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Enhancing Digital CBT-I to Improve Adherence and Reduce Disparities

NCT05182372 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 600

Last updated 2026-04-13

No results posted yet for this study

Summary

The primary objective of this research study is to increase adherence of Digital Cognitive Behavioral Treatment for Insomnia (dCBT-I). Additionally, this study will examine behavioral, physical, and sociocultural factors associated with treatment engagement.

Conditions

Interventions

BEHAVIORAL

Enhanced dCBT-I

Telehealth Coaching

Sponsors & Collaborators

  • University of Michigan

    collaborator OTHER

  • National Jewish Health

    collaborator OTHER

  • Henry Ford Health System

    lead OTHER

Principal Investigators

  • Philip A Cheng, PhD · Henry Ford Health System

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-18
Primary Completion
2026-04-30
Completion
2026-08-30

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05182372 on ClinicalTrials.gov