Sleep for Health Study on the Effects of Cognitive Behavioral Therapy for Insomnia on Diabetes Risk
Diabetes Mellitus, Type 2, Prediabetic State, Sleep Initiation and Maintenance Disorders
About this trial
This is an interventional treatment trial for Diabetes Mellitus, Type 2
Eligibility Criteria
Inclusion Criteria: Age ≥ 22 years and < 80 years of age Prediabetes Insomnia Regular access to device with internet access Adequate data at baseline Exclusion Criteria: BMI > 40 kg/m2 Sleep comorbidities detected in medical record or via medical history Shift work or significant, externally imposed irregular sleep schedule OSA by home sleep apnea test as part of trial protocol Received a full course of CBT-I in the last 12 months Current use of medication with glycemic effects: History of type 1 or type 2 diabetes or recent/planned use of hypoglycemic agents (e.g., metformin, insulin) Recent history of bariatric surgery or planning bariatric surgery in the next year Current or recent use of weight loss meds Unstable sleep medication regimen (recent change to schedule or dosage) Significant comorbidity that may interfere with CBT-I uptake or increase risks Unwilling or unable to limit heavy machinery use/long bouts of driving or unstable illness that would be worsened by sleep restriction High risk of falls Epilepsy Medical conditions that interfere with dCBT-I or contribute to insomnia or diabetes risk (e.g., hyperthyroidism, significant kidney disease, active cancer treatment, any medical condition that requires chronic steroid use) Significant alcohol or substance use disorder Active or recent history of eating disorder, recent weight change of >10% Women: pregnancy (current or planned), breastfeeding, < 1 year postpartum Use of hydroxyurea Extensive skin changes or adhesive allergy making CGM sensor use problematic
Sites / Locations
- Kaiser Permanente Center for Health ResearchRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Digital cognitive behavioral therapy (dCBT-I)
Patient Education (PE)
CBT-I is designed to change sleep habits and scheduling factors that affect sleep, and to address misconceptions about sleep and insomnia that perpetuate sleep difficulties. The investigators will employ SHUTi, which is an extensively studied dCBT-I program. SHUTi is intended to improve insomnia symptoms by providing neurobehavioral intervention (cognitive behavioral therapy for insomnia - CBT-I) in adults with chronic insomnia. It is a six-core internet-delivered CBT-I web-based app that is run through a browser. It is accessible via iPhone/iPad, Android phone/tablet, computer or laptop (any device with a browser). SHUTi follows evidence-based CBT-I principles.
Participants will be given access to a patient education website. It will provide nontailored material about insomnia symptoms; the impact, prevalence, and causes of insomnia; and basic lifestyle, environmental, and behavioral strategies to improve sleep.