About this trial

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.

Eligibility criteria

Qualifiers

Age ≥ 22 years and < 80 years of age

Prediabetes

Insomnia

Regular access to device with internet access

Disqualifiers

BMI > 40 kg/m2

Sleep comorbidities detected in medical record or via medical history

Shift work or significant, externally imposed irregular sleep schedule

moderate to severe OSA by home sleep apnea test as part of trial protocol

Trial design

Treatments tested in this trial

  • SHUTi
  • Patient Education

Treatment groups

300 Participants
are divided into 2 treatment groups

Locations

1
Kaiser Permanente Center for Health Research97227, PortlandOregon, United States

Sponsors and collaborators

Kaiser Permanente

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator