Diabetes Mellitus, Type 2 Clinical Trial
Official title:
Sleep for Health: A Randomized Clinical Trial Examining the Effects of Cognitive Behavioral Therapy for Insomnia on Diabetes Risk
This study tests whether providing cognitive behavioral therapy for insomnia (CBT-I) to people with prediabetes results in a reduction in glucose levels compared to a patient education control program.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | March 2027 |
Est. primary completion date | December 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 22 Years to 79 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | Kaiser Permanente Center for Health Research | Portland | Oregon |
Lead Sponsor | Collaborator |
---|---|
Kaiser Permanente | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
United States,
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* Note: There are 34 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 2-hour post-load glucose (2hPG) (mg/dL) | 2-hour post-load glucose (mg/dL) | V1 (baseline), V2 (11 weeks after randomization), V3 (33 weeks from randomization) | |
Secondary | Hemoglobin A1c (A1C) (percentage) | Plasma HgB A1C (percentage) | V1 (baseline), V2 (11 weeks after randomization), V3 (33 weeks from randomization) | |
Secondary | Fasting plasma glucose (FPG) (mg/dL) | Fasting plasma glucose levels (mg/dL) | V1 (baseline), V2 (11 weeks after randomization), V3 (33 weeks from randomization) | |
Secondary | Mean glucose on CGM (mg/dL) | Average blood glucose levels throughout CGM wear duration (mg/dL) | V1 (baseline), V2 (11 weeks after randomization), V3 (33 weeks from randomization) | |
Secondary | Insulin resistance score (probability ranking, Calculated using the insulin and C-peptide concentrations converted to pmol/L) | Insulin resistance score - (probability ranking, Calculated using the insulin and C-peptide concentrations converted to pmol/L) | V1 (baseline), V2 (11 weeks after randomization), V3 (33 weeks from randomization) |
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