Enhancing Digital CBT-I to Improve Adherence and Reduce Disparities

Description

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

Insomnia

Study Overview

Study Details

Study overview

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.

Enhancing Digital CBT-I to Improve Adherence and Reduce Disparities

Enhancing Digital CBT-I to Improve Adherence and Reduce Disparities

Condition
Insomnia
Intervention / Treatment

-

Contacts and Locations

Novi

Henry Ford Columbus Medical Center, Novi, Michigan, United States, 48377

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Determination of insomnia (ISI \>14)
  • * Age \< 18
  • * Unwillingness/inability to participate
  • * Bipolar or Seizure Disorders
  • * Untreated sleep disorders other than insomnia
  • * Untreated and severe medical or psychiatric disorders

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Henry Ford Health System,

Philip A Cheng, PhD, PRINCIPAL_INVESTIGATOR, Henry Ford Health System

Study Record Dates

2026-08-30