Recruiting

Resistance Exercise

Sponsor:

Brock University

Code:

NCT06256744

Conditions

Dietary Supplementation

Exercise

Eligibility Criteria

Sex: All

Age: 7 - 35

Healthy Volunteers: Accepted

Interventions

exercise

Study Details

Brief summary:

Resistance exercise training (RET) in children and adolescents has become a popular area of research, with a growing body of evidence supporting its use. Position and consensus statements about RET for children indicate that it is safe and effective at increasing muscular strength, improving sport performance, and mitigating injury risk. 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. Nevertheless, some studies have suggested RET-induced muscle hypertrophy in children and adolescents, indicating that with certain training protocols, children may achieve muscle growth.

Hypertrophy of muscle fibres occurs when the rate of muscle protein synthesis (MPS) is greater than the rate of protein breakdown, and is enhanced with the ingestion of dietary amino acids. Due to ethical concerns with obtaining muscle samples (i.e., from muscle biopsies) in pediatric populations, MPS rates have not been previously assessed following RET in children. Recent advancements in stable-isotope methodology (specifically, leucine) allow for the estimation of MPS in a non-invasive breath test.

The objective of the proposed research is to examine the effects of an acute bout of RET on leucine retention (a proxy for MPS) in children, adolescents, and adults using a non-invasive breath test.

Conditions

Dietary Supplementation

Exercise

Study ID

NCT06256744

Start date

Sep, 2024

Status verified date

Aug, 2024

Completion date

Sep, 2025

Anticipated

Primary completion date

Aug, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 7 - 35

Healthy Volunteers: Accepted

Inclusion Criteria:

  • healthy
  • free of injury that would prevent resistance exercise

Exclusion Criteria:

  • consumed any medications in the past year which may affect muscle function
  • had an injury in the past 6 months that would limit the movements required for the protocols
  • been told that has diabetes
  • been told that had a heart problem
  • been told that have a breathing problem (e.g., asthma)
  • been told that sometimes experience seizures
  • had joint instability or ongoing join chronic pain
  • been told that had kidney problems
  • had stomach problems such as ulcers
  • experience prolonged bleeding after a cut

Study Design

Enrollment

60 participants

Anticipated

Intervention Model

Single group

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

experimental: Protein supplementation

Protein supplementation

Interventions

exercise

Resistance exercise

Primary outcome measure

  • Leucine retention [ Time Frame: During the experimental session, expired air is collected pre-ingestion and every 30minutes. i.e., at -60, 0, 30, 60, 90, 120, 150, 180, 210, 240, 270, 300 minutes. ]

Central Contacts and Locations

Central contacts

Locations

Brock University

Recruiting

St. Catharines, Ontario, Canada, L2S3A1

More Information

Sponsor

Brock University

Last update posted

Aug 16, 2024

Last verified

Aug, 2024

Keywords

  • Children
  • Muscle
  • Protein
  • Resistance training

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Brock University on 2024-08-16.