Healthy ParticipantsB-STRONGNCT07267429
Resistance Training-induced Adaptations in Children
A study testing Resistance training in people with Healthy Participants, run by Brock University at 1 site in Canada.
Trial summary
Resistance exercise training (RET) in children and adolescents has become a popular activity, with a growing body of evidence supporting its use. Numerous studies indicate that it is safe and effective at increasing muscular strength, improving sport performance, and mitigating injury risk. Read more about this study
- Who is it for?
- Ages 7 to 12 yearsHealthy volunteers can take part
- Conditions the study is for
- Healthy Participants
- What is being tested?
- Resistance training
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 siteCanada
- Study dates
- 1 Dec 2025to Feb 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 7 to 12 years
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- healthy
- able to exercise
Who cannot join
- have consumed any medications in the past year which may affect muscle function,
- have any prior injuries or medical diagnoses associated with altered muscular function,
- have had an injury in the past 6 months that would limit the movements required for the training and assessment protocols,
- have performed resistance training in the past 6 months or currently participate in competitive sports (i.e., outside of school) more than 2x/week.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Canada1 site, 1 recruiting
- Recruiting
Brock University
Saint Catharines, Ontario, L2S3A1
Bareket Falk, PhD, 1-905-688-5550 ext. 4979, bfalk@brocku.ca
About this study
Resistance exercise training (RET) in children and adolescents has become a popular activity, with a growing body of evidence supporting its use. Numerous studies indicate that it is safe and effective at increasing muscular strength, improving sport performance, and mitigating injury risk. Despite this evidence, there are still many unknowns with RET in children, including its mechanisms of action in enhancing muscle strength.
Neural and muscular mechanisms can improve muscle strength following RET. Neural factors include improved recruitment and firing of an individual's muscle cells, and muscular factors primarily include an increase in the size of the muscle (hypertrophy). In children, little is known about how these mechanisms relate to muscle strength.
Therefore, the purpose of this study is to non-invasively assess the mechanisms of RET-induced strength increases in children performing 12 weeks of RET, compared with a non-training control group. Broadly, muscular adaptations will be assessed using ultrasound measures, while neural mechanisms will be assessed using surface electromyography decomposition.
Read the detailed description
Resistance exercise training (RET) in children and adolescents has become a popular activity, with a growing body of evidence supporting its use. Position and consensus statements on RET for children indicate that it is safe and effective at increasing muscular strength, improving sport performance, and mitigating injury risk. Despite this evidence, there are still many unknowns with RET in children, including its mechanisms of action in enhancing muscle strength.
Neural and muscular mechanisms can improve muscle strength following RET. Neural factors include improved recruitment and firing of an individual's motor units, and muscular factors primarily include an increase in the size of the muscle (hypertrophy). In children, little is known about how these mechanisms relate to muscle strength. There is very little evidence of morphological changes following RET in children. Therefore, conventional wisdom is that children rely only on neural factors to improve strength following RET, possibly due to their lower levels of circulating androgens. Nevertheless, some studies have suggested RET-induced muscle hypertrophy in children and adolescents, indicating that with certain training protocols, and with more-sensitive research methods, children may achieve RET-induced muscle growth.
The neural mechanisms that presumably improve the muscle strength of children following RET are also largely unknown. Previously, global surface electromyography (sEMG) has been utilized to observe changes in overall muscle activation. However, this measure is unspecific and can be influenced by neural and morphological adaptations. Recent advancements in sEMG decomposition - which separates the sEMG signal into the discrete motor units it is composed of - allow for more specific neural adaptations to be assessed non-invasively. To date, this technological advancement has only been utilized in two studies to assess neuromuscular adaptations to RET in youths, with inconsistent results.
Therefore, the purpose of this study is to non-invasively assess the mechanisms of RET-induced strength increases in children performing 12 weeks of RET, compared with a non-training control group. Broadly, morphological adaptations will be assessed using ultrasound measures, while neural mechanisms will be assessed using sEMG decomposition. In addition to these primary outcomes, the effects of RET in children on cardiovascular regulation.
Procedures Participants will be required to make three pre-intervention, two mid-intervention, and two post-intervention visits to the Applied Physiology/Sympathetic Neurocirculatory Regulation Laboratories at Brock University for the completion of all testing procedures. The mid-intervention visits will be during the fourth and eighth weeks (1 session each), and the post intervention visits will be within one week following the completion of the intervention (2 sessions).
The first pre-intervention visit will serve as the familiarization session. Questionnaires will be completed to screen for medical concerns, assess pubertal stage, athletic training practices, menarcheal status (females only), self perception, habitual eating habits, and habitual physical activity. These questionnaires will be repeated following the intervention period. Following the completion of questionnaires, participants will be familiarized with the muscular strength/contraction tests that will be performed in the remaining testing sessions.
