neutral impact on bone mineral density enhancement (e.g., swimming). Regarding mental health and cognition, while aerobic training has well-established positive effects, preliminary evidence in obese youth suggests that RT may offer greater benefits in certain aspects compared to aerobic training. Additionally, RT can reduce the risk and incidence of injuries in youth. Overall, we argue in this Current Opinion article that the current consideration of RT as an additional, rather than essential (possibly even the most essential), aspect of physical activity in current national and international guidelines needs to be reconsidered. Overall, there is an urgent need to inform relevant stakeholders that, while aerobic activities remain essential, the next generation of physical activity guidelines should place greater emphasis on the particular importance of RT, providing more comprehensive guidance on its implementation for youth.
Key Points
| The current physical activity guidelines, which state that youth should engage in at least an average of 60 min of moderate-to-vigorous, mostly aerobic physical activity daily with vigorous-intensity aerobic activities, as well as muscle and bone strengthening exercises, carried out at least three times weekly as part of the 60 min of daily activity, seem to emphasize aerobic over muscle strengthening exercises (i.e., resistance training). |
| Promoting resistance training is paramount to combat the widespread effects of physical inactivity, improving muscular fitness, and reducing activity-related injuries as well as adverse health events in youth. |
| Resistance training can also yield adaptations typically associated with aerobic training, such as enhanced cardiorespiratory fitness, reduced body fat, and increased insulin sensitivity. Indeed, while aerobic training alone cannot entirely replace resistance training in youth, resistance training appears to provide some level of substitution. |
| There is an urgent need to update the current hierarchy of physical activity guidelines for youth by prioritizing resistance training and providing clearer recommendations on dosage. However, this shift would not minimize the benefits of aerobic training, particularly the potential synergistic effects of combining resistance and aerobic training. |
Introduction
After decades of questioning the safety and efficacy of resistance training (RT) in youth (an umbrella term for children and adolescents [1]) [2], extensive and persuasive evidence to the contrary has now emerged, starting with a seminal review by Kraemer et al. [3] and subsequent publications [4–14]. Of note, RT is a specialized method of physical conditioning that involves the progressive application of varying resistive loads, movement velocities, and training modalities including equipment such as weight machines, free weights (barbells and dumbbells), elastic bands, medicine balls, and plyometric1[15] exercises [6]. There is now a widespread consensus that RT is safe, effective, and an irreplaceable tool to promote both physical fitness2[16] and health in youth. Indeed, the benefits of RT cover a wide range of health aspects such as strength [17, 18], bone mass/bone mineral density (BMD) [19–24], body composition [23, 25–28], mental health [23, 26], and cognitive function [26, 29]. Additionally, RT may aid in preventing negative health outcomes in youth such as type 2 diabetes [24, 26, 30], cardiovascular diseases [23, 26, 31, 32], as well as premature death [33]. Furthermore, it is well known that RT improves muscular fitness (i.e., muscle strength, muscle power, and muscular endurance) in youth [25, 34–36]. However, despite the remarkable, well-established benefits of RT, the adherence rate to physical activity (PA), including RT, among youth is alarmingly low. Evidence derived from a pooled analysis of 298 population-based surveys including 1.6 million participants indicates that 81% of youth aged between 11 and 17 years fail to adhere to the World Health Organization (WHO)’s PA guidelines and are thus classified as physically inactive [37]. This is consistent with other studies including those with large sample sizes [38, 39]. This reflects a widespread global trend of physical inactivity3 and sedentary behaviour among youth [40]. Given the well-established tracking character of PA and muscular fitness [24, 41–43], not only short but also long-term negative consequences on physical fitness and health can be expected.
Established public health institutions, including the United States Department of Health and Human Services [23] and the WHO [44], communicate recommendations for PA to the public. These guidelines represent a crucial source of information for youth themselves, their parents, policy-makers, and healthcare professionals [9]. As such, the accuracy of such guidelines with respect to the available evidence is of utmost importance to promote healthy behaviours [45]. The most up-to-date PA guidelines by the WHO indicate that youth should engage in at least an average of 60 min of moderate-to-vigorous, primarily aerobic4 PA daily [44]. Additionally, within these 60 min, vigorous-intensity aerobic activities as well as muscle- and bone-strengthening exercises should be carried out at least three times weekly [44]. In particular, these recommendations emphasize the amount of aerobic PA that should be accumulated across the week. However, the early development of muscle strength in youth is of utmost relevance [46]. It is noteworthy that a low level of muscle strength in youth, referred to as paediatric dynapenia, can have severe consequences pertaining to the development of functional limitations (i.e., impaired fundamental movement skills5[47]), physical inactivity and sedentary behaviour, as well as an increased risk of negative health events (e.g., higher risk of injuries and chronic diseases) [4, 7, 10, 12].
While the significance of aerobic training in preventing chronic diseases in youth is undeniable [23], RT can be equally effective as aerobic training, such as in preventing type 2 diabetes [48, 49]. For instance, Grøntved et al. [48] investigated the association of muscle strength and cardiorespiratory fitness with indices of glucose metabolism in healthy youth, followed over 12 years. The findings indicated similar levels of association between muscle strength and cardiorespiratory fitness with both insulin resistance and β-cell function. The authors concluded that muscle strength is similarly effective as cardiorespiratory fitness in preserving healthy insulin sensitivity and β-cell function later in life [48]. Notably, these associations were independent of adiposity and demographic, personal, and lifestyle factors [48]. Therefore, early engagement in aerobic or RT substantially and similarly reduces the risk of impaired insulin sensitivity and improves β-cell function in later years. Lee et al. [49] examined the effects of three months' RT versus aerobic training on abdominal adiposity, ectopic fat, and insulin sensitivity in obese male youth. Their findings revealed similar reductions in abdominal fat and intrahepatic lipid across both training modalities, but RT (unlike aerobic training) was associated with significant improvements in insulin sensitivity. Additionally, there are indications that the adherence rate differs between RT and aerobic training in youth. Indeed, 50.7% met the guidelines for muscle-strengthening (e.g., exercises to strengthen or tone the muscles such as push-ups, sit-ups, and weight lifting), 70.6% met the vigorous aerobic PA guidelines, and 80.7% met those for bone-strengthening, but overall only 15.2% adhered to the moderate-to-vigorous, mostly aerobic PA guidelines [50] as per the United States Physical Activity guidelines [51]. These findings are supported by other studies [52, 53]. However, caution is warranted when interpreting these results, as differing standards are applied to assess adherence to each type of PA. Specifically, meeting the criterion of engaging in RT at least 3 days per week is considerably easier than achieving an average of 60 min of aerobic moderate-to-vigorous PA daily. Furthermore, weaker youth often lack the ability, confidence, and motivation to engage in exercise and sports activities, increasing the likelihood of adopting a sedentary behaviour/lifestyle [7, 24, 54–56]. Early exposure to RT has the potential to counteract this trend by fostering strength, confidence, and competence. This foundation can enable youth to engage in and sustain regular PA, thereby improving adherence to PA guidelines [7, 9, 56]. Therefore, RT could be considered a more effective approach than aerobic training, particularly in helping to mitigate the widespread issue of physical inactivity among youth. Another potential advantage of RT is that it may be more preferred than aerobic training. Evidence suggests that RT is more enjoyable than aerobic training (e.g., running, cycling) in youth, particularly those who are overweight or obese [25, 57, 58]. While direct comparisons in healthy youth are lacking, we speculate that similar outcomes may be observed in this population.
In this Current Opinion article, we argue that the current PA recommendations’ hierarchy that emphasizes aerobic over RT needs to be revised. Specifically, we call for reversing the current priority framework by prioritizing RT, without disregarding the complementary effects of combining it with aerobic training. Previous review papers have underscored the importance of RT in adults and older adults [8, 59]. In youth, however, the sole available study by Faigenbaum et al. [9] emphasized the significance of RT in youth for enhancing physical fitness and health, and advocated for prioritizing muscular fitness development in youth guidelines. Nonetheless, a comprehensive description of the health benefits of RT is still lacking, and studies comparing aerobic training and RT have not been thoroughly summarized. Therefore, this Current Opinion article aims to synthesize the available evidence regarding the effects of RT compared to aerobic training on physical fitness and health outcomes in youth and to advocate for greater emphasis on RT for youth in the next generation of PA guidelines.
The Compound Threat of Paediatric Dynapenia
Paediatric dynapenia is one of the leading contemporary threats to health among youth [7, 10, 60, 61]. The term dynapenia has been adopted from the literature relating to geriatric patients and stands for decreased levels of muscle strength and power not caused by neurological or muscular disease [10, 61], meaning that paediatric dynapenia is identifiable and treatable. The alarmingly low adherence rate to PA among youth worldwide [37–39] appears to be the main driver of the secular decline in measures of muscular fitness and, therefore, dynapenia [62–64]. In a recent study investigating the secular trend of physical fitness among a large sample of Chinese rural youth, Li et al. [62] reported increased muscle strength and power from 1985 to 2000. However, this positive trend has reversed from 2000 to 2010, marked by a decline in muscle strength and power. Notably, this decline persisted through the subsequent period from 2010 to 2019 [62]. In fact, the secular decline in muscular fitness among youth has been consistently reported by other studies [65–69], though this trend does not apply to all measures of physical fitness, such as handgrip strength [70]. Indeed, a 3-year longitudinal study demonstrated that physical fitness, including muscular fitness, is significantly correlated with the time spent in moderate-to-vigorous PA in youth [64]. Additionally, a systematic review of the literature by Smith et al. [71] supported the positive correlation among youth between PA and muscular fitness, specifically vigorous PA and organized sports participation. Recently, Fraser et al. [72] revealed that PA is one of the key factors leading to better muscle strength in the long term.
Physical fitness, particularly muscle strength, is considered a powerful marker of health [19, 24, 73–76]. Cumulative evidence suggests that the current generations of youth are weaker than previous ones [62, 65–67], indicative of a growing trend in paediatric dynapenia. It is worth noting that the relationship between paediatric dynapenia (muscle weakness) and PA is bidirectional. While we acknowledge that paediatric dynapenia generally develops as a result of physical inactivity in healthy youth, there are also cases when dynapenia precedes physical inactivity, particularly in unhealthy youth. For instance, congenital or neuromuscular disorders in youth may result in primary muscle weakness, leading to reduced PA [77–79]. Once it occurs, paediatric dynapenia leads to a cascade of severe negative consequences, including increased functional limitations and decreased fundamental movement skills in youth [7, 9, 10, 54, 60, 61]. Weaker youth may lack the ability, confidence and motivation to engage in exercise and sports activities, increasing the likelihood of adopting a sedentary behaviour [7, 24, 54, 55]. This tendency is further accentuated by the availability of sedentary alternatives like screen time and video games [9, 43, 80]. As a result, these youths are more exposed to adverse health outcomes caused by muscle disuse and physical inactivity [81, 82], a trend that has been demonstrated in numerous studies [31, 83]. Earlier studies have shown that muscle strength in adolescent males is inversely correlated with cardiovascular disease events and mortality in middle age, regardless of cardiorespiratory fitness and other confounding factors such as smoking and alcohol consumption [31]. Moreover, in a large cohort of 1.2 million males, Henriksson et al. [83] revealed that muscle weakness is associated with disability 30 years later.
Persuasive evidence indicates that PA [84–87], physical fitness [41, 42], and more particularly muscle strength [42, 88] track from childhood to adulthood. Therefore, it is plausible to argue that paediatric dynapenia also tracks from early to later ages. Fraser et al. [88] investigated the track of muscle strength from youth to adulthood in a sample of 1207 participants and reported a significant tracking correlation ranging from 0.47 to 0.72. The results of another prospective cohort study including 623 participants corroborate the previous findings indicating a relatively stable muscle strength and power between youth and adulthood with a tracking correlation ranging from 0.43 to 0.47 [42]. Additionally, inactive youth tend to become resistant to exercise interventions later in life [89], emphasizing the utmost need for structured and systematic programs aiming at combating strength deficits in youth. This needs to be undertaken at an early age to develop a routine pattern of healthy PA behaviour, including RT, that will persist to later stages in life. Evidence suggests that RT can be started from the age of 7–8 years, or even earlier, depending on individual readiness, provided the youth can understand/follow instructions and is able to demonstrate proper movement technique [7, 14, 90, 91]. Key considerations when introducing RT to youth include prioritizing technique, supervision by qualified trainers, and ensuring the program is age-appropriate [90, 92, 93].
Taken together, paediatric dynapenia must be actively prevented and early proactive measures should be undertaken to avoid its occurrence. Current public health recommendations for youth advocate engaging in at least an average of 60 min of moderate-to-vigorous, mostly aerobic PA daily, with vigorous-intensity aerobic activities as well as muscle- and bone-strengthening activities incorporated at least 3 days a week as part of the 60-min activity [44]. However, these guidelines primarily emphasize the amount of aerobic PA, while placing less focus on the critical importance of muscle-strengthening exercises. It is crucial to recognize that promoting muscle strength through RT is paramount for combating physical inactivity, improving fundamental movement skills, and reducing activity-related injuries as well as adverse health events. As such, while we acknowledge the importance of aerobic training, there is a pressing need to shift the focus in the next generation of PA guidelines towards RT and to provide more detailed guidelines related to its dosage.
