Time Restricted Eating for the Treatment of PCOS
Polycystic Ovary Syndrome, Obesity
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome
Eligibility Criteria
Inclusion criteria: Diagnosed with PCOS based on the Rotterdam criteria in which two of three of the following criteria are present: (i) androgen excess skin manifestations (hirsutism, acne, and seborrhea) and/or hyperandrogenemia (total testosterone >55 pg/ml, free testosterone >9.4 pg/ml, androstenedione >2.1 ng/ml or DHEA-S >340 ug/dl); (ii) polycystic ovarian morphology on ultrasound; and (iii) chronic oligo-amenorrhea (intermenstrual intervals >35 days or 7 periods/year) BMI between 25-50 kg/m2 Age between 18-40 years Exclusion criteria: Postmenopausal (absence of menses for >2 y) Diagnosed type 1 diabetes or type 2 diabetes Have a history of eating disorders (anorexia, bulimia, or binge eating disorder) Are not weight stable for 3 months prior to the beginning of the study (weight gain or loss > 4 kg) Are taking drugs that affect study outcomes, such as oral contraceptives, weight loss, insulin-sensitizing agents, androgen antagonists, anti-seizure, or antipsychotic medication (within 2 months of starting study) Are athletes or those engaging in >1 hour of high-intensity training on more than 5 days/week Are active smokers (within 3 months of starting the study) Do not have a Wi-Fi connection at home (needed for zoom calls) Pregnant or trying to become pregnant
Sites / Locations
- University of Illinois Chicago
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
6-hour Time restricted eating (TRE)
Calorie restriction (CR)
Control
Ad libitum food intake from 1-7 pm every day Fasting from 7-1 pm every day (18-h fast)
25% energy restriction every day
Usual diet