Four of the remaining testing sessions (1 pre-intervention, 2 mid-intervention, and 1 post-intervention) will include body measures and muscular strength/contraction tests that will serve as the primary experimental outcomes. Finally, one of the pre- and post-intervention sessions will include the assessment of blood flow and pressure regulation, to see how these are affected by RET.
The RET protocol will include twice weekly RET sessions for 12 weeks, using exercise machines. Each session will consist of ~5-10 minutes of warm-up, ~40-50 minutes of resistance training exercises, and ~5-10 minutes of cool down. The program will primarily focus on exercise machines for the lower body; however, some free weight and upper body exercises will be incorporated to maintain the interest of the participants and to ensure a whole-body workout. Exercises will be completed at varying intensities and volumes, but generally between 60-85% 1RM for ~6-15 repetitions. When the desired number of repetitions can be performed by a participant safely and with appropriate technique, the intensity (e.g., weight) of the exercise will be progressed. Some examples of exercise that will be of focus in the training protocol will include the leg press, leg extension, and leg curl. Prior to the administering the intervention, participants will be properly shown how to safely conduct each exercise in a controlled and safe manner.
Participants in the proposed study will be male and female children (~7-12 years).
- Conditions
- Healthy Participants
- Being tested
- Resistance training
- Keywords
- Strength training, Resistance training
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Resistance trainingOther
progressive resistance training, 12 weeks, 2 times per week
| Study group | Role | What they receive |
|---|---|---|
| Training | Active comparator | resistance training, 12 weeks, 2 times per week Receives: Other: Resistance training |
| Control | No intervention | continue with habitual physical activity |
What is being measured
The primary outcome is the main question the study is designed to answer.
muscle strength
1 repetition maximal - knee extension
Measured: From enrollment to the end of training at 12 weeks
Peak torque
Peaktorque will be measured during isokinetic and isometric maximal contractions of the knee extensors
Measured: From enrollment to end of training at 12 weeks
Secondary outcomes (3)
Motor unit activation
Surface electromyography signal during a ramped contraction will be used to assess changes in motor unit firing rates
Measured: from enrollment to end of training at 12 weeks
muscle cross sectional area
B-mode ultrasound will be used to capture panoramic images of multiple muscles of the thigh. These images will be used to assess changes in muscle cross sectional area.
Measured: from enrollment to end of training at 12 weeks
Blood pressure regulation
Blood pressure will be assessed before and after maximal voluntary apnea, as well as before and after isometric handgrip exercise.
Measured: from enrollment to end of training at 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Dec 2025
- Study start1 Dec 2025
- Primary completionFeb 2026 (estimated)
- Study completionFeb 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Healthy ParticipantsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Brock University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Bareket Falk, Brock University
- Investigators
- Bareket Falk, PhD, Principal investigator, Brock University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07267429
- Sponsor's protocol ID
- B-STRONG
- Acronym
- B-STRONG
- Status last verified
- Dec 2025
- First submitted
- 25 Nov 2025
- Last updated
- 15 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Participation is confidential
Study at a glance
From the registry record, last updated by the sponsor on 15 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Resistance Training-induced Adaptations in Children
- ClinicalTrials.gov ID
- NCT07267429
- Acronym / sponsor ID
- B-STRONG / B-STRONG
- Conditions
- Healthy Participants
- Keywords
- Strength training, Resistance training
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Brock UniversityUniversity, hospital or other
- Study start
- 1 Dec 2025 (actual)
- Primary completion
- Feb 2026 (estimated)
- Study completion
- Feb 2026 (estimated)
- First posted
- 5 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Resistance exercise training (RET) in children and adolescents has become a popular activity, with a growing body of evidence supporting its use. Numerous studies indicate that it is safe and effective at increasing muscular strength, improving sport performance, and mitigating injury risk. Despite this evidence, there are still many unknowns with RET in children, including its mechanisms of action in enhancing muscle strength.
Neural and muscular mechanisms can improve muscle strength following RET. Neural factors include improved recruitment and firing of an individual's muscle cells, and muscular factors primarily include an increase in the size of the muscle (hypertrophy). In children, little is known about how these mechanisms relate to muscle strength.
Therefore, the purpose of this study is to non-invasively assess the mechanisms of RET-induced strength increases in children performing 12 weeks of RET, compared with a non-training control group. Broadly, muscular adaptations will be assessed using ultrasound measures, while neural mechanisms will be assessed using surface electromyography decomposition.
Detailed description
Resistance exercise training (RET) in children and adolescents has become a popular activity, with a growing body of evidence supporting its use. Position and consensus statements on RET for children indicate that it is safe and effective at increasing muscular strength, improving sport performance, and mitigating injury risk. Despite this evidence, there are still many unknowns with RET in children, including its mechanisms of action in enhancing muscle strength.