The Effects of Resistance Training versus Aerobic Training on Health Outcomes in Youth
Chronic Diseases
Recently, Brellenthin et al. [59] indicated that RT is as beneficial as aerobic training for several health issues such as type 2 diabetes, cancer, cardiovascular disease, and obesity, among adults. The same authors emphasized that individuals who perform both RT and aerobic training would experience the greatest health benefits, reflecting a synergistic effect on health-related outcomes [59]. In youth populations, studies that directly contrasted the association of RT and aerobic training with key health outcomes are scarce [49, 94, 95]. Additionally, most of the studies compared the association of RT and aerobic training with changes in health outcomes such as insulin sensitivity and body fat in overweight and obese youth [49, 95–98]. For example, Lee et al. [49] investigated the effects of 3 months of RT versus aerobic training on abdominal adiposity, ectopic fat, and insulin sensitivity in obese male youth, revealing similar reductions in abdominal fat and intrahepatic lipid, although only RT was associated with marked improvements in insulin sensitivity. In a randomized controlled trial, Sigal et al. [97] compared RT, aerobic training, and combined training effects on body composition and cardiometabolic risk factors in overweight and obese youth, revealing similar decreases in percentage body fat and waist circumference following RT and aerobic training. However, combined RT and aerobic training exerted a synergistic effect on the same outcomes [97]. In a similar study in overweight and obese adolescents, Lee et al. [98] examined the effects of RT, aerobic training, or combined training on insulin sensitivity, total adiposity, and ectopic fat in overweight and obese adolescents and reported that all training modalities were beneficial in reducing body fat and intermuscular adipose tissue, as well as enhancing insulin sensitivity. They specifically reported that combined RT and aerobic training as well as aerobic training alone were similarly effective in reducing ectopic fat in the liver and skeletal muscle [98]. Moreover, these training modalities also increased insulin sensitivity, but aerobic training was relatively more effective by approximately 41% than RT regarding the improvement of insulin sensitivity [98]. Inoue et al. [99] conducted an intervention study including obese youth and concluded that combined RT and aerobic training was more effective than aerobic training alone to improve lipid profile and insulin sensitivity. In the same context, Goldfield et al. [94] contrasted the effects of 22 weeks of RT versus aerobic training versus combined training on health-related quality of life (measured using the Paediatric Quality of Life Questionnaire) in overweight and obese youth of both sexes. The results indicated that both RT and aerobic training alone improved health-related quality of life but that combined RT and aerobic training generated the largest improvements relative to the control group. Furthermore, Dâmaso et al. [100] demonstrated that 1 year of combined RT and aerobic training was more effective than aerobic training alone in improving visceral adiposity, metabolic profile, and inflammatory markers in obese youth. Moreover, in a critical summary of the available evidence, Lee et al. [101] concluded that single-mode RT is associated with a significant decrease in total fat and insulin resistance in previously sedentary obese youth. In summary, accumulating evidence indicates that the health benefits of RT are similar to those of aerobic training concerning total adiposity, cardiometabolic risk, and insulin resistance. Additionally, the combination of both training modalities seems to provide synergistic effects in overweight and obese youth.
In healthy youth, however, investigations that directly compared the impact of RT, aerobic training, or combined training on important health-related outcomes are scarce. Emerging evidence indicates that muscle strength is also associated with cardiovascular health [31, 102]. Specifically, muscle strength in adolescent males is inversely associated with later cardiovascular disease events and mortality in middle age, independent of cardiorespiratory fitness and other confounding variables (e.g., smoking, alcohol consumption) [31]. Additionally, Åberg et al. [102] conducted a prospective cohort study including ~ 1.5 million Swedish male conscripts over 42 years. The study aimed to examine whether aerobic fitness or muscle strength registered at a young age (18 years), independently or combined, correlate with long-term stroke risk [102]. Low aerobic fitness in youth and high stroke incidence during adulthood were noted, with a hazard ratio (HR) of up to 1.70, i.e. 70% increased risk for those with low aerobic fitness at a young age [102]. However, the investigators also revealed that low muscle strength in youth was associated with increased stroke incidence during adulthood, with an HR of 1.39 (1.17 after accounting for aerobic fitness) in the low muscle strength group compared with the high muscle strength group, pointing towards the independent nature of the association between muscle strength in youth and stroke risk later in life [102]. In a prospective cohort study including ~ 1 million male adolescents, Ortega et al. [33] revealed that those with a muscle strength performance equal to or above the 40th percentile of the studied population displayed a 20% lower risk of all causes of premature death and 25% lower risk of cardiovascular disease than those in the 10th percentile. Additionally, for each 5% decrease in muscle strength, there was a 1.48 increased odds of high cardiometabolic risk in youth males and a 1.45 increase in females [103]. Furthermore, Artero et al. [104] demonstrated that metabolic risk in youth was independently associated with both muscular and cardiorespiratory fitness. Other studies [105, 106] clearly indicate that a low level of muscle strength is one of the contributing factors to metabolic dysfunction in youth. Henriksson et al. [83] conducted a prospective cohort study with ~ 1.2 million participants to investigate the associations between muscle strength in adolescence with later disability pension. Disability pension is granted if an individual is likely to never work full-time again due to severe chronic disease or injury. The authors reported a strong association between muscular weakness and disability 30 years later [83]. They also found that the combination of low muscle strength and low aerobic fitness was a prominent risk factor for disability [83]. Furthermore, the findings indicated that being unfit, weak and obese exhibited the highest association with disability pension risk (HR = 3.70, 95% confidence interval (CI) = 2.99 to 4.58) [83]. Of note, correlation (e.g., prospective cohort studies) does not directly imply causation, and this should be taken into consideration [107].
Overall, compelling evidence suggests that low muscle strength results in adverse health outcomes for both the present and the future health of youth. These outcomes include an increasing risk of developing metabolic dysfunction, cardiovascular diseases, and insulin resistance [32, 97, 99, 102, 103, 106, 108–112]. More specifically, accumulating evidence indicates that RT generates beneficial effects on health outcomes traditionally attributed solely to aerobic training. While aerobic training might outperform RT in preventing cardiovascular diseases [102], both RT [48, 49] and aerobic training [48, 98] can lead to improved insulin sensitivity. Combining both training modalities appears to have synergistic effects on numerous health-related outcomes [48, 94, 97, 99, 100]. However, it is imperative to conduct additional high-quality studies that directly compare the effects of RT and aerobic training on key health outcomes, particularly in healthy youth. Given the limited literature in this area, this is essential to enhance our understanding. Furthermore, exploring the physiological mechanisms that underpin the link between RT and improvements in diverse health outcomes in youth presents significant opportunities for future research.
Bone Health
Growing bones around puberty are more sensitive to mechanical loading compared to adults’ bones [113], making this age period optimal for improving bone health in youth [20, 114–116]. The benefits to bone health arise from the synergistic interaction between the natural growth-related increase in bone mass and mechanical loading, particularly induced by RT [20]. Indeed, the American College of Sports Medicine proposed two main strategies to maintain and/or improve bone health: (i) maximizing BMD during the first 30 years of life, and (ii) mitigating the decrease in BMD after 40 years [117]. Increasing BMD during childhood and adolescence is the most appealing strategy, as this will track into adulthood, reducing the risk of fractures at a later age [113, 114, 118–121]. Moreover, peak bone mass during puberty and early adulthood is a powerful predictor of the risk of osteoporosis in older age in females [119]. Therefore, given the track character of bone health, it seems imperative to implement effective interventions to enhance bone health from an early age. This proactive approach can help to mitigate the risk of osteoporosis and fractures later in life, especially in females [122].
Muscle strength and mass are considered key predictors of bone health [32, 123]. Sioen et al. [124] conducted a systematic review of observational and longitudinal studies that examined the correlation between muscle mass and bone parameters in youth. They reported that most investigations showed positive associations between muscle mass and BMD, bone mineral content (BMC), and bone area [124]. Additionally, a consistent positive relationship between muscle strength in youth and bone parameters has been reported in the literature [32]. For example, significant positive associations between handgrip strength and BMD as well as BMC at the hip, spine and entire body have been reported, regardless of children’s sex [125]. The same authors concluded that handgrip strength could be considered an independent predictor of BMD and BMC in children [125]. This conclusion was supported by other studies in youth [126–129].
Different types of RT, such as machine-based and free-weight RT, can benefit BMD in youth [114]. More particularly, high-impact or jump-based exercises that create sufficient ground reaction forces (GRFs) are considered the most prominent RT modality to promote osteogenic processes and improve bone health in youth [21, 113, 114, 117, 130–135]. More specifically, plyometric jump training may have the potential to maximize bone mineralization when applied during the pubertal growth spurt [136]. Indeed, jump-based exercises with GRFs ranging from 3.5 to 8.8 of one’s own body mass conducted for 10 min two to three times per week are effective in enhancing BMD among children and adolescents [137]. This suggests that for bone adaptations, the intensity of RT is a key factor and long-duration training sessions are not required. Gómez-Bruton et al. [138] conducted a systematic review of the effects of plyometric jump training on bone health in youth, and revealed that out of the 26 included studies, 24 demonstrated improved bone health, reflecting widespread consensus in the literature. The same authors concluded that plyometric jump training during childhood and adolescence has the potential to foster BMC, density BMD, and structural properties without side effects [138]. Ishikawa et al. [21] conducted a meta-analysis, and reported that high-impact weight-bearing activities (e.g., plyometric jump training) induced the largest benefits on bone mineral accrual in prepubertal females.
While aerobic PA could increase BMD [114, 139], the effects are generally lower than those generated by RT [114, 140, 141]. Furthermore, some types of aerobic exercise, specifically non-weight-bearing activities such as swimming and cycling may have a lesser or even neutral impact on BMD enhancement [114, 142–146]. Therefore, to optimize bone health, these activities should ideally be complemented by RT exercises designed to stimulate bone strength and density. This appears to be due to the relatively low mechanical stimulus during swimming and cycling, which is still below the threshold for positive osteogenic effects [128–130]. Ribeiro-Dos-Santos et al. [145] showed that the prolonged practice of swimming can negatively affect BMD gains in adolescents. Indeed, swimmers train in a hypogravitational environment where muscles do not have to counteract gravity, resulting in a low mechanical stress—a crucial factor that promotes BMD improvement [131, 132].
In summary, peak bone mass is typically attained during the developmental period, around puberty [115]. Therefore, improving bone health at an early age has a positive lifelong impact on future bone health. RT, particularly plyometric jump training, yields substantial positive effects on bone health in youth. Conversely, aerobic training appears to be less effective and may even have deleterious effects on bone health [114, 146].
Mental Health/Cognitive Function
The results of a cross-sectional study aiming at investigating the independent and joint associations of RT and aerobic training with mental health in adolescents indicated that meeting either the RT or aerobic PA guidelines alone led to a lower prevalence of ever feeling sad or hopeless and difficulty making decisions [147]. Additionally, meeting both recommendations was more strongly associated with fewer mental health problems [147].
Goldfield et al. [57] conducted a randomized controlled trial on the effects of 6 months' RT versus aerobic training versus combined training versus no training on mood, self-esteem and body image of obese male and female adolescents. The authors revealed that only RT reduced depressive symptoms and that combined training led to greater improvement in vigour compared with the control group. Additionally, only RT improved global self-esteem and only RT and combined training enhanced perceived strength compared to the control group [57]. Therefore, RT offers psychological benefits among adolescents with obesity, thus presenting a potential exercise alternative for youth who find aerobic training uncomfortable or unenjoyable [57]. Recently, Chiang et al. [148] conducted a large cohort study including 1.9 million youth to examine the association between physical fitness and the risk of mental disorders. They reported that youth in higher fitness quantiles exhibited lower cumulative incidences of anxiety disorders, depressive disorders, and attention-deficit/hyperactivity disorder. Specifically, Chiang et al. [148] demonstrated that improvements in both muscular fitness, particularly muscular power and endurance (commonly achieved through RT), and cardiorespiratory fitness (typically resulting from aerobic training), were independently associated with reduced prevalence of mental health disorders in youth. The authors concluded that muscular and cardiorespiratory fitness could be considered protective factors against the onset of mental disorders in youth [148]. Eather et al. [149] conducted a randomized controlled trial to explore the impact of the CrossFit™ Teens RT on the mental health of adolescents, and revealed enhanced mental well-being in adolescents at risk of psychological disorders. Collins et al. [150] conducted a systematic review with meta-analysis on the effects of RT on the “self” (i.e., self-esteem, self-efficacy and self-perception) in youth, reporting improved RT self-efficacy, perceived physical strength, physical self-worth, and global self-worth. Furthermore, Robinson et al. [29] carried out a systematic review with meta-analysis investigating the effect of RT on academic outcomes in school-aged youth, and demonstrated that RT resulted in positive effects, although small in magnitude, on the combined outcomes of cognition, academic achievement, and on-task behaviour. In addition, findings indicated that RT was more effective than concurrent training (i.e., combined RT and aerobic training) and that higher levels of muscular fitness were associated with better performance in tests of cognition and academic achievements in the same population [29]. Albeit not well explored yet, there are indications that the increased cognitive demands of RT appear to support improvements in cognition and academic outcomes, potentially through mechanisms such as neurogenesis [151].
