Circadian Intervention to Improve Cardiometabolic Health
Recruiting
N/A
Interventional Study
Cardiometabolic Syndrome
Type 2 Diabetes
Sleep
Time Restricted Feeding
Lifestyle Factors
Overweight and Obesity
Insulin Sensitivity
Eating Habit
Sleep Hygiene
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 45
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 20 (estimated)
- Sponsor
- University of Utah · Other
Who this trial is looking for
This trial is looking for men and women between the ages of 18 and 45 who are a bit overweight and have been getting less than 6.5 hours of sleep on average each night. They'll need to be generally healthy, so people with serious health issues or those taking certain medications won’t be able to join. If you're pregnant or recently had a big weight change, this study won't be right for you either.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your Eligibility
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
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
Exclusion Criteria:
1. Clinically diagnosed sleep disorder or majo…
Contacts