Women's Lifestyle Balance Study
Completed · Not applicable
Conditions studied: PreDiabetes, Metabolic Syndrome, Overweight
In brief
This pilot study aims to determine whether adding a sleep extension and sleep hygiene intervention to an existing lifestyle improvement program improves its efficacy for weight loss in those at risk for diabetes and cardiovascular disease. Half of the participants will receive the Centers for Disease Control's standard PreventT2 program and half of the participants will receive the same program with an additional sleep intervention.
Key facts
- Study ID
- NCT03184337
- Run by
- University of California, San Francisco
- People needed
- 26
- Starts
- 2017-04-24
- Expected to finish
- 2017-12-31
- Last updated by the study team
- 2018-10-25
Who can join
Age: 30 and older, up to 70. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female (or self-identify as female)
- Age 30-70 years
- BMI 25-38 (or 23-38 if Asian or other Pacific Islander)
- Time in bed <= 7 hours on a typical weeknight
- Meets diagnostic criteria for prediabetes and/or metabolic syndrome
You may not qualify if…
- No regular access to telephone or email (for maintaining contact);
- No access to smartphone, tablet, or laptop computer (for using Fitbit);
- Having a condition that limits physical activity, such as brisk walking;
- Having a diagnosis of type 1 or type 2 diabetes or been previously treated with diabetes medications;
- Having a cardiac event or cardiac surgery in the past year;
- Having a metabolic condition that prevents weight loss;
- Working night shift (Midnight - 4 AM)
- Inability to complete the baseline assessment (REDCap survey and Fitbit tracking of activity, diet, and sleep for 7 days)
Where it is running
- University of California, San Francisco — San Francisco, California, United States
Full record on ClinicalTrials.gov
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