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Study of Time-restricted Eating on Weight Loss. (TREAT)

Primary Purpose

Obesity, Insulin Resistance

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Time-restricted Eating plan
Consistent Meal timing plan
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Weight loss, Diet, Time-restricted feeding

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • UCSF Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Time-restricted eating plan

Consistent Meal Timing Plan

Arm Description

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.

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.

Outcomes

Primary Outcome Measures

Weight Loss
Measure changes in weight during the 12 week study

Secondary Outcome Measures

Fat loss
Measure changes in fat mass during the 12 week study using DXA data
Changes in lean mass
Measure changes in lean mass during the 12 week study using DXA data
Fasting insulin levels
Measure fasting insulin levels pre and post intervention
Resting metabolic rate
Will measure participants resting metabolic rate
Total energy expenditure
Will measure participants total energy expenditure during the week leading up to the study start and during the final week of the study
Changes in fasting glucose levels
WIll measure fasting blood glucose levels prior to diet intervention and again at study completion
Changes in HbA1c levels
WIll measure HbA1c levels prior to diet intervention and again at study completion

Full Information

First Posted
December 20, 2017
Last Updated
February 28, 2020
Sponsor
University of California, San Francisco
Collaborators
University of Wisconsin, Madison
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1. Study Identification

Unique Protocol Identification Number
NCT03393195
Brief Title
Study of Time-restricted Eating on Weight Loss.
Acronym
TREAT
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.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
July 30, 2018 (Actual)
Primary Completion Date
October 23, 2019 (Actual)
Study Completion Date
January 10, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
University of Wisconsin, Madison

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
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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Insulin Resistance
Keywords
Weight loss, Diet, Time-restricted feeding

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
137 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Time-restricted eating plan
Arm Type
Experimental
Arm Description
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.
Arm Title
Consistent Meal Timing Plan
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Time-restricted Eating plan
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Consistent Meal timing plan
Intervention Description
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.
Primary Outcome Measure Information:
Title
Weight Loss
Description
Measure changes in weight during the 12 week study
Time Frame
Daily for 12 weeks
Secondary Outcome Measure Information:
Title
Fat loss
Description
Measure changes in fat mass during the 12 week study using DXA data
Time Frame
Measured twice: Once at study start and once 12 weeks later
Title
Changes in lean mass
Description
Measure changes in lean mass during the 12 week study using DXA data
Time Frame
Measured twice: Once at study start and once 12 weeks later
Title
Fasting insulin levels
Description
Measure fasting insulin levels pre and post intervention
Time Frame
Measured twice: Once at study start and once 12 weeks later
Title
Resting metabolic rate
Description
Will measure participants resting metabolic rate
Time Frame
Measured twice: Once at study start and once 12 weeks later
Title
Total energy expenditure
Description
Will measure participants total energy expenditure during the week leading up to the study start and during the final week of the study
Time Frame
Measured twice: Once at study start and once 12 weeks later
Title
Changes in fasting glucose levels
Description
WIll measure fasting blood glucose levels prior to diet intervention and again at study completion
Time Frame
Measured twice: Once at study start and once 12 weeks later
Title
Changes in HbA1c levels
Description
WIll measure HbA1c levels prior to diet intervention and again at study completion
Time Frame
Measured twice: Once at study start and once 12 weeks later

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ethan J Weiss, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCSF Medical Center
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32986097
Citation
Lowe DA, Wu N, Rohdin-Bibby L, Moore AH, Kelly N, Liu YE, Philip E, Vittinghoff E, Heymsfield SB, Olgin JE, Shepherd JA, Weiss EJ. Effects of Time-Restricted Eating on Weight Loss and Other Metabolic Parameters in Women and Men With Overweight and Obesity: The TREAT Randomized Clinical Trial. JAMA Intern Med. 2020 Nov 1;180(11):1491-1499. doi: 10.1001/jamainternmed.2020.4153. Erratum In: JAMA Intern Med. 2020 Nov 1;180(11):1555. JAMA Intern Med. 2021 Jun 1;181(6):883.
Results Reference
derived

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Study of Time-restricted Eating on Weight Loss.

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