Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05182372

Enhancing Digital CBT-I to Improve Adherence and Reduce Disparities

Led by Henry Ford Health System · Updated on 2026-04-13

600

Participants Needed

1

Research Sites

223 weeks

Total Duration

On this page

Sponsors

H

Henry Ford Health System

Lead Sponsor

U

University of Michigan

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

Enhancing Digital CBT-I to Improve Adherence and Reduce Disparities

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Determination of insomnia (ISI >14)
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Unwillingness or inability to participate
  • Bipolar or seizure disorders
  • Untreated sleep disorders other than insomnia
  • Untreated and severe medical or psychiatric disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Henry Ford Columbus Medical Center

Novi, Michigan, United States, 48377

Actively Recruiting

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Research Team

P

Philip Cheng, PhD

CONTACT

M

Marleigh Treger, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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