Time Restricted Eating for Weight Loss Maintenance

Not Applicable

Completed

• Conditions: Obesity
• Interventions: Behavioral: Time Restricted Eating (TRE)

• Registration Number: NCT05742165
• Lead Sponsor: NYU Langone Health

Brief Summary

The aim of this pilot feasibility and acceptability, randomized clinical trial will be to examine the effects of two-time restricted eating (TRE) interventions on weight loss maintenance (WLM). This study will be conducted in 40 individuals with non-surgical weight loss of ≥5% initial body weight recruited from the NYU Langone Health Weight Management Program and NY-MOVE! Weight Management Clinic at the Manhattan VA. Measurements will occur at baseline, 4 and 12 weeks. Participants will be randomized with equal allocation to 2 groups: (1) TRE6 or (2) TRE10. The TRE6 will restrict their eating window to 6 hours per day and the TRE10 to 10 hours per day.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2023-02-15
• Study First Submitted QC: 2023-02-15
• Study First Posted: 2023-02-23
• Study Start: 2023-07-17
• Status Verified: 2025-01
• Primary Completion: 2025-01-06
• Study Completion: 2025-01-06
• Last Update Submitted: 2025-01-14
• Last Update Posted: 2025-01-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 29

Inclusion Criteria

• ≥5% non-surgical weight loss from NYULH-WMP and NY-MOVE! Endocrinology Weight Management Clinic in the last 3 months
• BMI between 20.5 - 45 m/kg2
• between the ages 25 to 65 years old
• own a smartphone or willing to use a smartphone if provided for self-monitoring
• Eating window >12 h per day
• <150 mins/wk of physical activity
• log at least 2 meals into the smartphone app on ≥5 days

Exclusion Criteria

• <25 years or >65 years of age
• Body weight in excess of 400lbs (181.4kg)
• pregnant, trying to get pregnant or breastfeeding
• previous or planned bariatric surgery
• previous or current history of eating disorder
• ongoing participation in another weight-management research study
• continued participation in a weight loss program other than the proposed study
• currently on appetite suppressants
• currently following intermittent fasting or skipping meals
• eating window <11h 59min/day
• perform overnight shift work more than once a week
• work that includes travel across one or more time zones
• currently on anti-obesity medications (AOMs) such as, GLP-1 analogues (exenatide, tirzepatide, semaglutide, liraglutide) and pancreatic lipase inhibitors (Orlistat/Xenical and Alli)
• prescribed medications expected to result in weight loss such as Orlistat, Naltrexone, Bupropion, Lorcaserin, Phentermine, Topiramate, or Liraglutide, and who are unwilling to delay treatment with these medications for the next 3 months
• unable or unwilling to provide informed consent
• unable to participate meaningfully in the intervention (e.g., uncorrected sight and hearing impairment)
• unwilling to accept randomization assignment
• unable to log at least 2 meals into the smartphone app on ≥5 d during the screening period
• have type 1 or other conditions that would preclude restricted eating windows
• have type 2 diabetes with a HbA1c >7.0% on medications except for metformin alone
• narcolepsy
• active cancer
• organ dysfunction
• current steroid use
• daytime sleepiness with the Epworth Sleepiness Scale >10
• severe insomnia with a score ≥15 on the Insomnia Severity Index
• >2.5 kg additional weight loss during run-in phase (weight regain is not an exclusion criteria)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Time-Restricted Eating - 10 Hours (TRE10)	Time Restricted Eating (TRE)	Participants will be instructed to consume all daily food and beverages during their allotted 10-hour time period.
Time-Restricted Eating - 6 Hours (TRE6)	Time Restricted Eating (TRE)	Participants will be instructed to consume all daily food and beverages during their allotted 6-hour time period.

Primary Outcome Measures

Name	Time	Method
Recruitment Rate	Up to Week 12	Number of individuals who must be approached to enroll one participant in the study. A recruitment funnel will be developed by documenting the total number of eligible patients completing the NYU Langone Health-WMP and NY- MOVE! programs losing ≥5% of their baseline body weight.
Adherence Rate	Up to Week 12	Using data from participant-worn ActiGraphs and on eating patterns, a day will be labeled "adherent" if all eating occasions (food or beverage with caloric value) are measured inside (± 30 minutes) their prescribed eating window. Adherence rate will be calculated by dividing the total number of adherent days by the total number of days with a logged eating occasion.
Retention Rate	Up to Week 12	Percentage of participants who complete all study visits. Measure of feasibility.
TRE Experience Questionnaire (TRE-EQ) Score	Week 12	Online questionnaire that includes 5-point scaled items (0=strongly disagree, 5=strongly agree) regarding difficulties encountered with hunger and appetite; eating within the assigned window; coordinating the TRE window with work, school and home demands; and accommodating social connections (e.g., behaviors and preferences of fellow diners).

Secondary Outcome Measures

Name	Time	Method
Change from Baseline in Lean Mass	Baseline, Week 12	Measured using Bioelectrical Impedance Analysis (BIA). Expressed in kilograms.
Change from Baseline in Fat Mass	Baseline, Week 12	Measured using BIA. Expressed in kilograms.

Trial Locations

Locations (1)

NYU Langone Health; 🇺🇸 New York, New York, United States