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Completed
NCT04506151
Sleep Optimization to Improve Glycemic Control in Adults With Type 1 Diabetes
Conditions: Type 1 Diabetes
Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Phase: NA
Enrollment: 144
Sponsor: University of Illinois at Chicago
Location: University of Illinois Chicago Chicago Illinois
Summary
Up to 40% of adults with type 1 diabetes have insufficient sleep which is associated with negative health consequences including poor blood glucose control and greater diabetes complications. In this study, a sleep intervention (Sleep-Opt) that uses wearable sleep tracking technology, telephone coaching and informational content designed to improve sleep and glycemic control in working-age adults with type 1 diabetes. Sleep-Opt could lead to reduced development of diabetes complications and improve quality of life for adults with type 1 diabetes.
Eligibility Criteria
Inclusion Criteria:
* adults aged 18-65 years
* clinical diagnosis of type 1 diabetes minimum of one year
* reported habitual sleep variability (1 hour/week or more) or sleep duration less than 6.5 hrs/night during work- or weekdays (confirmed with actigraphy sleep watch)
* a desire to improve sleep
* own a smartphone
Exclusion Criteria:
* insomnia symptoms
* at high risk for obstructive sleep apnea
* severe hypoglycemia episode in the past 6 months (e.g. loss of consciousness)
* A1C greater than 10%
* rotating shift or night shift work
* use of sleep medications/aids
* renal impairment (estimated glomerular filtration rate \< 45 ml/min)
* significant current medical morbidities (such as heart failure, cirrhosis, chronic obstructive pulmonary disease requiring oxygen, active treatment for cancer, depression, history of stroke with neurological deficits
* breast feeding, pregnant, or planning pregnancy
Source: ClinicalTrials.gov (NCT04506151). StuddyBuddy aggregates publicly available trial information.