In summary, while the beneficial effects of aerobic training (particularly high-intensity interval training) on mental health and cognition in youth are undeniable [148, 152–155], preliminary evidence, primarily in obese youth, suggests that RT may offer greater benefits in certain aspects compared to aerobic training [57]. In particular, RT seems to be more enjoyable than aerobic training (e.g., running, cycling) in youth, especially for overweight and obese youth [25, 57, 58]. Future studies comparing the effects of RT and aerobic training on mental health and cognitive performance in youth are warranted to confirm the preliminary findings in obese youth and to explore their effects in healthy youth, a topic that has not been thoroughly investigated yet. Additionally, the neurophysiological mechanisms underlying RT-related cognitive adaptations in youth remain to be fully understood.
Injury Prevention
RT is a well-established powerful injury prevention strategy in youth [6, 12, 54, 156, 157]. Generally, there is compelling evidence that youth with low levels of physical fitness, including muscle strength, and poor movement competency are more exposed to injuries [158–160].Torres Martín et al. [161] investigated the effects of 15 weeks of body mass-based RT on musculotendinous injury incidence and burden in U16 male soccer players. Albeit not significant, they reported a decreased musculotendinous injury incidence in the intervention compared to the control group (1.19 vs. 1.40 injuries/1000 h of exposure, respectively) [161]. Moreover, body mass RT significantly reduced injury burden, defined as the number of days lost per 1000 h of exposure (33.28 [control group] vs. 9.55 [intervention group]), indicative of a decreased severity of musculotendinous injuries in the RT compared to the control group [161]. Collard et al. [158] investigated the impact of a school-based PA program (encompassing strength, speed, flexibility, and coordination exercises) on injuries occurring during physical education sessions among primary school children aged 10–12 years. Their findings revealed a significant decrease in the rate of PA-related injuries, particularly notable among the least physically active children, with an HR of 0.47 (53% reduction in total injuries observed).
Neuromuscular training is an umbrella term that covers general (e.g., fundamental movement skills) and specific (e.g., sport-specific actions) strength and conditioning activities such as resistance, balance, core strength, plyometric and agility exercises [1]. The findings of a meta-analysis including 25 studies examining the effects of neuromuscular training reported ~ 36% reduction in lower limb incidence rate ratio in youth team sport [162], consistent with earlier reviews [163–166]. The preventive effects (68% risk reduction) of neuromuscular training on anterior cruciate ligament injuries in female athletes have also been highlighted in the meta-analysis by Sugimoto et al. [167]. Moreover, in another meta-analysis, Steib et al. [168] reported that neuromuscular training resulted in a 42% injury rate reduction in youth athletes.
In sum, RT and neuromuscular training are effective strategies to reduce the risk and rate of injuries in youth athletes as well as youth from the general population. The neural adaptations associated with RT (e.g., enhanced neural drive) and structural/mechanical changes (e.g., hypertrophy, increased musculotendinous stiffness) improve movement biomechanics, which is one of the key mechanisms underlying the reduced risk and incidence of injuries following RT [6]. Additionally, increased muscle strength and endurance, reflecting a higher fitness level, can help reduce the likelihood of fatigue-related injuries [169, 170]. Furthermore, enhanced joint stability, better balance and proprioception, and reduced muscular imbalances are key factors contributing to the reduction in injury risk among youth following RT [169–172]. RT is a widely recognized method to improve neuromuscular function,6 regardless of age [34, 92, 173–175]. Indeed, RT improves neural (e.g., motor unit recruitment and firing rate, intermuscular coordination) and structural (e.g., muscle hypertrophy) outcomes in youth [173, 176, 177]. Aerobic training, on the other hand, is a well-known means to improve cardiorespiratory fitness in youth [44, 178–180], although a certain effect on muscle hypertrophy cannot be totally ruled out [181, 182].
The Effects of Resistance Training and Aerobic Training on Physical Fitness in Youth
Muscular Fitness
Among the various training methods, none has proven as effective in enhancing muscular fitness, particularly muscle strength and power, in youth as RT [4, 5, 7, 9, 12, 44, 61, 173, 176]. Indeed, RT can improve measures of muscle strength and power in athletic [172, 183–191] and non-athletic populations [192–196]. For instance, Lesinski et al. [197] in a systematic review with meta-analysis of 43 original studies indicated that RT generated large effects on proxies of muscle strength in trained youth. Relatedly, an umbrella review including 14 meta-analyses indicated that RT produced medium-to-large effects on muscle strength and small-to-large effects on muscle power in youth [34]. A number of renowned stakeholders (e.g., National Strength and Conditioning Association, United Kingdom Strength and Conditioning Association, Canadian Society for Exercise Physiology, British Association of Sport and Exercises Sciences) have developed evidence-based position statements on the effects of RT on muscular fitness in youth [5, 14, 176, 198]. All these position papers concluded that RT has positive effects on muscular fitness in youth, irrespective of sex. Indeed, there is a widespread consensus in the literature that RT generates positive effects on muscular fitness in youth, regardless of sex, age and maturity [4, 5, 7, 9, 12, 44].
Although not as effective as RT, aerobic training may also improve muscular fitness. For example, aerobic and RT improved leg press strength (RT, 73%, from 60 to 86%; aerobic training, 42%, from 28 to 55%) compared with the control group in obese youth adolescents of both sexes [180]. A consistent trend was noted for bench-press, seated row, grip strength and push-ups (3–5% improvements and 5–12% improvements following aerobic and RT, respectively) [180]. Recent evidence indicates that lifelong RT can counteract the age-related denervation process and concurrent atrophy of type II muscle fibers in older male individuals [199]. This could contribute to promoting the maintenance of maximal strength and rate of force development, both of which are crucial for preserving functional capacity as individuals age [199]. On the other hand, individuals engaged in lifelong aerobic training displayed a lower proportion of type II muscle fibers and greater signs of atrophic fibers [199]. This suggests that early engagement in regular PA, particularly RT, is crucial for maintaining a high level of muscle strength and power in later life. These physical attributes play a pivotal role in sustaining functional capacity and independence as individuals age.
In summary, while aerobic training can offer certain benefits for muscular fitness, especially in individuals unaccustomed to regular PA, RT remains the gold standard method for achieving significant gains in muscular fitness in youth, particularly muscle strength and power.
Neural and Muscular Adaptations
Although some degree of muscle hypertrophy can be anticipated during preadolescence [200, 201], neural adaptations during the prepubertal age usually take the lead over muscular ones in response to RT [12, 92, 173, 176, 192, 202–205]. For example, muscle strength and activation (assessed by surface electromyography and interpolated twitch technique) increased in prepubertal males and females without muscle size changes [201, 206]. The dominance of neural over muscular adaptations has largely been attributed to the low level of circulating anabolic hormones (e.g., testosterone) before maturation [207–209], although the central role of testosterone in this process has recently been questioned [210]. Once puberty takes place, muscular adaptations (i.e., muscle hypertrophy) in addition to neural ones (e.g., motor unit recruitment, rate coding) occur following RT [92, 211–214]. Therefore, differences in the magnitude of RT adaptations between pre-pubertal and post-pubertal individuals might occur. Indeed, Moran et al. [215] noted greater strength and power adaptations in postpubertal compared to prepubertal swimmers after 8 weeks of RT, hypothesizing fewer pathways of adaptation (mainly neural drive) in the prepubertal group compared to the postpubertal group (neural and morphological factors). However, the underlying mechanisms leading to different training-related adaptations between pre- and post-pubertal individuals need further exploration in similarly designed research studies. However, it is worth noting that an accelerated gain during puberty is not consistently observed across different components of muscular fitness, with variations between sexes [216]. Similarly, findings from a meta-analysis on the effects of RT according to age and maturation indicate that muscle strength increases with age and maturation, with no clear evidence of accelerated gains during puberty [213].
Of note, the heterogeneity of the assessment methods used in previous studies investigating prepubertal youth spanning from less accurate, reliable and sensitive measures (e.g., skinfolds, limb girth) to more sensitive and reliable ones (e.g., ultrasound, magnetic resonance imaging) could have hampered the interpretation of the outcomes [200]. As such, future studies in youth are needed that use more accurate methods to assess muscle hypertrophy following RT, to gain more comprehensive insights. Overall, it can be assumed that the dominance of neural adaptations during preadolescence will continue to prevail after RT, while the controversial results regarding muscular changes make it premature to conclude that this adaptation indeed takes place in this population.
The Effects of Resistance Training and Aerobic Training on Cardiorespiratory Adaptations in Youth
Aerobic training is well accepted to be the gold standard mode of training to improve markers of cardiorespiratory fitness, such as VO2max [217]. However, RT can also promote cardiorespiratory fitness. Indeed, following 3 months of training, Lee et al. [49] reported comparable cardiorespiratory fitness (i.e., VO2peak) improvements following aerobic (9.0 ± 0.9 ml/kg/min) and RT (7.6 ± 0.9 ml/kg/min) in obese male youth. However, in obese youth females, improvement was greater following aerobic training (5.17 ± 1.78 ml/kg/min) compared to RT (3.10 ± 1.69 ml/kg/min) [95]. Additionally, in obese youth of both sexes, 6 months of aerobic training improved VO2peak to a greater extent (2.7%) compared to RT (0.9%) [180]. Sammoud et al. [186] reported increased endurance performance (20-m shuttle run test) after two modes of RT, plyometric training (d = 0.71) and power training using free weights (d = 0.95), in youth male soccer players. Similarly, Wong et al. [218] reported improved aerobic endurance (YoYo Intermittent Recovery Test total distance) after 12 weeks of combined strength and power training in youth male soccer players, in line with the findings of other studies in youth [219, 220].
Although the underlying mechanisms through which RT contributes to better cardiorespiratory fitness in youth have yet to be investigated, evidence in adults suggests that RT enhances running economy [221, 222], a key factor for endurance performance [223, 224]. In this regard, Wong et al. [218] revealed a significant reduction in submaximal running cost, indicative of improved running economy, which may be attributed to enhanced mechanical efficiency following combined RT and power training in youth. Additionally, increased tendon stiffness and enhancements in measures relating to neuromechanical factors (e.g., increased force-generating capacity) have been linked to better cardiorespiratory performance [225]. This is supported by earlier research demonstrating that RT improved both tendon stiffness and force-generating capacity [226, 227], facilitating a faster transfer of force from muscles to bones and reducing energy expenditure, ultimately contributing to a better running economy [228]. In summary, while aerobic training is the most effective method for improving cardiorespiratory fitness in youth, RT also has the potential to enhance cardiorespiratory fitness in this same population. It is worth noting that there are indications that combining aerobic exercise with RT (known as concurrent training) may produce a synergistic effect, resulting in enhanced cardiorespiratory fitness compared to either single-mode resistance training or aerobic training alone [220, 229]. However, this assumption lacked consistent reporting in the literature [230]. Therefore, future studies directly comparing the effects of aerobic and RT on youths' cardiorespiratory fitness are needed.
The Era of Resistance Training as a Primary Form of Exercise for Health and Physical Fitness in Youth
Despite the dedicated efforts of various national and international health agencies, institutions, and scientists to disseminate the evidence highlighting the crucial role of PA for youth, the persistently low adherence rate to PA guidelines and the widespread trend of physical inactivity among youth raise serious concerns. While it is acknowledged that there is no single solution for such a multifactorial issue, optimizing PA guidelines by emphasizing the critical role of RT might contribute to promotion of youth physical fitness and health. Indeed, weaker youth often lack the physical ability, confidence and motivation to engage in exercise and sports activities, increasing the risk of adopting a sedentary lifestyle [7, 24, 54–56]. Early exposure to RT can help mitigate this risk by developing strength, confidence, and competence, providing a foundation for engaging in and maintaining regular PA while promoting adherence to PA guidelines [7, 9, 56].
Emerging evidence suggests that RT may yield similar or even superior health benefits compared to aerobic training, including improvements in bone health, injury prevention, mental health, and cognition [6, 12, 54, 57, 114, 140, 141, 156, 157]. Additionally, RT has the potential to improve cardiorespiratory fitness [49, 95, 180, 186, 218], albeit to a lesser extent than aerobic training [95, 180] (Fig. 1). These findings suggest that, while aerobic training cannot fully replace RT in youth, RT may offer some degree of substitution. Therefore, we would argue that the traditional priority sequence, which apparently favours aerobic exercises over RT, should be reconsidered. In this vein, there seems to be an urgent need to update the current hierarchy of physical activity guidelines for youth by prioritizing RT and providing clearer recommendations on dosing. This shift does not minimize the benefits of aerobic training, particularly the potential synergistic effects of combining RT and aerobic training [48, 94, 97, 99, 100, 220, 229, 231, 232].
Fig. 1.
