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Time Restricted Eating for the Treatment of PCOS

Primary Purpose

Polycystic Ovary Syndrome, Obesity

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
6-h Time restricted eating (TRE)
Calorie restriction (CR)
Control
Sponsored by
University of Illinois at Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polycystic Ovary Syndrome

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

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

Arm Type

Experimental

Experimental

Experimental

Arm Label

6-hour Time restricted eating (TRE)

Calorie restriction (CR)

Control

Arm Description

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

Outcomes

Primary Outcome Measures

Change in body weight
Measured by an electronic scale

Secondary Outcome Measures

Change in fat mass, lean mass, visceral fat mass
Measured by DXA
Change in bone mineral density
Measured by DXA
Change in waist circumference
Measured by a measuring tape
Change in Insulin sensitivity
Measured by oral glucose tolerance test (OGTT)
Change in Fasting glucose
Measured by a commercial lab (Medstar, IL)
Change in Fasting insulin
Measured by a commercial lab (Medstar, IL)
Change in HbA1c
Measured by a commercial lab (Medstar, IL)
Change in Blood pressure
Measured by a blood pressure cuff
Change in heart rate
Measured by a blood pressure cuff
Change in Plasma lipids (LDL cholesterol, HDL cholesterol, triglycerides)
Measured by a commercial lab (Medstar, IL)
Change in inflammatory markers (TNF-apha, IL-6, IL-10, IL-B, hs-CRP)
Measured by ELISA
Change in oxidative stress (8-isoprostane)
Measured by ELISA
Change in reproductive hormones (testosterone, DHEA, SHBG, androstenedione)
Measured by ELISA
Change in energy and nutrient intake
Measured by 7-day food record
Change in physical activity (steps/d)
Measured by pedometer
Change in mood
Measured by 36-Item Short Form Survey (SF-36), total score 0-100. Higher scores mean worse outcome.
Change in appetite
Measured by Visual analog scale (VAS). Scored from 0-100. Higher score means higher appetite.

Full Information

First Posted
November 17, 2022
Last Updated
May 8, 2023
Sponsor
University of Illinois at Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT05629858
Brief Title
Time Restricted Eating for the Treatment of PCOS
Official Title
Time Restricted Eating for the Treatment of Polycystic Ovarian Syndrome (PCOS)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
January 15, 2023 (Actual)
Primary Completion Date
January 1, 2028 (Anticipated)
Study Completion Date
January 1, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Illinois at Chicago

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Polycystic ovary syndrome (PCOS) is the most common cause of anovulatory infertility among young women. This syndrome is a reproductive and endocrinological disorder that affects up to 18% of reproductive-aged women. To date, the only strategy shown to reverse PCOS is sustained weight loss of 5-10%. At present, daily calorie restriction (CR) is the main diet prescribed to patients with PCOS for weight loss. However, some women find it difficult to adhere to CR because calorie intake must be vigilantly monitored every day. Considering these problems with CR, another approach that limits timing of food intake, instead of number of calories consumed, has been developed. This diet is called "time restricted eating" (TRE) and involves confining the period of food intake to 6-8 h per day. TRE allows individuals to self-select foods and eat ad libitum during a large part of the day, which greatly increases compliance to these protocols. Recent findings show that TRE significantly reduces body weight, insulin resistance, and inflammation in adults with obesity. However, no randomized controlled trials have studied the role of TRE in treating PCOS. Accordingly, this study will compare the effects of TRE vs CR in females with PCOS over 6 months on body weight, androgen markers, inflammatory markers and insulin sensitivity. Methods: A 6-month randomized, controlled, parallel-arm trial will be implemented. Females with obesity and PCOS will be randomized to 1 of 3 groups: (1) 6-h TRE (ad libitum food intake from 1-7 pm, fasting from 7pm-1pm); (2) CR (25% energy restriction daily); or (3) control group (ad libitum intake with no meal timing restrictions).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome, Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
6-hour Time restricted eating (TRE)
Arm Type
Experimental
Arm Description
Ad libitum food intake from 1-7 pm every day Fasting from 7-1 pm every day (18-h fast)
Arm Title
Calorie restriction (CR)
Arm Type
Experimental
Arm Description
25% energy restriction every day
Arm Title
Control
Arm Type
Experimental
Arm Description
Usual diet
Intervention Type
Other
Intervention Name(s)
6-h Time restricted eating (TRE)
Intervention Description
Ad libitum food intake from 1-7 pm every day Fasting from 7-1 pm every day (18-h fast)
Intervention Type
Other
Intervention Name(s)
Calorie restriction (CR)
Intervention Description
25% energy restriction every day
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Usual diet
Primary Outcome Measure Information:
Title
Change in body weight
Description
Measured by an electronic scale
Time Frame
Measured at month 0 and 6
Secondary Outcome Measure Information:
Title
Change in fat mass, lean mass, visceral fat mass
Description
Measured by DXA
Time Frame
Measured at month 0 and 6
Title
Change in bone mineral density
Description
Measured by DXA
Time Frame
Measured at month 0 and 6
Title
Change in waist circumference
Description
Measured by a measuring tape
Time Frame
Measured at month 0 and 6
Title
Change in Insulin sensitivity
Description
Measured by oral glucose tolerance test (OGTT)
Time Frame
Measured at month 0 and 6
Title
Change in Fasting glucose
Description
Measured by a commercial lab (Medstar, IL)
Time Frame
Measured at month 0 and 6
Title
Change in Fasting insulin
Description
Measured by a commercial lab (Medstar, IL)
Time Frame
Measured at month 0 and 6
Title
Change in HbA1c
Description
Measured by a commercial lab (Medstar, IL)
Time Frame
Measured at month 0 and 6
Title
Change in Blood pressure
Description
Measured by a blood pressure cuff
Time Frame
Measured at month 0 and 6
Title
Change in heart rate
Description
Measured by a blood pressure cuff
Time Frame
Measured at month 0 and 6
Title
Change in Plasma lipids (LDL cholesterol, HDL cholesterol, triglycerides)
Description
Measured by a commercial lab (Medstar, IL)
Time Frame
Measured at month 0 and 6
Title
Change in inflammatory markers (TNF-apha, IL-6, IL-10, IL-B, hs-CRP)
Description
Measured by ELISA
Time Frame
Measured at month 0 and 6
Title
Change in oxidative stress (8-isoprostane)
Description
Measured by ELISA
Time Frame
Measured at month 0 and 6
Title
Change in reproductive hormones (testosterone, DHEA, SHBG, androstenedione)
Description
Measured by ELISA
Time Frame
Measured at month 0 and 6
Title
Change in energy and nutrient intake
Description
Measured by 7-day food record
Time Frame
Measured at month 0 and 6
Title
Change in physical activity (steps/d)
Description
Measured by pedometer
Time Frame
Measured at month 0 and 6
Title
Change in mood
Description
Measured by 36-Item Short Form Survey (SF-36), total score 0-100. Higher scores mean worse outcome.
Time Frame
Measured at month 0 and 6
Title
Change in appetite
Description
Measured by Visual analog scale (VAS). Scored from 0-100. Higher score means higher appetite.
Time Frame
Measured at month 0 and 6

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Women with PCOS will be invited to participate in the study.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Krista Varady, PhD
Organizational Affiliation
University of Illinois Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Illinois Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Time Restricted Eating for the Treatment of PCOS

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