Neural and muscular mechanisms can improve muscle strength following RET. Neural factors include improved recruitment and firing of an individual's motor units, and muscular factors primarily include an increase in the size of the muscle (hypertrophy). In children, little is known about how these mechanisms relate to muscle strength. There is very little evidence of morphological changes following RET in children. Therefore, conventional wisdom is that children rely only on neural factors to improve strength following RET, possibly due to their lower levels of circulating androgens. Nevertheless, some studies have suggested RET-induced muscle hypertrophy in children and adolescents, indicating that with certain training protocols, and with more-sensitive research methods, children may achieve RET-induced muscle growth.
The neural mechanisms that presumably improve the muscle strength of children following RET are also largely unknown. Previously, global surface electromyography (sEMG) has been utilized to observe changes in overall muscle activation. However, this measure is unspecific and can be influenced by neural and morphological adaptations. Recent advancements in sEMG decomposition - which separates the sEMG signal into the discrete motor units it is composed of - allow for more specific neural adaptations to be assessed non-invasively. To date, this technological advancement has only been utilized in two studies to assess neuromuscular adaptations to RET in youths, with inconsistent results.
Therefore, the purpose of this study is to non-invasively assess the mechanisms of RET-induced strength increases in children performing 12 weeks of RET, compared with a non-training control group. Broadly, morphological adaptations will be assessed using ultrasound measures, while neural mechanisms will be assessed using sEMG decomposition. In addition to these primary outcomes, the effects of RET in children on cardiovascular regulation.
Procedures Participants will be required to make three pre-intervention, two mid-intervention, and two post-intervention visits to the Applied Physiology/Sympathetic Neurocirculatory Regulation Laboratories at Brock University for the completion of all testing procedures. The mid-intervention visits will be during the fourth and eighth weeks (1 session each), and the post intervention visits will be within one week following the completion of the intervention (2 sessions).
The first pre-intervention visit will serve as the familiarization session. Questionnaires will be completed to screen for medical concerns, assess pubertal stage, athletic training practices, menarcheal status (females only), self perception, habitual eating habits, and habitual physical activity. These questionnaires will be repeated following the intervention period. Following the completion of questionnaires, participants will be familiarized with the muscular strength/contraction tests that will be performed in the remaining testing sessions.
Four of the remaining testing sessions (1 pre-intervention, 2 mid-intervention, and 1 post-intervention) will include body measures and muscular strength/contraction tests that will serve as the primary experimental outcomes. Finally, one of the pre- and post-intervention sessions will include the assessment of blood flow and pressure regulation, to see how these are affected by RET.
The RET protocol will include twice weekly RET sessions for 12 weeks, using exercise machines. Each session will consist of ~5-10 minutes of warm-up, ~40-50 minutes of resistance training exercises, and ~5-10 minutes of cool down. The program will primarily focus on exercise machines for the lower body; however, some free weight and upper body exercises will be incorporated to maintain the interest of the participants and to ensure a whole-body workout. Exercises will be completed at varying intensities and volumes, but generally between 60-85% 1RM for ~6-15 repetitions. When the desired number of repetitions can be performed by a participant safely and with appropriate technique, the intensity (e.g., weight) of the exercise will be progressed. Some examples of exercise that will be of focus in the training protocol will include the leg press, leg extension, and leg curl. Prior to the administering the intervention, participants will be properly shown how to safely conduct each exercise in a controlled and safe manner.
Participants in the proposed study will be male and female children (~7-12 years).
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Training | Active comparator | Other: Resistance trainingresistance training, 12 weeks, 2 times per week |
| Control | No intervention | –continue with habitual physical activity |
Who may qualify
- Ages
- 7 to 12 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (2 listed)
- healthy
- able to exercise
Key exclusion criteria (4 listed)
- have consumed any medications in the past year which may affect muscle function,
- have any prior injuries or medical diagnoses associated with altered muscular function,
- have had an injury in the past 6 months that would limit the movements required for the training and assessment protocols,
- have performed resistance training in the past 6 months or currently participate in competitive sports (i.e., outside of school) more than 2x/week.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Resistance trainingprogressive resistance training, 12 weeks, 2 times per week | Other | Training |
Primary outcome
muscle strength
Time frame: From enrollment to the end of training at 12 weeks
1 repetition maximal - knee extension
Peak torque
Time frame: From enrollment to end of training at 12 weeks
Peaktorque will be measured during isokinetic and isometric maximal contractions of the knee extensors
3 secondary outcomes
Motor unit activation
Time frame: from enrollment to end of training at 12 weeks
muscle cross sectional area
Time frame: from enrollment to end of training at 12 weeks
Blood pressure regulation
Time frame: from enrollment to end of training at 12 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Dec 2025.
- Individual participant dataSharing planned: No. Participation is confidential
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Bareket Falk, PhD principal investigator
Brock University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Resistance training in people with Healthy Participants, run by Brock University at 1 site in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 15 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Andrew McKiel, MSc (1 905 688-5550 ext. 5826, am20ff@brocku.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
muscle strength (time frame: From enrollment to the end of training at 12 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Dec 2025.