The effects of resistance training versus aerobic training on physical fitness and health in youth. The number of plus (+) symbols displays the magnitude of benefits of the respective component of physical activity. “+ -”: Indicates that the effects can be positive or neutral depending on the type of aerobic activity. BMD bone mineral density, BMC bone mineral content, %BF percentage of body fat, VO2max maximal oxygen uptake
It is worth noting that performing RT exercises with proper techniques in youth is a top priority. While compelling evidence supports the safety of RT in this population [6, 205, 233], the risk of injury increases when technical proficiency is lacking, training loads are inappropriate, or supervision by qualified adults is absent [6, 93, 205]. Myer et al. [234] investigated RT-related injuries presented to US emergency rooms, with respect to age, type and mechanism. They concluded that the majority of youth RT injuries resulted from accidents that could potentially be prevented with improved supervision and the implementation of stricter safety guidelines [234]. In this sense, developing RT skill competency is essential, as it provides the foundation for safe and progressive training in a structured and appropriately challenging environment [4]. Therefore, youth must achieve sufficient technical mastery before advancing to more difficult and intense RT exercises [4]. More specifically, for youth with poor technical competency, the focus of a qualified practitioner should be on enhancing muscle strength while boosting their competence and confidence to perform various RT exercises [4]. On the other hand, technically competent youth can engage in more advanced RT exercises to optimize adaptations [4].
Conclusions and Future Research Endeavors
RT is a well-established training approach to improve muscular fitness in youth. Of note, cumulative evidence indicates that the benefits of RT can also cover those traditionally attributed to aerobic training in youth. More specifically, there is evidence that RT improves cardiorespiratory fitness, decreases body fat, and increases insulin sensitivity, among others. Furthermore, in terms of bone health, there is persuasive evidence that RT, particularly plyometric training, yields substantial positive effects, whereas aerobic training may have a lesser or even neutral impact on BMD enhancement (e.g., swimming). Regarding mental health and cognition, while aerobic training has well-documented positive effects, preliminary evidence, albeit in obese youth, suggest that RT may offer even greater benefits. Moreover, it is well established that RT is a powerful means to decrease the risk and rate of injuries in youth. Overall, convincing evidence suggests that RT should not be considered secondary to aerobic training. Instead, it seems reasonable to consider RT as an essential (possibly even the most essential) aspect of PA in future national and international guidelines. While prioritizing RT, it is crucial to acknowledge the complementary benefits of combining RT with aerobic training. Given the severe detrimental effects of paediatric dynapenia, including the onset of functional limitations, physical inactivity, sedentary behaviour, and heightened susceptibility to various negative health outcomes, we contend that future guidelines should specifically emphasize RT.
Considering the relatively limited number of studies, future research should aim to directly compare the effects of RT and aerobic training on physical fitness and health in both unhealthy and, in particular, healthy youth. Additionally, to gain more comprehensive insights, there is a need to explore the effects of adhering solely to the current RT guidelines versus only to the current aerobic training recommendations on health and physical fitness in youth. Moreover, further studies are required to investigate the dose–response relationship of RT on physical fitness and health in youth. These research endeavours are crucial to provide better, more specific and detailed guidelines.
Author Contributions
HC prepared the first draft of the manuscript. RRC, JM, LS, OP, IS, YN, and MB critically reviewed the manuscript and approved the final version.
Funding
Open Access funding enabled and organized by Projekt DEAL.
Declarations
Conflicts of Interest
Helmi Chaabene, Rodrigo Ramirez-Campillo, Jason Moran, Lutz Schega, Olaf Prieske, Ingo Sandau, Yassine Negra, and Martin Behrens declare that they have no conflicts of interest relevant to the content of this review.
Footnotes
Consists of jumping, hopping and skipping exercises that involve eccentric actions of the muscle–tendon unit, immediately followed by concentric actions – a process known as the stretch–shortening cycle [15].
Defined as a set of attributes that people have or achieve that relates to the ability to perform physical activity. It is categorized it into health-related (e.g., cardiovascular endurance, muscular strength, flexibility, body composition) and skill-related components (e.g., agility, balance, coordination, power, reaction time, speed) [16].
An insufficient physical activity level to meet current physical activity recommendations [44].
Activity in which the body’s large muscles move in a rhythmic manner for a sustained period of time. Aerobic activity – also called endurance activity – improves cardiorespiratory fitness. Examples include walking, running, swimming, and bicycling [44].
Fundamental movement skills refer to locomotor (running, skipping and hopping), manipulative (catching, throwing, grasping and striking), and stabilization (balance, twisting and bracing) skills [47].
Refers to the nervous system's ability to coordinate muscle activation for movement, force production and control.
References
- 1.Myer GD, Faigenbaum AD, Ford KR, Best TM, Bergeron MF, Hewett TE. When to initiate integrative neuromuscular training to reduce sports-related injuries and enhance health in youth? Curr Sports Med Rep. 2011;10(3):155–66. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Pediatrics AA. Weight training and weight lifting: information for the pediatrician. Phys Sportsmed. 1983;11(3):157–61. [DOI] [PubMed] [Google Scholar]
- 3.Kraemer WJ, Fry AC, Frykman PN, Conroy B, Hoffman J. Resistance training and youth. Pediatr Exerc Sci. 1989;1(4):336–50. [DOI] [PubMed] [Google Scholar]
- 4.Faigenbaum AD, Lloyd RS, MacDonald J, Myer GD. Citius, Altius, Fortius: beneficial effects of resistance training for young athletes: narrative review. Br J Sports Med. 2016;50(1):3–7. [DOI] [PubMed] [Google Scholar]
- 5.Faigenbaum AD, Kraemer WJ, Blimkie CJ, Jeffreys I, Micheli LJ, Nitka M, et al. Youth resistance training: updated position statement paper from the national strength and conditioning association. J Strength Cond Res. 2009;23(5 Suppl):S60-79. [DOI] [PubMed] [Google Scholar]
- 6.Faigenbaum AD, Myer GD. Resistance training among young athletes: safety, efficacy and injury prevention effects. Br J Sports Med. 2010;44(1):56–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Faigenbaum AD, Ratamess NA, Kang J, Bush JA, Rial RT. May the force be with youth: foundational strength for lifelong development. Curr Sports Med Rep. 2023;22(12):414–22. [DOI] [PubMed] [Google Scholar]
- 8.Phillips SM, Ma JK, Rawson ES. The coming of age of resistance exercise as a primary form of exercise for health. ACSM’s Health Fitness J. 2023;27(6):19–25. [Google Scholar]
- 9.Faigenbaum AD, MacDonald JP, Stracciolini A, Rebullido TR. Making a strong case for prioritizing muscular fitness in youth physical activity guidelines. Curr Sports Med Rep. 2020;19(12):530–6. [DOI] [PubMed] [Google Scholar]
- 10.Faigenbaum AD, Rebullido TR, Peña J, Chulvi-Medrano I. Resistance exercise for the prevention and treatment of pediatric dynapenia. J Sci Sport Exerc. 2019;1:208–16. [Google Scholar]
- 11.Tyler J, Thanos P. Raising the bar for public health: resistance training and health benefits. Int J Strength Cond. 2023;3(1).
- 12.Chaabene H, Lesinski M, Behm DG, Granacher U. Performance-and health-related benefits of youth resistance training. Sports Orthop Traumatol. 2020;36(3):231–40. [Google Scholar]
- 13.Lloyd RS, Oliver JL. The youth physical development model: a new approach to long-term athletic development. Strength Cond J. 2012;34(3):61–72. [Google Scholar]
- 14.Lloyd RS, Oliver JL, Faigenbaum AD, Howard R, Croix MBDS, Williams CA, et al. Long-term athletic development-part 1: a pathway for all youth. J Strength Cond Res. 2015;29(5):1439–50. [DOI] [PubMed] [Google Scholar]
- 15.Duchateau J, Amiridis IG. Plyometric exercises: optimizing the transfer of training gains to sport performance. Exerc Sport Sci Rev. 2023;51(4):117–27. [DOI] [PubMed] [Google Scholar]
- 16.Caspersen CJ, Powell KE, Christenson GM. Physical activity, exercise, and physical fitness: definitions and distinctions for health-related research. Public Health Reports (Washington, DC: 1974). 1985;100(2):126–31. [PMC free article] [PubMed] [Google Scholar]
- 17.Moran J, Sandercock G, Ramirez-Campillo R, Clark CCT, Fernandes JFT, Drury B. A meta-analysis of resistance training in female youth: its effect on muscular strength, and shortcomings in the literature. Sports Med (Auckland, NZ). 2018;48(7):1661–71. [DOI] [PubMed] [Google Scholar]
- 18.Moran J, Sandercock GR, Ramírez-Campillo R, Meylan C, Collison J, Parry DA. A meta-analysis of maturation-related variation in adolescent boy athletes’ adaptations to short-term resistance training. J Sports Sci. 2017;35(11):1041–51. [DOI] [PubMed] [Google Scholar]
- 19.Smith JJ, Eather N, Morgan PJ, Plotnikoff RC, Faigenbaum AD, Lubans DR. The health benefits of muscular fitness for children and adolescents: a systematic review and meta-analysis. Sports Med (Auckland, NZ). 2014;44(9):1209–23. [DOI] [PubMed] [Google Scholar]
- 20.Vicente-Rodríguez G. How does exercise affect bone development during growth? Sports Med (Auckland, NZ). 2006;36(7):561–9. [DOI] [PubMed] [Google Scholar]
- 21.Ishikawa S, Kim Y, Kang M, Morgan DW. Effects of weight-bearing exercise on bone health in girls: a meta-analysis. Sports Med (Auckland, NZ). 2013;43(9):875–92. [DOI] [PubMed] [Google Scholar]
- 22.Behringer M, Gruetzner S, McCourt M, Mester J. Effects of weight-bearing activities on bone mineral content and density in children and adolescents: a meta-analysis. J Bone Min Res. 2014;29(2):467–78. [DOI] [PubMed] [Google Scholar]
- 23.U.S. Department of Health and Human Services. (2018). Physical activity guidelines for Americans (2nd ed.). https://health.gov/sites/default/files/2019-09/Physical_Activity_Guidelines_2nd_edition.pdf. [DOI] [PubMed]
- 24.García-Hermoso A, Ramírez-Campillo R, Izquierdo M. Is muscular fitness associated with future health benefits in children and adolescents? A systematic review and meta-analysis of longitudinal studies. Sports Med. 2019;49:1079–94. [DOI] [PubMed] [Google Scholar]
- 25.Schranz N, Tomkinson G, Olds T. What is the effect of resistance training on the strength, body composition and psychosocial status of overweight and obese children and adolescents? A Systematic review and meta-analysis. Sports Med (Auckland, NZ). 2013;43(9):893–907. [DOI] [PubMed] [Google Scholar]
- 26.World Health Organisation (WHO). Physical activity. 2020. Nov 26, 2020; Available from: https://www.who.int/news-room/fact-sheets/detail/physical-activity.
