Timing your meals may help maintain weight loss
NCT ID NCT05742165
First seen Jun 27, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This study looked at whether limiting eating to a 6- or 10-hour window each day helps adults who recently lost weight keep it off. 29 participants were randomly assigned to one of two time-restricted eating plans for 12 weeks. The goal was to see if this approach is practical and acceptable for weight loss maintenance.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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29 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Jan 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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NYU Langone Health
New York, New York, 10016, United States
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