The Mito-Frail Trial: Effects of MitoQ on Vasodilation, Mobility and Cognitive Performance in Frail Older Adults
Part of paid clinical trials in Farmington, Connecticut.
- Sponsor
- UConn Health
- Study ID
- NCT06027554
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Aging
- Frailty
- Mild Cognitive Impairment
Eligibility Criteria
- Sex
- ALL
- Age
- 65 Years - 80 Years
- Healthy Volunteers
- Accepted
Interventions
- Mitoquinone Mesylate — DRUGMitoQ given 20 mg per day for 12 weeks.
- Placebo capsule — DIETARY_SUPPLEMENTPlacebo capsule taken every day for 12 weeks.
Study Details
The goal of this clinical trial is to test the effects of MitoQ supplementation in older adults and frail older adults with physical dysfunction and/or cognitive dysfunction. The main question\[s\] it aims to answer are: * To compare vascular function, oxidative stress levels, and physical and cognitive function among older adults and frail older adults with physical and cognitive dysfunction * To determine whether MitoQ supplementation has the potential to improve vascular function in central and cerebral vessels * To determine whether MitoQ supplementation can enhance physical and cognitive capabilities.
Key Dates
- Start date
- Oct 7, 2024
- Status verified
- Jan 2025
- Primary completion
- Mar 1, 2027
- Completion
- Feb 1, 2028
Study Design
- Enrollment
- 60 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- TREATMENT
Arms
- Placebo Comparator: Placebo capsuleGelatin capsules
- Experimental: MitoQ capsuleCapsules containing mitoquinone mesylate (MitoQ, 5 mg/capsule) totaling 20 mg taken every day for 12 weeks.
Primary Outcome Measure
Change in Vascular Endothelial Function [ Time Frame: 4 visits : Baseline, 12 weeks (MitoQ or Placebo), 8 weeks washout, 12 weeks (MitoQ or Placebo) ]
Central Contacts
- Oh Sung Kwon, PhD860-486-1120
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UConn Health | Farmington | Connecticut | 06030 |
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