- 27.Dias I, Farinatti P, de Souza MGC, Manhanini DP, Balthazar E, Dantas DLS, et al. Effects of resistance training on obese adolescents. Med Sci Sports Exerc. 2015;47(12):2636–44. [DOI] [PubMed] [Google Scholar]
- 28.Duarte Junior MA, Gaya AR, Mello JB, Faigenbaum AD, García-Hermoso A, López-Gil JF. Meeting muscle-strengthening recommendation is associated with lower adiposity, higher physical fitness and healthier lifestyle in adolescents: the EHDLA study. Acta Paediatr. 2024;113(5):1059–67. [DOI] [PubMed] [Google Scholar]
- 29.Robinson K, Riley N, Owen K, Drew R, Mavilidi MF, Hillman CH, et al. Effects of resistance training on academic outcomes in school-aged youth: a systematic review and meta-analysis. Sports Med (Auckland, NZ). 2023;53(11):2095–109. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.García-Hermoso A, López-Gil JF, Izquierdo M, Ramírez-Vélez R, Ezzatvar Y. Exercise and insulin resistance markers in children and adolescents with excess weight: a systematic review and network meta-analysis. JAMA Pediatr. 2023;177(12):1276–84. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Timpka S, Petersson IF, Zhou C, Englund M. Muscle strength in adolescent men and risk of cardiovascular disease events and mortality in middle age: a prospective cohort study. BMC Med. 2014;14(12):62. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Orsso CE, Tibaes JR, Oliveira CL, Rubin DA, Field CJ, Heymsfield SB, et al. Low muscle mass and strength in pediatrics patients: Why should we care? Clin Nutr. 2019;38(5):2002–15. [DOI] [PubMed] [Google Scholar]
- 33.Ortega FB, Silventoinen K, Tynelius P, Rasmussen F. Muscular strength in male adolescents and premature death: cohort study of one million participants. BMJ. 2012;345: e7279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Lesinski M, Herz M, Schmelcher A, Granacher U. Effects of resistance training on physical fitness in healthy children and adolescents: an umbrella review. Sports Med (Auckland, NZ). 2020;50(11):1901–28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Bright TE, Handford MJ, Mundy P, Lake J, Theis N, Hughes JD. Building for the future: a systematic review of the effects of eccentric resistance training on measures of physical performance in youth athletes. Sports Med (Auckland, NZ). 2023;53(6):1219–54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Schranz N, Tomkinson G, Parletta N, Petkov J, Olds T. Can resistance training change the strength, body composition and self-concept of overweight and obese adolescent males? A randomised controlled trial. Br J Sports Med. 2014;48(20):1482–8. [DOI] [PubMed] [Google Scholar]
- 37.Guthold R, Stevens GA, Riley LM, Bull FC. Global trends in insufficient physical activity among adolescents: a pooled analysis of 298 population-based surveys with 1.6 million participants. Lancet Child Adolescent Health. 2020;4(1):23–35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Hallal PC, Andersen LB, Bull FC, Guthold R, Haskell W, Ekelund U. Global physical activity levels: surveillance progress, pitfalls, and prospects. The Lancet. 2012;380(9838):247–57. [DOI] [PubMed] [Google Scholar]
- 39.Garcia-Hermoso A, López-Gil JF, Ramírez-Vélez R, Alonso-Martínez AM, Izquierdo M, Ezzatvar Y. Adherence to aerobic and muscle-strengthening activities guidelines: a systematic review and meta-analysis of 3.3 million participants across 32 countries. Br J Sports Med. 2023;57(4):225–9. [DOI] [PubMed] [Google Scholar]
- 40.Cheval B, Boisgontier MP. The theory of effort minimization in physical activity. Exerc Sport Sci Rev. 2021;49(3):168–78. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.García-Hermoso A, Izquierdo M, Ramírez-Vélez R. Tracking of physical fitness levels from childhood and adolescence to adulthood: a systematic review and meta-analysis. Transl Pediatrics. 2022;11(4):474–86. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Fraser BJ, Schmidt MD, Huynh QL, Dwyer T, Venn AJ, Magnussen CG. Tracking of muscular strength and power from youth to young adulthood: longitudinal findings from the Childhood Determinants of Adult Health Study. J Sci Med Sport. 2017;20(10):927–31. [DOI] [PubMed] [Google Scholar]
- 43.Boreham C, Riddoch C. The physical activity, fitness and health of children. J Sports Sci. 2001;19(12):915–29. [DOI] [PubMed] [Google Scholar]
- 44.Bull FC, Al-Ansari SS, Biddle S, Borodulin K, Buman MP, Cardon G, et al. World Health Organization 2020 guidelines on physical activity and sedentary behaviour. Br J Sports Med. 2020;54(24):1451–62. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Parrish AM, Tremblay MS, Carson S, Veldman SLC, Cliff D, Vella S, et al. Comparing and assessing physical activity guidelines for children and adolescents: a systematic literature review and analysis. Int J Behav Nutr Phys Activity. 2020;17(1):16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Duarte Junior MA, Gaya AR, Mello JB, Faigenbaum AD, García‐Hermoso A, López‐Gil JF. Meeting muscle‐strengthening recommendation is associated with lower adiposity, higher physical fitness and healthier lifestyle in adolescents: the EHDLA study. Acta Paediatrica. 2024. [DOI] [PubMed]
- 47.Lubans DR, Morgan PJ, Cliff DP, Barnett LM, Okely AD. Fundamental movement skills in children and adolescents: review of associated health benefits. Sports Med (Auckland, NZ). 2010;40(12):1019–35. [DOI] [PubMed] [Google Scholar]
- 48.Grøntved A, Ried-Larsen M, Ekelund U, Froberg K, Brage S, Andersen LB. Independent and combined association of muscle strength and cardiorespiratory fitness in youth with insulin resistance and β-cell function in young adulthood: the European Youth Heart Study. Diabetes Care. 2013;36(9):2575–81. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Lee S, Bacha F, Hannon T, Kuk JL, Boesch C, Arslanian S. Effects of aerobic versus resistance exercise without caloric restriction on abdominal fat, intrahepatic lipid, and insulin sensitivity in obese adolescent boys: a randomized, controlled trial. Diabetes. 2012;61(11):2787–95. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Hyde ET, Watson KB, Omura JD, Janz KF, Lee SM, Fulton JE, et al. Surveillance of meeting the youth physical activity guideline: impact of including vigorous-intensity and bone-strengthening activities. Res Q Exerc Sport. 2022;93(4):728–33. [DOI] [PubMed] [Google Scholar]
- 51.Services. USDoHaH. Physical activity guidelines for Americans (2nd ed.). 2018. https://health.gov/sites/default/files/2019-09/Physical_Activity_Guidelines_2nd_edition.pdf.
- 52.Eaton DK, Kann L, Kinchen S, Shanklin S, Flint KH, Hawkins J, et al. Youth risk behavior surveillance—United States, 2011. Morb Mortal Wkly Rep Recomm Rep. 2012;61(4):1–162. [PubMed] [Google Scholar]
- 53.Eaton DK, Kann L, Kinchen S, Shanklin S, Ross J, Hawkins J, et al. Youth risk behavior surveillance-United States, 2009. MMWR Surveill Summ. 2010;59(5):1–142. [PubMed] [Google Scholar]
- 54.Pereira S, Reyes AC, Chaves R, Santos C, Vasconcelos O, Tani G, et al. Correlates of the physical activity decline during childhood. Med Sci Sports Exerc. 2022;54(12):2129–37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Zwolski C, Quatman-Yates C, Paterno MV. Resistance training in youth: laying the foundation for injury prevention and physical literacy. Sports Health. 2017;9(5):436–43. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.De Meester A, Stodden D, Goodway J, True L, Brian A, Ferkel R, et al. Identifying a motor proficiency barrier for meeting physical activity guidelines in children. J Sci Med Sport. 2018;21(1):58–62. [DOI] [PubMed] [Google Scholar]
- 57.Faigenbaum AD, Lloyd RS, Myer GD. Youth resistance training: past practices, new perspectives, and future directions. Pediatr Exerc Sci. 2013;25(4):591–604. [DOI] [PubMed] [Google Scholar]
- 58.Goldfield GS, Kenny GP, Alberga AS, Prud’homme D, Hadjiyannakis S, Gougeon R, et al. Effects of aerobic training, resistance training, or both on psychological health in adolescents with obesity: the HEARTY randomized controlled trial. J Consult Clin Psychol. 2015;83(6):1123–35. [DOI] [PubMed] [Google Scholar]
- 59.Ekkekakis P, Lind E. Exercise does not feel the same when you are overweight: the impact of self-selected and imposed intensity on affect and exertion. Int J Obesity (2005). 2006;30(4):652–60. [DOI] [PubMed] [Google Scholar]
- 60.Brellenthin AG, Bennie JA, Lee DC. Aerobic or muscle-strengthening physical activity: which is better for health? Curr Sports Med Rep. 2022;21(8):272–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Faigenbaum AD, Bruno LE. A fundamental approach for treating pediatric dynapenia in kids. ACSM’s Health Fitness J. 2017;21(4):18–24. [Google Scholar]
- 62.Faigenbaum AD, MacDonald JP. Dynapenia: it’s not just for grown-ups anymore. Acta Paediatr. 2017;106(5):696–7. [DOI] [PubMed] [Google Scholar]
- 63.Li C, Taerken AY, Li Q, Selimu A, Wang H. Secular trends in physical fitness of rural Chinese children and adolescents aged 7–18 years from 1985 to 2019. Sci Rep. 2023;13(1):4229. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Wrotniak BH, Epstein LH, Dorn JM, Jones KE, Kondilis VA. The relationship between motor proficiency and physical activity in children. Pediatrics. 2006;118(6):e1758–65. [DOI] [PubMed] [Google Scholar]
- 65.Larsen LR, Kristensen PL, Junge T, Rexen CT, Wedderkopp N. Motor performance as predictor of physical activity in children: the CHAMPS study-DK. Med Sci Sports Exerc. 2015;47(9):1849–56. [DOI] [PubMed] [Google Scholar]
- 66.Shigaki GB, Batista MB, Paludo AC, Vignadelli LFZ, Serassuelo Junior H, Ronque ERV. Secular trend of physical fitness indicators related to health in children. J Hum Growth Dev. 2019;29(3):381–9. [Google Scholar]
- 67.Sandercock GR, Cohen DD. Temporal trends in muscular fitness of English 10-year-olds 1998–2014: an allometric approach. J Sci Med Sport. 2019;22(2):201–5. [DOI] [PubMed] [Google Scholar]
- 68.Gaya AR, Mello JB, Dias AF, Brand C, Cardoso VD, Nagorny GAK, et al. Temporal trends in physical fitness and obesity among Brazilian children and adolescents between 2008 and 2014. J Hum Sport Exerc Alicante. 2020;15(3):549–58. [Google Scholar]
- 69.Tomkinson GR, Kaster T, Dooley FL, Fitzgerald JS, Annandale M, Ferrar K, et al. Temporal trends in the standing broad jump performance of 10,940,801 children and adolescents between 1960 and 2017. Sports Med (Auckland, NZ). 2021;51(3):531–48. [DOI] [PubMed] [Google Scholar]
- 70.Kaster T, Dooley FL, Fitzgerald JS, Walch TJ, Annandale M, Ferrar K, et al. Temporal trends in the sit-ups performance of 9,939,289 children and adolescents between 1964 and 2017. J Sports Sci. 2020;38(16):1913–23. [DOI] [PubMed] [Google Scholar]
- 71.Dooley FL, Kaster T, Fitzgerald JS, Walch TJ, Annandale M, Ferrar K, et al. A systematic analysis of temporal trends in the handgrip strength of 2,216,320 children and adolescents between 1967 and 2017. Sports Med (Auckland, NZ). 2020;50(6):1129–44. [DOI] [PubMed] [Google Scholar]
- 72.Smith JJ, Eather N, Weaver RG, Riley N, Beets MW, Lubans DR. Behavioral correlates of muscular fitness in children and adolescents: a systematic review. Sports Med (Auckland, NZ). 2019;49(6):887–904. [DOI] [PubMed] [Google Scholar]
- 73.Fraser BJ, Blizzard L, Cleland V, Buscot MJ, Schmidt MD, Dwyer T, et al. Childhood factors associated with muscular strength trajectories between childhood and mid-adulthood. Med Sci Sports Exerc. 2022;54(11):1911–8. [DOI] [PubMed] [Google Scholar]
- 74.Rodríguez Valero FJ, Gualteros JA, Torres JA, Umbarila Espinosa LM, Ramírez-Velez R. Association between muscular fitness and physical health status among children and adolescents from Bogotá, Colombia. Nutr Hosp. 2015;32(4):1559–66. [DOI] [PubMed] [Google Scholar]
- 75.de Lima TR, Martins PC, Moreno YMF, Chaput JP, Tremblay MS, Sui X, et al. Muscular fitness and cardiometabolic variables in children and adolescents: a systematic review. Sports Med (Auckland, NZ). 2022;52(7):1555–75. [DOI] [PubMed] [Google Scholar]
