Clinical trial

A Study of Time Restricted Eating in Obese Adults

Active, not recruiting · Not applicable · 1 countries · Registry ID NCT05660291

Active, not recruitingNot applicableInterventional

What this study is about

The purpose of this pilot study is to understand the difference between early and late time-restricted eating on weight and body mass index (BMI), and evaluate the barriers encountered and the effect on quality of life.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 64 Years
SexAll
Healthy volunteersNot accepted
ConditionOverweight

Full registry criteria

Inclusion Criteria: * Ability to read and understand English * BMI ≥ to 25. Exclusion Criteria: * Regularly skip meals. * Are unwilling or unable to limit eating to an 8-hour window. * Have a current Melanoma or cancer diagnosis. * Currently breastfeeding. * Pregnant, or planned to be pregnant within 3 months. * Are taking insulin or sulfonylurea drugs. * Are taking weight loss medications or had weight loss surgery within the last year. * Have a history of eating disorders.

Treatments and study arms

Early time-restricted eating

Behavioral

Subjects can eat whatever they want between the hours of 8:00 AM and 4:00 PM and can only consume water, black coffee/tea, or other zero calorie drinks (artificial sweeteners are okay) outside your designated eating window (from 4:00 PM to 8:00 AM).

Late time-restricted eating

Behavioral

Subjects can eat whatever they want between the hours of 12:00 PM and 8:00 PM and can only consume water, black coffee/tea, or other zero calorie drinks (artificial sweeteners are okay) outside your designated eating window (from 8:00 PM to noon).

Primary outcomes

Change in weightBaseline, 12 weeks

Reported in kilograms (kg)

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Mayo Clinic Minnesota🇺🇸 Rochester, Minnesota, United States