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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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT04506151). StuddyBuddy aggregates publicly available trial information.