- 76.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):1–11. [DOI] [PubMed] [Google Scholar]
- 77.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(12):909–23. [DOI] [PubMed] [Google Scholar]
- 78.Holtebekk ME, Berntsen S, Rasmussen M, Jahnsen RB. Physical activity and motor function in children and adolescents with neuromuscular disorders. Pediatr Phys Ther. 2013;25(4):415–20. [DOI] [PubMed] [Google Scholar]
- 79.Maher CA, Williams MT, Olds T, Lane AE. Physical and sedentary activity in adolescents with cerebral palsy. Dev Med Child Neurol. 2007;49(6):450–7. [DOI] [PubMed] [Google Scholar]
- 80.Lelieveld OT, Armbrust W, van Leeuwen MA, Duppen N, Geertzen JH, Sauer PJ, et al. Physical activity in adolescents with juvenile idiopathic arthritis. Arthritis Rheum. 2008;59(10):1379–84. [DOI] [PubMed] [Google Scholar]
- 81.Epstein LH, Valoski AM, Vara LS, McCurley J, Wisniewski L, Kalarchian MA, et al. Effects of decreasing sedentary behavior and increasing activity on weight change in obese children. Health Psychol. 1995;14(2):109. [DOI] [PubMed] [Google Scholar]
- 82.Castro-Piñero J, Perez-Bey A, Cuenca-Garcia M, Cabanas-Sanchez V, Gómez-Martínez S, Veiga OL, et al. Muscle fitness cut points for early assessment of cardiovascular risk in children and adolescents. J Pediatr. 2019;206(134–41): e3. [DOI] [PubMed] [Google Scholar]
- 83.Martínez-Gómez D, Welk GJ, Puertollano M, Del-Campo J, Moya J, Marcos A, et al. Associations of physical activity with muscular fitness in adolescents. Scand J Med Sci Sports. 2011;21(2):310–7. [DOI] [PubMed] [Google Scholar]
- 84.Henriksson H, Henriksson P, Tynelius P, Ortega FB. Muscular weakness in adolescence is associated with disability 30 years later: a population-based cohort study of 1.2 million men. Br J Sports Med. 2019;53(19):1221–30. [DOI] [PubMed] [Google Scholar]
- 85.Telama R, Yang X, Leskinen E, Kankaanpää A, Hirvensalo M, Tammelin T, et al. Tracking of physical activity from early childhood through youth into adulthood. Med Sci Sports Exerc. 2014;46(5):955–62. [DOI] [PubMed] [Google Scholar]
- 86.Telama R, Yang X, Viikari J, Välimäki I, Wanne O, Raitakari O. Physical activity from childhood to adulthood: a 21-year tracking study. Am J Prev Med. 2005;28(3):267–73. [DOI] [PubMed] [Google Scholar]
- 87.Huotari P, Nupponen H, Mikkelsson L, Laakso L, Kujala U. Adolescent physical fitness and activity as predictors of adulthood activity. J Sports Sci. 2011;29(11):1135–41. [DOI] [PubMed] [Google Scholar]
- 88.Telama R. Tracking of physical activity from childhood to adulthood: a review. Obes Facts. 2009;2(3):187–95. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Fraser BJ, Blizzard L, Buscot MJ, Schmidt MD, Dwyer T, Venn AJ, et al. Muscular strength across the life course: the tracking and trajectory patterns of muscular strength between childhood and mid-adulthood in an Australian cohort. J Sci Med Sport. 2021;24(7):696–701. [DOI] [PubMed] [Google Scholar]
- 90.Thompson AM, Humbert ML, Mirwald RL. A longitudinal study of the impact of childhood and adolescent physical activity experiences on adult physical activity perceptions and behaviors. Qual Health Res. 2003;13(3):358–77. [DOI] [PubMed] [Google Scholar]
- 91.Faigenbaum AD, Myer GD. Pediatric resistance training: benefits, concerns, and program design considerations. Curr Sports Med Rep. 2010;9(3):161–8. [DOI] [PubMed] [Google Scholar]
- 92.Faigenbaum AD, Stracciolini A, MacDonald JP, Rebullido TR. Mythology of youth resistance training. Br J Sports Med. 2022. 10.1136/bjsports-2022-105804. [DOI] [PubMed] [Google Scholar]
- 93.Stricker PR, Faigenbaum AD, McCambridge TM, LaBella CR, Brooks MA, Canty G, et al. Resistance training for children and adolescents. Pediatrics. 2020. 10.1542/peds.2020-1011. [DOI] [PubMed] [Google Scholar]
- 94.Lloyd RS, Faigenbaum AD, Stone MH, Oliver JL, Jeffreys I, Moody JA, et al. Position statement on youth resistance training: the 2014 International Consensus. Br J Sports Med. 2014;48(7):498–505. [DOI] [PubMed] [Google Scholar]
- 95.Goldfield GS, Kenny GP, Alberga AS, Tulloch HE, Doucette S, Cameron JD, et al. Effects of aerobic or resistance training or both on health-related quality of life in youth with obesity: the HEARTY Trial. Appl Physiol Nutr Metab = Physiologie appliquee, nutrition et metabolisme. 2017;42(4):361–70. [DOI] [PubMed] [Google Scholar]
- 96.Lee S, Deldin AR, White D, Kim Y, Libman I, Rivera-Vega M, et al. Aerobic exercise but not resistance exercise reduces intrahepatic lipid content and visceral fat and improves insulin sensitivity in obese adolescent girls: a randomized controlled trial. Am J Physiol-Endocrinol Metab. 2013;305(10):E1222–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 97.Marson EC, Delevatti RS, Prado AK, Netto N, Kruel LF. Effects of aerobic, resistance, and combined exercise training on insulin resistance markers in overweight or obese children and adolescents: a systematic review and meta-analysis. Prev Med. 2016;93:211–8. [DOI] [PubMed] [Google Scholar]
- 98.Sigal RJ, Alberga AS, Goldfield GS, Prud’homme D, Hadjiyannakis S, Gougeon R, et al. Effects of aerobic training, resistance training, or both on percentage body fat and cardiometabolic risk markers in obese adolescents: the healthy eating aerobic and resistance training in youth randomized clinical trial. JAMA Pediatr. 2014;168(11):1006–14. [DOI] [PubMed] [Google Scholar]
- 99.Lee S, Libman I, Hughan K, Kuk JL, Jeong JH, Zhang D, et al. Effects of exercise modality on insulin resistance and ectopic fat in adolescents with overweight and obesity: a randomized clinical trial. J Pediatr. 2019;206(91–8): e1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 100.Inoue DS, De Mello MT, Foschini D, Lira FS, Ganen ADP, Campos RMDS, et al. Linear and undulating periodized strength plus aerobic training promote similar benefits and lead to improvement of insulin resistance on obese adolescents. J Diabetes Complicat. 2015;29(2):258–64. [DOI] [PubMed] [Google Scholar]
- 101.Dâmaso AR, da Silveira Campos RM, Caranti DA, de Piano A, Fisberg M, Foschini D, et al. Aerobic plus resistance training was more effective in improving the visceral adiposity, metabolic profile and inflammatory markers than aerobic training in obese adolescents. J Sports Sci. 2014;32(15):1435–45. [DOI] [PubMed] [Google Scholar]
- 102.Lee S, Kim Y, Kuk JL. What is the role of resistance exercise in improving the cardiometabolic health of adolescents with obesity? J Obesity Metab Syndrome. 2019;28(2):76. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 103.Åberg ND, Kuhn HG, Nyberg J, Waern M, Friberg P, Svensson J, et al. Influence of cardiovascular fitness and muscle strength in early adulthood on long-term risk of stroke in Swedish men. Stroke. 2015;46(7):1769–76. [DOI] [PubMed] [Google Scholar]
- 104.Peterson MD, Zhang P, Saltarelli WA, Visich PS, Gordon PM. Low muscle strength thresholds for the detection of cardiometabolic risk in adolescents. Am J Prev Med. 2016;50(5):593–9. [DOI] [PubMed] [Google Scholar]
- 105.Artero EG, Ruiz JR, Ortega FB, España-Romero V, Vicente-Rodríguez G, Molnar D, et al. Muscular and cardiorespiratory fitness are independently associated with metabolic risk in adolescents: the HELENA study. Pediatr Diabetes. 2011;12(8):704–12. [DOI] [PubMed] [Google Scholar]
- 106.Peterson MD, Saltarelli WA, Visich PS, Gordon PM. Strength capacity and cardiometabolic risk clustering in adolescents. Pediatrics. 2014;133(4):e896–903. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 107.Cohen DD, Gómez-Arbeláez D, Camacho PA, Pinzon S, Hormiga C, Trejos-Suarez J, et al. Low muscle strength is associated with metabolic risk factors in Colombian children: the ACFIES study. PLoS One. 2014;9(4): e93150. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 108.Stovitz SD, Verhagen E, Shrier I. Distinguishing between causal and non-causal associations: implications for sports medicine clinicians. BMJ Publishing Group Ltd and British Association of Sport and Exercise Medicine; 2019. pp. 398–9. [DOI] [PubMed]
- 109.Kim S, Valdez R. Metabolic risk factors in US youth with low relative muscle mass. Obes Res Clin Pract. 2015;9(2):125–32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110.Kim J-H, Park YS. Low muscle mass is associated with metabolic syndrome in Korean adolescents: the Korea National Health and Nutrition Examination Survey 2009–2011. Nutr Res. 2016;36(12):1423–8. [DOI] [PubMed] [Google Scholar]
- 111.Blakeley CE, Van Rompay MI, Schultz NS, Sacheck JM. Relationship between muscle strength and dyslipidemia, serum 25 (OH) D, and weight status among diverse schoolchildren: a cross-sectional analysis. BMC Pediatr. 2018;18:1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 112.Gomes TN, Dos Santos FK, Katzmarzyk PT, Maia J. Active and strong: physical activity, muscular strength, and metabolic risk in children. Am J Hum Biol. 2017. 10.1002/ajhb.22904. [DOI] [PubMed] [Google Scholar]
- 113.Steene-Johannessen J, Anderssen SA, Kolle E, Andersen LB. Low muscle fitness is associated with metabolic risk in youth. Med Sci Sports Exerc. 2009;41(7):1361–7. [DOI] [PubMed] [Google Scholar]
- 114.Proia P, Amato A, Drid P, Korovljev D, Vasto S, Baldassano S. The impact of diet and physical activity on bone health in children and adolescents. Front Endocrinol. 2021;12: 704647. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 115.Min SK, Oh T, Kim SH, Cho J, Chung HY, Park DH, et al. Position statement: exercise guidelines to increase peak bone mass in adolescents. J Bone Metab. 2019;26(4):225–39. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 116.Gordon RJ, Gordon CM. Adolescents and bone health. Clin Obstet Gynecol. 2020;63(3):504–11. [DOI] [PubMed] [Google Scholar]
- 117.McCormack SE, Cousminer DL, Chesi A, Mitchell JA, Roy SM, Kalkwarf HJ, et al. Association between linear growth and bone accrual in a diverse cohort of children and adolescents. JAMA Pediatr. 2017;171(9): e171769. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 118.Bloomfield SA, Little K, Nelson M, Yingling V. American College of Sports Medicine position stand: physical activity and bone health. Med Sci Sports Exerc. 2004;195(9131/04):3611. [DOI] [PubMed] [Google Scholar]
- 119.Heaney RP, Abrams S, Dawson-Hughes B, Looker A, Marcus R, Matkovic V, et al. Peak bone mass. Osteoporosis Int. 2000;11(12):985. [DOI] [PubMed] [Google Scholar]
- 120.Hernandez C, Beaupre G, Carter D. A theoretical analysis of the relative influences of peak BMD, age-related bone loss and menopause on the development of osteoporosis. Osteoporos Int. 2003;14:843–7. [DOI] [PubMed] [Google Scholar]
- 121.Clark EM, Ness AR, Bishop NJ, Tobias JH. Association between bone mass and fractures in children: a prospective cohort study. J Bone Miner Res. 2006;21(9):1489–95. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 122.Baxter-Jones AD, Kontulainen SA, Faulkner RA, Bailey DA. A longitudinal study of the relationship of physical activity to bone mineral accrual from adolescence to young adulthood. Bone. 2008;43(6):1101–7. [DOI] [PubMed] [Google Scholar]
- 123.Cooper C, Cole ZA, Holroyd CR, Earl SC, Harvey NC, Dennison EM, et al. Secular trends in the incidence of hip and other osteoporotic fractures. Osteop Int. 2011;22(5):1277–88. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 124.Rizzoli R, Bianchi ML, Garabédian M, McKay HA, Moreno LA. Maximizing bone mineral mass gain during growth for the prevention of fractures in the adolescents and the elderly. Bone. 2010;46(2):294–305. [DOI] [PubMed] [Google Scholar]
- 125.Sioen I, Lust E, De Henauw S, Moreno L, Jiménez-Pavón D. Associations between body composition and bone health in children and adolescents: a systematic review. Calcif Tissue Int. 2016;99:557–77. [DOI] [PubMed] [Google Scholar]
- 126.Chan D, Lee W, Lo D, Leung J, Kwok A, Leung P. Relationship between grip strength and bone mineral density in healthy Hong Kong adolescents. Osteoporos Int. 2008;19:1485–95. [DOI] [PubMed] [Google Scholar]
