Creatine for Recovery and Thinking in Mothers
Part of paid clinical trials in Chapel Hill, North Carolina.
- Sponsor
- University of North Carolina, Chapel Hill
- Study ID
- NCT07795853
- Status
- Not Yet Recruiting
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Conditions
- Post-partum
- Women
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 45 Years
- Healthy Volunteers
- Not accepted
Interventions
- Creatine Monohdyrate — DIETARY_SUPPLEMENTCreatine monohydrate taken daily mixed with 6-8 oz of water.
Study Details
The purpose of this randomized, double-blind, parallel-group trial is to compare the effects of two doses of creatine monohydrate (5 g/day versus 10 g/day) administered for four weeks in postpartum women. The study will evaluate exercise performance, post-exercise recovery, cognitive function, and brain creatine concentrations in a sub-sample.
Key Dates
- First listed
- Aug 31, 2026
- Start date
- Sep 8, 2026
- Status verified
- Aug 2026
- Primary completion
- May 10, 2027
- Completion
- May 10, 2027
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: Low-Dose Creatine MonohydrateParticipants consume 5 grams per day of creatine monohydrate for 28 consecutive days.
- Experimental: High-dose Creatine MonohydrateParticipants consume 10 grams per day of creatine monohydrate for 28 consecutive days.
Primary Outcome Measure
Repeated Sprint Ability Peak Power [ Time Frame: Change from baseline to 4 weeks post-supplementation. ]
Central Contacts
- Abbie Smith-Ryan, PhD919-962-2574
- Research Coordinator919-962-1663
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Applied Physiology Laboratory | Chapel Hill | North Carolina | 27599 | Abbie Smith-Ryan, PhD (PRINCIPAL_INVESTIGATOR) |
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