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The Effect of Exercise and Presleep Nutrition on Muscle Connective Tissue Remodelling

The Effect of Exercise and Presleep Nutrition on Muscle Connective Tissue Remodelling

Recruiting
18-35 years
All
Phase N/A

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Overview

The primary objective of this study will be to determine the influence of a presleep vitamin C-enriched, collagen-modelled supplement (CVC) on the metabolic fate of dietary glycine using a [2H5]glycine tracer within the intramuscular connective tissue at rest and after a bout of resistance exercise. Other outcomes will be related to regulation collagen remodelling in skeletal muscle.

Eligibility

Inclusion Criteria:

  • Healthy, recreationally active, male and female participants.
  • Healthy will be defined as someone who does not have a health condition that would compromise their ability to safely participate in the strenuous physical activity involved in our study as screened for by the Get Active Questionnaire.
  • Willing to abstain from resistance exercise for 2 weeks prior to the first metabolic trial and for the duration of the study.
  • Participants must be able to abstain from lower-body resistance and/or plyometric exercise for at least 2 weeks prior to the first metabolic trial.
  • Participants will be aged 18-35 years old.
  • Participants must be normal to overweight (e.g., BMI 18.5-30).
  • Participants are willing to abide by the compliance rules of this study (e.g., abstain from physical activity and alcohol 48h prior to each trial).
  • Self-reported regular menstrual cycle (25-35d) within the last 3 months (female participants).

Exclusion Criteria:

  • Inability to adhere to any of the compliance rules judged by principal investigator or medical doctor.
  • Self-reported regular tobacco use.
  • Self-reported illicit drug use (e.g. growth hormone, testosterone, etc.).
  • Regular use of anti-inflammatory drugs (e.g., ibuprofen).
  • Self-reported regularly sleeping less than an average of 7 hours over 3 days (minimum recommended daily amount).
  • Individuals who have participated in studies within the past year involving any of the stable isotopes in the study.
  • Use of birth control and discontinued use in the last 3-months (female only).

Study details
    Interventional

NCT06054620

University of Toronto

26 January 2024

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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