Circadian Intervention to Improve Cardiometabolic Health

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

Sponsor
University of Utah
Study ID
NCT05943626
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 45 Years
Healthy Volunteers
Accepted

Interventions

  • Circadian Intervention — BEHAVIORAL
    The circadian intervention group will receive counseling and instruction to reduce evening and nighttime light exposure, increase morning room light and sunlight exposure, and to finish all food consumption at least 4 hours before bedtime.

Study Details

The overall goal is to examine the efficacy of a circadian intervention in people with overweight and obesity and habitual short sleep duration (HSSD). Participants will undergo a randomized controlled trial, with circadian intervention and control (healthy lifestyle) groups. The circadian intervention is designed to reduce nighttime light exposure and after-dinner snack food intake. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).

Key Dates

Start date
Jun 13, 2023
Status verified
Dec 2024
Primary completion
Mar 31, 2026
Completion
Mar 31, 2026

Study Design

Enrollment
20 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
    Circadian-based intervention focused on timing of light exposure and food intake.

Primary Outcome Measure

Insulin sensitivity change from baseline [ Time Frame: Change from baseline to end of the ~8 week experimental segment ]

Central Contacts

Locations (1)

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

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