Improving adherence to digital treatment for insomnia with telehealth support
Enhancing Digital CBT-I to Improve Adherence and Reduce Disparities
NA · Henry Ford Health System · NCT05182372
This study is testing if adding telehealth coaching to a digital treatment for insomnia helps people, especially those with lower incomes, stick to their treatment better.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 600 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Henry Ford Health System (other) |
| Locations | 1 site (Novi, Michigan) |
| Trial ID | NCT05182372 on ClinicalTrials.gov |
What this trial studies
This research focuses on enhancing Digital Cognitive Behavioral Treatment for Insomnia (dCBT-I) by incorporating telehealth coaching to improve treatment adherence, particularly among individuals with low socioeconomic status. The study will recruit participants from the Henry Ford Health System and the Medicare/Medicaid data warehouse, screening them for eligibility based on insomnia severity. Participants will be randomized into two groups: one receiving standard dCBT-I and the other receiving dCBT-I with additional telehealth coaching. The study aims to identify behavioral, physical, and sociocultural factors influencing treatment engagement and will include semi-structured interviews to explore barriers and facilitators to adherence.
Who should consider this trial
Good fit: Ideal candidates for this study are adults diagnosed with insomnia who are at risk for treatment non-completion.
Not a fit: Patients under 18 years old or those with untreated severe medical or psychiatric disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve treatment adherence for insomnia, particularly in underserved populations.
How similar studies have performed: Other studies have shown promise in using telehealth interventions to enhance treatment adherence, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Determination of insomnia (ISI \>14) Exclusion Criteria: * Age \< 18 * Unwillingness/inability to participate * Bipolar or Seizure Disorders * Untreated sleep disorders other than insomnia * Untreated and severe medical or psychiatric disorders
Where this trial is running
Novi, Michigan
- Henry Ford Columbus Medical Center — Novi, Michigan, United States (RECRUITING)
Study contacts
- Principal investigator: Philip A Cheng, PhD — Henry Ford Health System
- Study coordinator: Philip Cheng, PhD
- Email: pcheng1@hfhs.org
- Phone: (248)344-7361
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Insomnia, digital CBTI