Health-Related Quality of Life and Metabolic Outcomes in PCOS

  • STATUS
    Recruiting
  • End date
    Dec 31, 2027
  • participants needed
    40
  • sponsor
    The Cleveland Clinic
Send
Updated on 7 May 2026
See if I qualify
Accepts healthy volunteers

Summary

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.

Description

The proposed feasibility study seeks to test a short-term intervention focused on comprehensive PCOS (Polycystic Ovarian Syndrome) education and lifestyle modification support. The intervention, which will utilize an evidence-based PCOS curriculum, will be implemented by a multidisciplinary team of health providers via synchronous virtual group format.

Details
Condition PCOS (Polycystic Ovary Syndrome)
Age 18years - 49years
Clinical Study IdentifierNCT07571915
SponsorThe Cleveland Clinic
Last Modified on7 May 2026

Eligibility

 Yes No Not Sure

Inclusion Criteria

Non-pregnant females ages 18-49 years
Preexisting diagnoses of PCOS and obesity (body-mass index (BMI) equal or greater to 30 kg/m2) at enrollment

Exclusion Criteria

Patients who are pregnant or planning to become pregnant during the study period
Patients currently or with recent participation (< 12 months at the time of enrollment) in a PCOS-focused group
Patients with documented monogenic obesity
Patients with a diagnosis of any type of diabetes (with the exclusion of prediabetes)
Patients on systemic glucocorticoid therapy > 7 days at the time of enrollment
Patients with any end-stage organ disease
Patients without access to internet
Patients requiring English language interpretation
Any condition which, based on the investigator's medical judgment, would preclude patient ability to complete the study
Clear my responses
Read more

How to participate?

Step 1 Connect with a study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Email

View email

Phone

Phone country flag

View phone
Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Browse trials for

Accepts healthy volunteers

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.