Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Illinois at Chicago
Age
18–45
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
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 (ovarian volume \>10 cc and /or antral follicle count 20 in at least one ovary); and (iii) chronic oligo-amenorrhea (intermenstrual intervals \>35 days or 7 periods/year)
BMI between 25-50 kg/m2
Age between 18-45 years
You may not be if
Postmenopausal (absence of menses for \>2 y)
Diagnosed type 1 diabetes or type 2 diabetes
Previously diagnosed with a mood depressive disorder (by a doctor or psychologist)
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
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 currently following a TRE protocol
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
Clareo Health | Time Restricted Eating for the Treatment of PCOS
