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

Part of paid clinical trials in Salt Lake City, Utah.

Sponsor
University of Utah
Study ID
NCT06180837
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 45 Years
Healthy Volunteers
Accepted

Interventions

  • Sleep Extension Intervention — BEHAVIORAL
    Sleep extension-based intervention focused on increasing time spent in bed by 2 hours per night by directly scheduling assigned bed and waketimes based on participant's individual schedules. Participants will receive weekly sleep tips and counseling on improving their sleep duration.

Study Details

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).

Key Dates

Start date
Feb 12, 2024
Status verified
Dec 2024
Primary completion
Jan 31, 2028
Completion
Jan 31, 2028

Study Design

Enrollment
70 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • No Intervention: Control Group
    Provided with general health information on diet and physical activity.
  • Experimental: Intervention Group
    Sleep extension-based intervention focused on increasing time in bed by 2 hours per night.

Primary Outcome Measure

Total Plasma Ceramides [ Time Frame: Immediately after the intervention ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
College of Health Research Complex--University of UtahSalt Lake CityUtah84112
Christopher Depner
8015812275

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