- 127.Tsuji S, Tsunoda N, Yata H, Katsukawa F, Onishi S, Yamazaki H. Relation between grip strength and radial bone mineral density in young athletes. Arch Phys Med Rehabil. 1995;76(3):234–8. [DOI] [PubMed] [Google Scholar]
- 128.Kristinsson J, Valdimarsson Ö, Steingrimsdottir L, Sigurdsson G. Relation between calcium intake, grip strength and bone mineral density in the forearms of girls aged 13 and 15. J Intern Med. 1994;236(4):385–90. [DOI] [PubMed] [Google Scholar]
- 129.Pillsbury L, Oria M, Pate R. Fitness measures and health outcomes in youth. 2013. [PubMed]
- 130.Saint-Maurice PF, Laurson K, Welk GJ, Eisenmann J, Gracia-Marco L, Artero EG, et al. Grip strength cutpoints for youth based on a clinically relevant bone health outcome. Arch Osteoporos. 2018;13:1–9. [DOI] [PubMed] [Google Scholar]
- 131.Weeks BK, Young CM, Beck BR. Eight months of regular in-school jumping improves indices of bone strength in adolescent boys and girls: the POWER PE study. J Bone Miner Res. 2008;23(7):1002–11. [DOI] [PubMed] [Google Scholar]
- 132.Vlachopoulos D, Barker AR, Ubago-Guisado E, Williams CA, Gracia-Marco L. A 9-month jumping intervention to improve bone geometry in adolescent male athletes. 2018. [DOI] [PubMed]
- 133.MacKelvie K, McKay H, Petit M, Moran O, Khan K. Bone mineral response to a 7-month randomized controlled, school-based jumping intervention in 121 prepubertal boys: associations with ethnicity and body mass index. J Bone Miner Res. 2002;17(5):834–44. [DOI] [PubMed] [Google Scholar]
- 134.Larsen MN, Nielsen CM, Helge EW, Madsen M, Manniche V, Hansen L, et al. Positive effects on bone mineralisation and muscular fitness after 10 months of intense school-based physical training for children aged 8–10 years: the FIT FIRST randomised controlled trial. Br J Sports Med. 2018;52(4):254–60. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 135.Witzke KA, Snow CM. Effects of polymetric jump training on bone mass in adolescent girls. Med Sci Sports Exerc. 2000;32(6):1051–7. [DOI] [PubMed] [Google Scholar]
- 136.Kontulainen S, Kannus P, Pasanen M, Sievänen H, Heinonen A, Oja P, et al. Does previous participation in high-impact training result in residual bone gain in growing girls? Int J Sports Med. 2002;23(08):575–81. [DOI] [PubMed] [Google Scholar]
- 137.Gunter KB, Almstedt HC, Janz KF. Physical activity in childhood may be the key to optimizing lifespan skeletal health. Exerc Sport Sci Rev. 2012;40(1):13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 138.Nguyen VH. School-based exercise interventions effectively increase bone mineralization in children and adolescents. Osteoporosis Sarcopenia. 2018;4(2):39–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 139.Gómez-Bruton A, Matute-Llorente Á, González-Agüero A, Casajus JA, Vicente-Rodríguez G. Plyometric exercise and bone health in children and adolescents: a systematic review. World J Pediatrics. 2017;13:112–21. [DOI] [PubMed] [Google Scholar]
- 140.Eliakim A, Raisz LG, Brasel JA, Cooper DM. Evidence for increased bone formation following a brief endurance-type training intervention in adolescent males. J Bone Miner Res. 1997;12(10):1708–13. [DOI] [PubMed] [Google Scholar]
- 141.Tian X, Fu J, Tian J, Yang Y, Liang W, Fan W, et al. The efficacy of brief school-based exercise programs in improving pubertal bone mass and physical fitness: a randomized controlled trial. Int J Environ Res Public Health. 2021;18(18):9648. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 142.Heinonen A, Oja P, Kannus P, Sievänen H, Mänttäri A, Vuori I. Bone mineral density of female athletes in different sports. Bone Miner. 1993;23(1):1–14. [DOI] [PubMed] [Google Scholar]
- 143.Choi H, Lee C, Kang H. Bone mineral density in different types of sports: Female high school athletes. J Korean Phys Educ Assoc Girls Women. 2006;20:37–44. [Google Scholar]
- 144.Agostinete RR, Maillane-Vanegas S, Lynch KR, Turi-Lynch B, Coelho-e-Silva MJ, Campos EZ, et al. The impact of training load on bone mineral density of adolescent swimmers: a structural equation modeling approach. Pediatr Exerc Sci. 2017;29(4):520–8. [DOI] [PubMed] [Google Scholar]
- 145.Bellew JW, Gehrig L. A comparison of bone mineral density in adolescent female swimmers, soccer players, and weight lifters. Pediatr Phys Ther. 2006;18(1):19–22. [DOI] [PubMed] [Google Scholar]
- 146.Ribeiro-Dos-Santos MR, Lynch KR, Agostinete RR, Maillane-Vanegas S, Turi-Lynch B, Ito IH, et al. Prolonged practice of swimming is negatively related to bone mineral density gains in adolescents. J Bone Metab. 2016;23(3):149–55. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 147.Burrows M, Nevill AM, Bird S, Simpson D. Physiological factors associated with low bone mineral density in female endurance runners. Br J Sports Med. 2003;37(1):67–71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 148.Burns RD, Kim Y, Fu Y, Byun W, Bai Y. Independent and joint associations of aerobic and muscle-strengthening exercise with mental health in adolescents: a cross-sectional analysis before and during COVID-19 using the 2015–2021 National Youth Risk Behavior Survey. Prev Med. 2023;177: 107750. [DOI] [PubMed] [Google Scholar]
- 149.Chiang H-L, Chuang Y-F, Chen Y-A, Hsu C-T, Ho C-C, Hsu H-T, et al. Physical fitness and risk of mental disorders in children and adolescents. JAMA Pediatr. 2024;178(6):595. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 150.Eather N, Morgan PJ, Lubans DR. Effects of exercise on mental health outcomes in adolescents: Findings from the CrossFit™ teens randomized controlled trial. Psychol Sport Exerc. 2016;26:14–23. [Google Scholar]
- 151.Collins H, Booth JN, Duncan A, Fawkner S, Niven A. The effect of resistance training interventions on ‘the self’in youth: a systematic review and meta-analysis. Sports medicine-open. 2019;5(1):1–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 152.Tomporowski PD, Pesce C. Exercise, sports, and performance arts benefit cognition via a common process. Psychol Bull. 2019;145(9):929. [DOI] [PubMed] [Google Scholar]
- 153.Jaworska N, Courtright AK, De Somma E, MacQueen GM, MacMaster FP. Aerobic exercise in depressed youth: a feasibility and clinical outcomes pilot. Early Interv Psychiatry. 2019;13(1):128–32. [DOI] [PubMed] [Google Scholar]
- 154.Leahy AA, Mavilidi MF, Smith JJ, Hillman CH, Eather N, Barker D, et al. Review of high-intensity interval training for cognitive and mental health in youth. Med Sci Sports Exerc. 2020;52(10):2224–34. [DOI] [PubMed] [Google Scholar]
- 155.Costigan SA, Eather N, Plotnikoff RC, Hillman CH, Lubans DR. High-intensity interval training for cognitive and mental health in adolescents. Med Sci Sports Exerc. 2016;48(10):1985–93. [DOI] [PubMed] [Google Scholar]
- 156.Alves AR, Dias R, Neiva HP, Marinho DA, Marques MC, Sousa AC, et al. High-intensity interval training upon cognitive and psychological outcomes in youth: a systematic review. Int J Environ Res Public Health. 2021;18(10):5344. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 157.Walters BK, Read CR, Estes AR. The effects of resistance training, overtraining, and early specialization on youth athlete injury and development. J Sports Med Phys Fitness. 2018;58(9):1339–48. [DOI] [PubMed] [Google Scholar]
- 158.Sugimoto D, Myer GD, Foss KD, Hewett TE. Specific exercise effects of preventive neuromuscular training intervention on anterior cruciate ligament injury risk reduction in young females: meta-analysis and subgroup analysis. Br J Sports Med. 2015;49(5):282–9. [DOI] [PubMed] [Google Scholar]
- 159.Collard DC, Verhagen EA, Chinapaw MJ, Knol DL, Van Mechelen W. Effectiveness of a school-based physical activity injury prevention program: a cluster randomized controlled trial. Arch Pediatr Adolesc Med. 2010;164(2):145–50. [DOI] [PubMed] [Google Scholar]
- 160.Myer GD, Faigenbaum AD, Chu DA, Falkel J, Ford KR, Best TM, et al. Integrative training for children and adolescents: techniques and practices for reducing sports-related injuries and enhancing athletic performance. Phys Sportsmed. 2011;39(1):74–84. [DOI] [PubMed] [Google Scholar]
- 161.Valovich McLeod TC, Decoster LC, Loud KJ, Micheli LJ, Parker JT, Sandrey MA, et al. National Athletic Trainers’ Association position statement: prevention of pediatric overuse injuries. J Athl Train. 2011;46(2):206–20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 162.Torres Martín L, Raya-González J, Ramirez-Campillo R, Chaabene H, Sánchez-Sánchez J. Effects of body mass-based resistance training on measures of physical fitness and musculotendinous injury incidence and burden in U16 male soccer players. Res Sports Med (Print). 2023;31(5):574–87. [DOI] [PubMed] [Google Scholar]
- 163.Emery CA, Roy T-O, Whittaker JL, Nettel-Aguirre A, Van Mechelen W. Neuromuscular training injury prevention strategies in youth sport: a systematic review and meta-analysis. Br J Sports Med. 2015;49(13):865–70. [DOI] [PubMed] [Google Scholar]
- 164.Abernethy L, Bleakley C. Strategies to prevent injury in adolescent sport: a systematic review. Br J Sports Med. 2007;41(10):627–38. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 165.Lauersen JB, Bertelsen DM, Andersen LB. The effectiveness of exercise interventions to prevent sports injuries: a systematic review and meta-analysis of randomised controlled trials. Br J Sports Med. 2014;48(11):871–7. [DOI] [PubMed] [Google Scholar]
- 166.Rössler R, Donath L, Verhagen E, Junge A, Schweizer T, Faude O. Exercise-based injury prevention in child and adolescent sport: a systematic review and meta-analysis. Sports Med. 2014;44:1733–48. [DOI] [PubMed] [Google Scholar]
- 167.Emery CA, Owoeye OBA, Räisänen AM, Befus K, Hubkarao T, Palacios-Derflingher L, et al. The “SHRed Injuries Basketball” neuromuscular training warm-up program reduces ankle and knee injury rates by 36% in youth basketball. J Orthop Sports Phys Ther. 2022;52(1):40–8. [DOI] [PubMed] [Google Scholar]
- 168.Steib S, Rahlf AL, Pfeifer K, Zech A. Dose-response relationship of neuromuscular training for injury prevention in youth athletes: a meta-analysis. Front Physiol. 2017;8: 304579. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 169.Frisch A, Croisier J-L, Urhausen A, Seil R, Theisen D. Injuries, risk factors and prevention initiatives in youth sport. Br Med Bull. 2009;92(1):95–121. [DOI] [PubMed] [Google Scholar]
- 170.Emery CA. Risk factors for injury in child and adolescent sport: a systematic review of the literature. Clin J Sport Med. 2003;13(4):256–68. [DOI] [PubMed] [Google Scholar]
- 171.Mandorino M, Figueiredo AJ, Gjaka M, Tessitore A. Injury incidence and risk factors in youth soccer players: a systematic literature review. Part II: Intrinsic and extrinsic risk factors. Biol Sport. 2023;40(1):27–49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 172.Sammoud S, Negra Y, Bouguezzi R, Ramirez-Campillo R, Moran J, Bishop C, et al. Effects of plyometric jump training on measures of physical fitness and lower-limb asymmetries in prepubertal male soccer players: a randomized controlled trial. BMC Sports Sci Med Rehabil. 2024;16(1):37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 173.Legerlotz K, Marzilger R, Bohm S, Arampatzis A. Physiological adaptations following resistance training in youth athletes-a narrative review. Pediatr Exerc Sci. 2016;28(4):501–20. [DOI] [PubMed] [Google Scholar]
- 174.McQuilliam SJ, Clark DR, Erskine RM, Brownlee TE. Free-weight resistance training in youth athletes: a narrative review. Sports Med (Auckland, NZ). 2020;50(9):1567–80. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 175.Suchomel TJ, Nimphius S, Bellon CR, Stone MH. The importance of muscular strength: training considerations. Sports Med (Auckland, NZ). 2018;48(4):765–85. [DOI] [PubMed] [Google Scholar]
- 176.Behm DG, Faigenbaum AD, Falk B, Klentrou P. Canadian Society for Exercise Physiology position paper: resistance training in children and adolescents. Appl Physiol Nutr Metab = Physiologie appliquee, nutrition et metabolisme. 2008;33(3):547–61. [DOI] [PubMed] [Google Scholar]
- 177.Malina RM, Bouchard C, & Bar-Or O. Growth, maturation, and physical activity: Human kinetics; 2004.
