Health-Related Quality of Life and Metabolic Outcomes in PCOS

Part of paid clinical trials in Cleveland, Ohio.

Sponsor
The Cleveland Clinic
Study ID
NCT07571915
Status
Recruiting
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Conditions

  • PCOS (Polycystic Ovary Syndrome)

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 49 Years
Healthy Volunteers
Accepted

Interventions

  • Intervention Group — OTHER
    Short term comprehensive PCOS education coupled with lifestyle modification support

Study Details

The primary outcome of interest is change in PCOS health-related quality of life, while the secondary outcome of interest is change in adiposity, cardiometabolic, and inflammation biomarkers.

Key Dates

Start date
May 23, 2026
Status verified
Apr 2026
Primary completion
May 1, 2027
Completion
Dec 31, 2027

Study Design

Enrollment
40 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • No Intervention: Standard of Care
    Participants will complete seca mBCA (medical Body Composition Analyzer), lab workup, and questionaries
  • Experimental: Intervention Group
    Participants will complete a seca mBCA (medical Body Composition Analyzer), lab workup, and questionaries Short term comprehensive PCOS education coupled with lifestyle modification support

Primary Outcome Measure

Difference in Modified PCOS Health-related Quality of life questionnaire (mPCOSQ) scoring between participants. [ Time Frame: 4 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Cleveland ClinicClevelandOhio44195
Amber Sike
[email protected]
216-444-7551
Andrea Parianos
[email protected]
216-445-8354

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