Clinical Trial

Effect of Sleep Extension on Ceramides in People With Overweight and Obesity

Recruiting
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Summary
The overall goal is to determine how a sleep extension intervention (increasing time in bed) in individuals who maintain less than 6.5 hours sleep per night affects their plasma ceramides and insulin sensitivity. Participants will undergo a randomized controlled trial, with sleep extension (intervention) and healthy lifestyle (control) groups. The sleep extension is designed to increase participant's time in bed by 2 hours per night. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).
Protocol Amendment History 1 change
minor Completion pushed: 2028-01 -> 2028-05 2026-08-06
Trial Details
NCT Number NCT06180837
Lead Sponsor University of Utah
Conditions Lifestyle Factors, Overweight and Obesity, Insulin Sensitivity, Eating Habit, Sleep Hygiene, Type 2 Diabetes, Sleep, Sleep Deprivation +1 more
Enrollment 70 participants
Start Date 2024-02-12
Primary Completion 2028-01 (estimated)
Study Completion 2028-05 (estimated)
Updated on ClinicalTrials.gov 2026-08-05