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