Behavioral therapy for insomnia in older adults
A Quasi-experimental Study Design of Evaluation the Effects of Brief Behavioral Therapy for Insomnia on Regulating Stress and Sleep Quality in Middle-aged and Older Adults With Chronic Insomnia
This study is testing a four-week therapy program to help middle-aged and older adults with chronic insomnia feel better and reduce their stress.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 40 Years and up |
| Sex | All |
| Sponsor | National Cheng-Kung University Hospital Academic / other |
| Locations | 1 site (Tainan City) |
| Trial ID | NCT06073990 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of a four-week Brief Behavioral Therapy for Insomnia (BBTi) program aimed at improving chronic insomnia and reducing stress in middle-aged and older adults. It employs a single-group pre-test and post-test design, recruiting 80 participants who will receive a structured intervention including sleep assessments, education on sleep hygiene, and follow-up evaluations. The program includes face-to-face and telephone interactions to monitor progress and provide necessary adjustments to treatment. Participants must be referred by sleep specialists and meet specific inclusion criteria.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 40 years and older who experience sleep disturbances and are willing to participate.
Not a fit: Patients with cognitive impairment will not benefit from this study as they are excluded from participation.
Why it matters
Potential benefit: If successful, this intervention could significantly improve sleep quality and overall well-being for middle-aged and older adults suffering from chronic insomnia.
How similar studies have performed: Previous studies have shown that behavioral therapies for insomnia can be effective, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * individuals aged 40 years and above, * experiencing sleep disturbances, * willing to participate in the research project and provide informed consent Exclusion Criteria: ●Cognitive impairment
Where this trial is running
Tainan City
- National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University — Tainan City, Taiwan (Recruiting)
Study contacts
- Study coordinator: Yen-Chin Chen
- Email: yenchin2427@gmail.com
- Phone: +886-6-2353535
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.