About this trial

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).

Eligibility criteria

Qualifiers

Age: 18-45 years old; equal numbers of men and women

Body mass index (BMI): 25.0-34.9 kg/m2,

Sleep Habits: habitual self-reported average total sleep time (TST) <6.5 hours per night for prior 6 months

Disqualifiers

Clinically diagnosed sleep disorder or major psychiatric illness

Evidence of significant organ dysfunction or disease (e.g., diagnosed diabetes, cardiovascular disease, or kidney disease)

Use of prescription drugs or substances known to influence sleep or glucose metabolism

Shift-work: current or history of within last year

Trial design

Treatments tested in this trial

  • Circadian Intervention

Treatment groups

20 Participants
are divided into 2 treatment groups

Locations

1
College of Health Research Complex--University of Utah84112, Salt Lake CityUtah, United States

Sponsors and collaborators

University of Utah

Lead sponsor