Actively Recruiting
Creatine Supplementation in Young Healthy Adults
Led by University of Regina · Updated on 2024-09-20
42
Participants Needed
1
Research Sites
23 weeks
Total Duration
On this page
Sponsors
U
University of Regina
Lead Sponsor
I
Iovate Health Sciences International Inc
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose is to compare the effects of bolus ingestion (5 grams) vs. intermittent ingestion (2 x 2.5 grams) of creatine supplementation vs. placebo for 21 days on measures of body composition (lean tissue mass-indicator of muscle mass, total body water) and muscle performance (i.e., power, strength, endurance).
CONDITIONS
Official Title
Creatine Supplementation in Young Healthy Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 39 years
- Have not performed resistance training for at least 4 weeks before the study start
You will not qualify if you...
- Pregnant or nursing
- Taken creatine monohydrate within 30 days before the study start
- Allergic to the placebo (corn-starch maltodextrin)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Regina
Regina, Saskatchewan, Canada, S4S 0A2
Actively Recruiting
Research Team
D
Darren Candow
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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