- 178.Gralla MH, McDonald SM, Breneman C, Beets MW, Moore JB. Associations of objectively measured vigorous physical activity with body composition, cardiorespiratory fitness, and cardiometabolic health in youth: a review. Am J Lifestyle Med. 2019;13(1):61–97. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 179.Hussey J, Bell C, Bennett K, O’dwyer J, Gormley J. Relationship between the intensity of physical activity, inactivity, cardiorespiratory fitness and body composition in 7–10-year-old Dublin children. Br J Sports Med. 2007;41(5):311–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 180.Alberga AS, Prud’homme D, Sigal RJ, Goldfield GS, Hadjiyannakis S, Phillips P, et al. Effects of aerobic training, resistance training, or both on cardiorespiratory and musculoskeletal fitness in adolescents with obesity: the HEARTY trial. Appl Physiol Nutr Metab. 2016;41(3):255–65. [DOI] [PubMed] [Google Scholar]
- 181.Konopka AR, Harber MP. Skeletal muscle hypertrophy after aerobic exercise training. Exerc Sport Sci Rev. 2014;42(2):53–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 182.Harber MP, Konopka AR, Undem MK, Hinkley JM, Minchev K, Kaminsky LA, et al. Aerobic exercise training induces skeletal muscle hypertrophy and age-dependent adaptations in myofiber function in young and older men. J Appl Physiol (Bethesda, Md: 2985). 2012;113(9):1495–504. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 183.Sammoud S, Negra Y, Chaabene H, Bouguezzi R, Moran J, Granacher U. The effects of plyometric jump training on jumping and swimming performances in prepubertal male swimmers. J Sports Sci Med. 2019;18(4):805–11. [PMC free article] [PubMed] [Google Scholar]
- 184.Bouguezzi R, Chaabene H, Negra Y, Ramirez-Campillo R, Jlalia Z, Mkaouer B, et al. Effects of different plyometric training frequencies on measures of athletic performance in prepuberal male soccer players. J Strength Cond Res. 2020;34(6):1609–17. [DOI] [PubMed] [Google Scholar]
- 185.Chaabene H, Negra Y, Moran J, Prieske O, Sammoud S, Ramirez-Campillo R, et al. Plyometric training improves not only measures of linear speed, power, and change-of-direction speed but also repeated sprint ability in young female handball players. J Strength Cond Res. 2021;35(8):2230–5. [DOI] [PubMed] [Google Scholar]
- 186.Sammoud S, Bouguezzi R, Ramirez-Campillo R, Negra Y, Prieske O, Moran J, et al. Effects of plyometric jump training versus power training using free weights on measures of physical fitness in youth male soccer players. J Sports Sci. 2022;40(2):130–7. [DOI] [PubMed] [Google Scholar]
- 187.Negra Y, Chaabene H, Stöggl T, Hammami M, Chelly MS, Hachana Y. Effectiveness and time-course adaptation of resistance training vs. plyometric training in prepubertal soccer players. J Sport Health Sci. 2020;9(6):620–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 188.Chaabene H, Negra Y, Moran J, Prieske O, Sammoud S, Ramirez-Campillo R, et al. Effects of an eccentric hamstrings training on components of physical performance in young female handball players. Int J Sports Physiol Perform. 2020;15(1):91–7. [DOI] [PubMed] [Google Scholar]
- 189.Chaabene H, Negra Y, Sammoud S, Moran J, Ramirez-Campillo R, Granacher U, et al. The effects of combined balance and complex training versus complex training only on measures of physical fitness in young female handball players. Int J Sports Physiol Perform. 2021;16(10):1439–46. [DOI] [PubMed] [Google Scholar]
- 190.Negra Y, Chaabene H, Sammoud S, Prieske O, Moran J, Ramirez-Campillo R, et al. The increased effectiveness of loaded versus unloaded plyometric jump training in improving muscle power, speed, change of direction, and kicking-distance performance in prepubertal male soccer players. Int J Sports Physiol Perform. 2020;15(2):189–95. [DOI] [PubMed] [Google Scholar]
- 191.Negra Y, Chaabene H, Hammami M, Hachana Y, Granacher U. Effects of high-velocity resistance training on athletic performance in prepuberal male soccer athletes. J Strength Cond Res. 2016;30(12):3290–7. [DOI] [PubMed] [Google Scholar]
- 192.Granacher U, Goesele A, Roggo K, Wischer T, Fischer S, Zuerny C, et al. Effects and mechanisms of strength training in children. Int J Sports Med. 2011:357–64. [DOI] [PubMed]
- 193.Assunção AR, Bottaro M, Ferreira-Junior JB, Izquierdo M, Cadore EL, Gentil P. The chronic effects of low-and high-intensity resistance training on muscular fitness in adolescents. PLoS One. 2016;11(8): e0160650. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 194.Faigenbaum AD, Milliken LA, Loud RL, Burak BT, Doherty CL, Westcott WL. Comparison of 1 and 2 days per week of strength training in children. Res Q Exerc Sport. 2002;73(4):416–24. [DOI] [PubMed] [Google Scholar]
- 195.Lillegard WA, Brown EW, Wilson DJ, Henderson R, Lewis E. Efficacy of strength training in prepubescent to early postpubescent males and females: effects of gender and maturity. Pediatr Rehabil. 1997;1(3):147–57. [DOI] [PubMed] [Google Scholar]
- 196.Sadres E, Eliakim A, Constantini N, Lidor R, Falk B. The effect of long-term resistance training on anthropometric measures, muscle strength, and self concept in pre-pubertal boys. Pediatr Exerc Sci. 2001;13(4):357–72. [Google Scholar]
- 197.Lesinski M, Prieske O, Granacher U. Effects and dose-response relationships of resistance training on physical performance in youth athletes: a systematic review and meta-analysis. Br J Sports Med. 2016;50(13):781–95. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 198.Stratton G, Jones M, Fox K, Tolfrey K, Harris J, Maffulli N, et al. BASES position statement on guidelines for resistance exercise in young people. J Sports Sci. 2004;22(4):383–90. [DOI] [PubMed] [Google Scholar]
- 199.Tøien T, Nielsen JL, Berg OK, Brobakken MF, Nyberg SK, Espedal L, et al. The impact of life-long strength versus endurance training on muscle fiber morphology and phenotype composition in older men. J Appl Physiol (Bethesda, Md: 1985). 2023;135(6):1360–71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 200.de Salles Painelli V. Risks and recommendations for resistance training in youth athletes: a narrative review with emphasis on muscular fitness and hypertrophic responses. J Sci Sport Exerc. 2023. 10.1007/s42978-023-00251-y. [Google Scholar]
- 201.Fukunaga T, Funato K. The effects of resistance training on muscle area and strength in prepubescent age. Ann Physiol Anthropol. 1992;11(3):357–64. [DOI] [PubMed] [Google Scholar]
- 202.Ramsay JA, Blimkie C, Smith K, Garner S, MacDougall JD, Sale DG. Strength training effects in prepubescent boys. Med Sci Sports Exerc. 1990;22(5):605–14. [DOI] [PubMed] [Google Scholar]
- 203.Vrijens J. Muscle strength development in the pre-and post-pubescent age. Pediatric work physiology. Karger Publishers; 1978. p. 152–8. [Google Scholar]
- 204.Guy JA, Micheli LJ. Strength training for children and adolescents. JAAOS-J Am Acad Orthop Surgeons. 2001;9(1):29–36. [DOI] [PubMed] [Google Scholar]
- 205.Malina RM. Weight training in youth-growth, maturation, and safety: an evidence-based review. Clin J Sport Med. 2006;16(6):478–87. [DOI] [PubMed] [Google Scholar]
- 206.Ozmun JC, Mikesky AE, Surburg PR. Neuromuscular adaptations following prepubescent strength training. Med Sci Sports Exerc. 1994;26(4):510–4. [PubMed] [Google Scholar]
- 207.Vingren JL, Kraemer WJ, Ratamess NA, Anderson JM, Volek JS, Maresh CM. Testosterone physiology in resistance exercise and training: the up-stream regulatory elements. Sports Med. 2010;40:1037–53. [DOI] [PubMed] [Google Scholar]
- 208.Courant F, Aksglaede L, Antignac J-P, Monteau F, Sorensen K, Andersson A-M, et al. Assessment of circulating sex steroid levels in prepubertal and pubertal boys and girls by a novel ultrasensitive gas chromatography-tandem mass spectrometry method. J Clin Endocrinol Metab. 2010;95(1):82–92. [DOI] [PubMed] [Google Scholar]
- 209.Herbst KL, Bhasin S. Testosterone action on skeletal muscle. Curr Opin Clin Nutr Metab Care. 2004;7(3):271–7. [DOI] [PubMed] [Google Scholar]
- 210.Van Every DW, D’Souza AC, Phillips SM. Hormones, hypertrophy, and hype: an evidence-guided primer on endogenous endocrine influences on exercise-induced muscle hypertrophy. Exerc Sport Sci Rev. 2024;52(4):117–25. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 211.Kanehisa H, Ikegawa S, Tsunoda N, Fukunaga T. Strength and cross-sectional areas of reciprocal muscle groups in the upper arm and thigh during adolescence. Int J Sports Med. 1995;16(01):54–60. [DOI] [PubMed] [Google Scholar]
- 212.Cormie P, McGuigan MR, Newton RU. Developing maximal neuromuscular power: part 1—biological basis of maximal power production. Sports Med. 2011;41:17–38. [DOI] [PubMed] [Google Scholar]
- 213.Behringer M, Vom Heede A, Yue Z, Mester J. Effects of resistance training in children and adolescents: a meta-analysis. Pediatrics. 2010;126(5):e1199–210. [DOI] [PubMed] [Google Scholar]
- 214.McCambridge TM, Stricker PR. Strength training by children and adolescents. Pediatrics. 2008;121(4):835–40. [DOI] [PubMed] [Google Scholar]
- 215.Moran J, Sandercock GR, Ramírez-Campillo R, Wooller J-J, Logothetis S, Schoenmakers PP, et al. Maturation-related differences in adaptations to resistance training in young male swimmers. J Strength Cond Res. 2018;32(1):139–49. [DOI] [PubMed] [Google Scholar]
- 216.Tomkinson GR, Carver KD, Atkinson F, Daniell ND, Lewis LK, Fitzgerald JS, et al. European normative values for physical fitness in children and adolescents aged 9–17 years: results from 2,779,165 Eurofit performances representing 30 countries. Br J Sports Med. 2018;52(22):1445–14563. [DOI] [PubMed] [Google Scholar]
- 217.Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee IM, et al. American College of Sports Medicine position stand. Quantity and quality of exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently healthy adults: guidance for prescribing exercise. Med Sci Sports Exerc. 2011;43(7):1334–59. [DOI] [PubMed] [Google Scholar]
- 218.Wong P-l, Chamari K, Wisløff U. Effects of 12-week on-field combined strength and power training on physical performance among U-14 young soccer players. J Strength Cond Res. 2010;24(3):644–52. [DOI] [PubMed] [Google Scholar]
- 219.Ramirez-Campillo R, Alvarez C, Gentil P, Loturco I, Sanchez-Sanchez J, Izquierdo M, et al. Sequencing effects of plyometric training applied before or after regular soccer training on measures of physical fitness in young players. J Strength Cond Res. 2020;34(7):1959–66. [DOI] [PubMed] [Google Scholar]
- 220.Alves AR, Marta CC, Neiva HP, Izquierdo M, Marques MC. Concurrent training in prepubescent children: the effects of 8 weeks of strength and aerobic training on explosive strength and VO2max. J Strength Cond Res. 2016;30(7):2019–32. [DOI] [PubMed] [Google Scholar]
- 221.Llanos-Lagos C, Ramirez-Campillo R, Moran J, Sáez de Villarreal E. Effect of strength training programs in middle- and long-distance runners’ economy at different running speeds: a systematic review with meta-analysis. Sports Med (Auckland, NZ). 2024;54(4):895–932. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 222.Llanos-Lagos C, Ramirez-Campillo R, Moran J, Sáez de Villarreal E. The effect of strength training methods on middle-distance and long-distance runners’ athletic performance: a systematic review with meta-analysis. Sports Med (Auckland, NZ). 2024;54(7):1801–33. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 223.Jones AM, Carter H. The effect of endurance training on parameters of aerobic fitness. Sports Med. 2000;29:373–86. [DOI] [PubMed] [Google Scholar]
- 224.Bassett DR, Howley ET. Limiting factors for maximum oxygen uptake and determinants of endurance performance. Med Sci Sports Exerc. 2000;32(1):70–84. [DOI] [PubMed] [Google Scholar]
- 225.Markovic G, Mikulic P. Neuro-musculoskeletal and performance adaptations to lower-extremity plyometric training. Sports Med (Auckland, NZ). 2010;40(10):859–95. [DOI] [PubMed] [Google Scholar]
- 226.Kubo K, Ikebukuro T, Yata H, Tsunoda N, Kanehisa H. Effects of training on muscle and tendon in knee extensors and plantar flexors in vivo. J Appl Biomech. 2010;26(3):316–23. [DOI] [PubMed] [Google Scholar]
- 227.Kubo K, Ikebukuro T, Yata H, Tsunoda N, Kanehisa H. Time course of changes in muscle and tendon properties during strength training and detraining. J Strength Cond Res. 2010;24(2):322–31. [DOI] [PubMed] [Google Scholar]
- 228.Paavolainen L, Häkkinen K, Hämäläinen I, Nummela A, Rusko H. Explosive-strength training improves 5-km running time by improving running economy and muscle power. J Appl Physiol (Bethesda, Md: 1985). 1999;86(5):1527–33. [DOI] [PubMed] [Google Scholar]
- 229.Bouamra M, Zouhal H, Ratel S, Makhlouf I, Bezrati I, Chtara M, et al. Concurrent training promotes greater gains on body composition and components of physical fitness than single-mode training (endurance or resistance) in youth with obesity. Front Physiol. 2022;13: 869063. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 230.Gäbler M, Prieske O, Hortobágyi T, Granacher U. The effects of concurrent strength and endurance training on physical fitness and athletic performance in youth: a systematic review and meta-analysis. Front Physiol. 2018;9:1057. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 231.Marta C, Marinho D, Barbosa TM, Izquierdo M, Marques M. Effects of concurrent training on explosive strength and VO2max in prepubescent children. Int J Sports Med. 2013:888–896. [DOI] [PubMed]
- 232.Li Z, Qi Y, Chen X, Li J, Zhang J, Li P, et al. Synergistic effects of concurrent aerobic and strength training on fitness in children and adolescents: a multivariate and network meta-analysis. Scand J Med Sci Sports. 2024;34(11): e14764. [DOI] [PubMed] [Google Scholar]
- 233.Hamill BP. Relative safety of weightlifting and weight training. J Strength Cond Res. 1994;8(1):53–7. [Google Scholar]
- 234.Myer GD, Quatman CE, Khoury J, Wall EJ, Hewett TE. Youth versus adult “weightlifting” injuries presenting to United States emergency rooms: accidental versus nonaccidental injury mechanisms. J Strength Cond Res. 2009;23(7):2054–60. [DOI] [PMC free article] [PubMed] [Google Scholar]

