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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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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.

James I Maynard, MSc contact

1 905 688-5550 ext. 5826

jm15mc@brocku.ca

Canada1 site, 1 recruiting
  • Brock University

    Saint Catharines, Ontario, L2S3A1

    Bareket Falk, PhD, 1-905-688-5550 ext. 4979, bfalk@brocku.ca

    Recruiting

Other trials in Canada

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).

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 groups in NCT07267429
Study groupRoleWhat they receive
TrainingActive comparatorresistance training, 12 weeks, 2 times per week
Receives: Other: Resistance training
ControlNo interventioncontinue with habitual physical activity

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. muscle strength

    1 repetition maximal - knee extension

    Measured: From enrollment to the end of training at 12 weeks

  2. 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)
  1. 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

  2. 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

  3. 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.

  1. First posted5 Dec 2025
  2. Study start1 Dec 2025
  3. Primary completionFeb 2026 (estimated)
  4. Study completionFeb 2026 (estimated)

Resources

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)
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

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.

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