Actively Recruiting
The Effects of Cold-water Immersion on Exercise Performance Recovery and Postprandial Plasma Aminoacidemia
Led by McGill University · Updated on 2026-04-09
12
Participants Needed
1
Research Sites
88 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In order to optimize sports performance, high-level athletes are required to manage conflicting training objectives, which often result in periods of high-volume training. These athletes need to perform heavy resistance training sessions to promote physiological adaptations, which consequently induce fatigue. Yet, they need to minimize fatigue to perform subsequent high-quality training sessions often within the same day. To support these training endeavours, a high-quality dietary regimen and adequate protein consumption is deemed to be an essential component of an athlete's recovery plan, as it has been shown to support muscle recovery and reduce muscle inflammation following exercise. Indeed, current sports nutrition recommendations advocate for the consumption of dietary protein and carbohydrate after exercise to promote tissue repair and replenish muscle energy stores (glycogen). Additionally, previous research has shown how water immersion therapies post-exercise may alleviate fatigue and restore performance. However, little is known about how different temperatures, as well as timing of cold-water immersion can support performance recovery in a population of athletes adhering to contemporary post-exercise nutrition recommendations. The objective of this project is to investigate the effects of timing of cold-water immersion relative to exercise on performance recovery within the same day, as well as to investigate whether cold water immersion augments blood amino acid concentrations after exercise and protein intake.
CONDITIONS
Official Title
The Effects of Cold-water Immersion on Exercise Performance Recovery and Postprandial Plasma Aminoacidemia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy adults aged 18 to 40 years (inclusive)
- Body mass index (BMI) between >18.5 and <30 kg/m2 (inclusive)
- In good general health with no uncontrolled diseases or conditions
- History of regular resistance training at least twice per week for the past six months
- Currently competing at varsity, provincial, national, or international levels in their sport
- Free from musculoskeletal injuries or conditions affecting exercise or cold-water immersion
- Stable use of medications, supplements, diet, lifestyle, and body weight (weight change <3 kg) over the past three months
- Agree to maintain usual training habits between study sessions
You will not qualify if you...
- Pregnant, lactating, or planning pregnancy during the study
- Females with irregular menstrual cycles outside 24-38 days
- Following a diet that restricts dairy consumption (e.g., vegan)
- Known allergy or intolerance to study products or lactose
- Weight change greater than 3 kg in the three months before study start
- Currently on or planning a weight loss regimen during the study
- Recent acute gastrointestinal illness within two weeks prior to screening
- History of gastrointestinal diseases, surgeries (excluding appendectomy or herniorrhaphy), or disorders
- Abnormalities or obstructions affecting swallowing or digestion
- Recent upper gastrointestinal procedures within three months prior to screening
- Diagnosed hypercholesterolemia or hypertriglyceridemia
- History of heart or cardiovascular disease, uncontrolled hypertension, kidney or liver disease
- Diabetes (Type I, Type II, or pre-diabetic) or elevated blood glucose or hemoglobin A1c
- History of liver, gallbladder disease, or stomach ulcers
- Unstable thyroid disease, major psychiatric disorders, immune disorders, or immunocompromised status
- Cancer diagnosed within five years except certain localized cancers
- Major surgery within three months prior or planned during the study
- History of alcohol or substance abuse within 12 months
- Tobacco use within the last six months
- Recent blood or plasma donation within defined time frames
- Other active or unstable medical conditions or treatments posing risk or affecting study participation
AI-Screening
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Trial Site Locations
Total: 1 location
1
McGill University
Montreal, Quebec, Canada, H2W 1S4
Actively Recruiting
Research Team
T
Tyler Churchward-Venne, PhD
CONTACT
T
Thalia Krauth-Ibarz, BSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
3
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