Weight Loss Intervention in Women With PCOS

Completed · Not applicable

Conditions studied: Polycystic Ovary Syndrome, Overweight and Obesity

In brief

The proposed single arm 6 mo. trial will assess the impact of weight loss and fat loss due to a multicomponent remotely-delivered lifestyle intervention on ovulation rates and time-to-ovulation in overweight and obese women with anovulatory infertility caused by PCOS.

Key facts

Study ID

NCT03677362

Run by

University of Kansas Medical Center

People needed

12

Starts

2018-09-10

Expected to finish

2020-02-22

Last updated by the study team

2020-09-01

Who can join

Age: 21 and older, up to 42. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Anovulatory infertility caused by Polycystic ovarian syndrome
• Age 21 to 42.
• Body mass index (BMI) > 25 to 45 kg/m2.
• Weight stable (± 4.6 kg) in previous 3 months
• Willing to delay fertility treatment for 6 mos

You may not qualify if…

• Unable to participate in moderate-vigorous physical activity (i.e., brisk walking)
• Currently participating in greater than 3, 30-minute bouts of planned PA/week
• Participation in a weight loss or PA program in the previous 6 mos.
• Currently on a weight loss medication (wash out period 2 mos.)
• Any other infertility diagnosis besides ovulatory dysfunction
• Binge eating disorder as assessed by the Binge Eating Scale.

Where it is running

• University of Kansas Medical Center — Kansas City, Kansas, United States

Full record on ClinicalTrials.gov

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