Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
100 participants
INTERVENTIONAL
2023-02-24
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Early time-restricted eating
Subjects window for eating would be between 08:00 AM - 4:00 PM
Early time-restricted eating
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
Subjects window for eating would be between 12:00 PM (noon) and 8:00 PM
Late time-restricted eating
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).
Interventions
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Early time-restricted eating
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
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).
Eligibility Criteria
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Inclusion Criteria
* BMI ≥ to 25.
Exclusion Criteria
* 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.
18 Years
64 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Bradley A. Bohn
Principal Investigator
Principal Investigators
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Bradley Bohn, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic Minnesota
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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22-010547
Identifier Type: -
Identifier Source: org_study_id
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