Circadian Intervention to Improve Cardiometabolic Health
Eligible age
18–45 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
Yes
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
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).
Sponsor: University of Utah
You may qualify if…
- ✓ 1. Age: 18-45 years old; equal numbers of men and women
- ✓ 2. Body mass index (BMI): 25.0-34.9 kg/m2,
- ✓ 3. Sleep Habits: habitual self-reported average total sleep time (TST) \<6.5 hours per night for prior 6 months
You may not qualify if…
- ✕ 1. Clinically diagnosed sleep disorder or major psychiatric illness
- ✕ 2. Evidence of significant organ dysfunction or disease (e.g., diagnosed diabetes, cardiovascular disease, or kidney disease)
- ✕ 3. Use of prescription drugs or substances known to influence sleep or glucose metabolism
- ✕ 4. Shift-work: current or history of within last year
- ✕ 5. Weight change: \>10% of body weight over prior six months
- ✕ 6. Experiencing menopause or post-menopausal
- ✕ 7. Current enrollment in weight loss or physical activity program like the Diabetes Prevention Program
- ✕ 8. Currently pregnant or planning to become pregnant, or currently lactating.
Where it's recruiting
Salt Lake City
Source: ClinicalTrials.gov · NCT05943626 · last updated 2024-12-20