Skip to content

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
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06604793
Enrollment
42
Registered
2024-09-20
Start date
2024-08-20
Completion date
2025-01-31
Last updated
2024-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Improve Muscle Performance in Young Adults

Brief 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.

Interventions

DIETARY_SUPPLEMENTCreatine

Creatine monohydrate

DIETARY_SUPPLEMENTPlacebo

Maltodextrin

Sponsors

University of Regina
Lead SponsorOTHER
Iovate Health Sciences International Inc
CollaboratorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 39 Years
Healthy volunteers
Yes

Inclusion criteria

* if you are 18-39 years of age * if you have not been performing resistance training for at least 4 weeks prior to the start of the study.

Exclusion criteria

* if you are pregnant or nursing * have taken creatine monohydrate within 30 days prior to the start of the study * if you have pre-existing allergies to the placebo (corn-starch maltodextrin)

Design outcomes

Primary

MeasureTime frameDescription
Whole-body lean mass (kg)baseline, day 21Bioelectrical impedance analysis
Strengthbaseline, day 211-repetition maximum leg press and chest press (kg)
Endurancebaseline, day 21Repetitions to fatigue for leg press and chest press (total number)
Hydrationbaseline, day 21Total body water (kg) using bioelectrical impedance analysis
Powerbaseline, day 21Vertical Jump (cm)

Countries

Canada

Contacts

Primary ContactDarren Candow
Darren.Candow@uregina.ca306-585-4906

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026