TREAT: Study of Time-restricted Eating on Weight Loss.

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT03393195
Collaborator
University of Wisconsin, Madison (Other)
137
1
2
17.4
7.9

Study Details

Study Description

Brief Summary

This is a randomized controlled trial studying the effects of time-restricted eating (TRE) on weight loss in obese humans. Obesity is the number one risk factor for type 2 Diabetes Mellitus (T2DM), and numerous studies demonstrate that weight loss is an effective strategy to prevent T2DM and improve the metabolic health of people diagnosed with T2DM. Unfortunately, classical calorie restriction diets often fail to produce long-term weight loss due to low compliance, reduced resting metabolic rate (RMR), and other factors. Therefore, novel dieting techniques must be explored in order to successfully treat obesity and prevent T2DM. Studies in mice provide compelling evidence that feeding/fasting cycles can be altered to produce beneficial effects on weight loss and metabolic health markers in the absence of calorie restriction. Limited research in human subjects suggests that this feeding paradigm may translate to human health as well, however, more research needs to be done in order to confirm this hypothesis. This study will determine if TRE can lead to weight loss in obese human subjects. Secondary outcomes include changes in body composition, HOMA-IR, hormonal and biochemical serum markers, RMR, and total energy expenditure (TEE).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Time-restricted Eating plan
  • Behavioral: Consistent Meal timing plan
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
137 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This is a randomized controlled trial. Participants will randomly assigned to one of two diet interventions for the duration of the 12-week study.This is a randomized controlled trial. Participants will randomly assigned to one of two diet interventions for the duration of the 12-week study.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Study of Time-restricted Eating on Weight Loss. A Randomized Controlled Trial of the Effects of Time-restricted Eating on Weight Loss in Obese Subjects.
Actual Study Start Date :
Jul 30, 2018
Actual Primary Completion Date :
Oct 23, 2019
Actual Study Completion Date :
Jan 10, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Time-restricted eating plan

Participants in this group will be instructed to fast every day from 8pm until 12pm the following day. From 12pm until 8pm, participants can eat and drink whatever they want. During fasting hours, participants can drink water and black coffee.

Behavioral: Time-restricted Eating plan
Research team will prescribe an eating plan for the participant to follow for the 12 week study. The eating plan will consist of eating during a specified 8 hour window and fasting for the remaining 16 hours of the day.

Active Comparator: Consistent Meal Timing Plan

Participants in this group will be instructed to eat three daily meals during specified eating times. Their first meal will be between 7am-11am. Second meal between 11am and 3pm, and third meal between 4pm-10pm. Participants will be encouraged to eat small snacks if needed so that they can eat their next meal during the specified window.

Behavioral: Consistent Meal timing plan
Research team will prescribe an eating plan for the participant to follow for the 12 week study.The eating plan will consist of eating three structured meals each day during three specified meal windows.

Outcome Measures

Primary Outcome Measures

  1. Weight Loss [Daily for 12 weeks]

    Measure changes in weight during the 12 week study

Secondary Outcome Measures

  1. Fat loss [Measured twice: Once at study start and once 12 weeks later]

    Measure changes in fat mass during the 12 week study using DXA data

  2. Changes in lean mass [Measured twice: Once at study start and once 12 weeks later]

    Measure changes in lean mass during the 12 week study using DXA data

  3. Fasting insulin levels [Measured twice: Once at study start and once 12 weeks later]

    Measure fasting insulin levels pre and post intervention

  4. Resting metabolic rate [Measured twice: Once at study start and once 12 weeks later]

    Will measure participants resting metabolic rate

  5. Total energy expenditure [Measured twice: Once at study start and once 12 weeks later]

    Will measure participants total energy expenditure during the week leading up to the study start and during the final week of the study

  6. Changes in fasting glucose levels [Measured twice: Once at study start and once 12 weeks later]

    WIll measure fasting blood glucose levels prior to diet intervention and again at study completion

  7. Changes in HbA1c levels [Measured twice: Once at study start and once 12 weeks later]

    WIll measure HbA1c levels prior to diet intervention and again at study completion

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • BMI between 30-40 kg/m2

  • Participants must regularly consume breakfast (at least 5 days per week)

  • Must speak, read, and comprehend English

  • Access to reliable internet and/or wifi

  • Must have a valid email address and phone number

  • Must have a cellular phone with data plan

Exclusion Criteria:
  • HIV or immunocompromised

  • Current or past cancer diagnosis

  • Pregnant, breastfeeding, or planned pregnancy in next 6 months

  • Beginning or ending hormonal contraception in next 6 months

  • Current diagnosis of type or type 2 diabetes

  • Currently taking glucose-lowering drugs, statins, or oral steroids

  • History of gastric bypass surgery or any other weight-loss surgery

  • History of anorexia or bulimia

  • Frequent travel across time zones or unusual work hours

  • Unable to fast for prolonged periods due to medical condition

  • Unable to stand for several minutes without aid

  • Cannot lie down on cushioned table for 30 minutes

  • No internal metal artifacts that would alter body composition

  • Unable to travel to UCSF for in-person testing

  • Requires translator services

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCSF Medical Center San Francisco California United States 94143

Sponsors and Collaborators

  • University of California, San Francisco
  • University of Wisconsin, Madison

Investigators

  • Principal Investigator: Ethan J Weiss, MD, University of California, San Francisco

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT03393195
Other Study ID Numbers:
  • 17-22110
First Posted:
Jan 8, 2018
Last Update Posted:
Mar 3, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of California, San Francisco
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 3, 2020