- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06431334
Protein Requirements Amongst Male Masters-Level Athletes Following a Cycling Exercise Bout as Determined by the Indicator Amino Acid Oxidation Technique
Masters level cyclists are a population above the age of 35 years who frequently participate in prolonged as well as heavy-volume training. Like most endurance-trained athletes, a greater recommended dietary allowance (RDA) for protein of 1.2-1.4 g/kg/bw is suggested.
Dietary protein intake is vital for maximizing the benefits of training and ensuring optimal recovery. Dietary recommendations traditionally have been determined through nitrogen balance techniques, however, recent research indicates how this method is potentially underestimating protein requirements. Therefore, there is a need to reassess current dietary recommendations in order to meet the demands of physical activity for highly active populations.
Recent efforts to understand protein requirements during rest and following exercise have been completed using the indicator amino acid technique (IAAO). This non-invasive method is reported to provide a robust measure of protein requirements. However, there is limited work in older (≥60 years) active populations.
The purpose of this study is to measure the protein requirements in master cyclists, following an endurance training session, using the non-invasive IAAO technique.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tyler A. Churchward-Venne, Ph.D.
- Phone Number: 00839 (514) 398-4184
- Email: tyler.churchward-venne@mcgill.ca
Study Contact Backup
- Name: Damian Papadopoulos, B.Sc
- Phone Number: (514) 561-7860
- Email: damian.papadopoulos@mail.mcgill.ca
Study Locations
-
-
Quebec
-
Montreal, Quebec, Canada, H3A 0G4
- Recruiting
- McGill University
-
Contact:
- Tyler Churchward-Venne, PhD
- Phone Number: (514) 399-9684
- Email: tyler.churchward-venne@mcgill.ca
-
Principal Investigator:
- Tyler Churchward-Venne, PhD
-
Sub-Investigator:
- Damian Papadopoulos, BSc
-
Contact:
- Damian Papadopoulos, B.Sc.
- Phone Number: 5145617860
- Email: damian.papadopoulos@mail.mcgill.ca
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 18.5< BMI <35 kg/m^2
- Overtly healthy masters level cyclists ≥65 years
- Masters level cyclist training (>4 days per week; ~100 km per week)
- Body mass stable over previous 6-months
- Availability for multiple metabolic trials (~7 trials)
- Ability to travel to and from laboratory facility
Exclusion Criteria:
- Recent history of weight loss or weight gain (>5% body weight)
- Uncontrolled hypertension
- ≥2 chronic diseases (e.g. diabetes, osteoporosis, dyslipidemia)
- Acute illness that could affect protein metabolism (HIV, renal dysfunction, influenza)
- Currently using anti-inflammatory medications
- Inability to adhere to study protocol (i.e., alcohol, caffeine, dietary restrictions)
- Regular tobacco user
- Illicit drug use
- Habitually ingesting ≥3 g/kg/bw
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Masters Level Cyclists
Participants are to be randomly assigned varying levels of amino acid intakes ranging between 0.2 to 2.8 g/kg/d
|
Amino acid intakes will vary between 0.2 to 2.8 g/kg/d
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
13CO2 Excretion
Time Frame: 7-weeks
|
Measured by continuous-flow isotope ratio mass spectrometry
|
7-weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
L[13C]phenylalanine Oxidation
Time Frame: 7-weeks
|
Measured by gas chromatography-mass spectrometry
|
7-weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- A06-M25-23A
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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