Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06604793

Creatine Supplementation in Young Healthy Adults

Effects of Equal-volume Creatine Supplementation With Different Dosing Strategies on Body Composition and Muscle Performance in Young Healthy Adults

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
42 (estimated)
Sponsor
University of Regina · Academic / Other
Sex
All
Age
18 Years – 39 Years
Healthy volunteers
Accepted

Summary

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).

Detailed description

Creatine is a naturally occurring compound produced in the liver and brain. Creatine can also be found in food products such as red meat and seafood or through commercially available manufactured creatine products (i.e. creatine supplementation). Evidence-based research shows that creatine supplementation improves measures of body composition and muscle performance. However, the optimal creatine supplementation protocol to achieve these benefits is unknown.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCreatineCreatine monohydrate
DIETARY_SUPPLEMENTPlaceboMaltodextrin

Timeline

Start date
2024-08-20
Primary completion
2025-01-31
Completion
2025-01-31
First posted
2024-09-20
Last updated
2024-09-20

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06604793. Inclusion in this directory is not an endorsement.