Cognitive Behavioural Therapy for Insomnia in Patients With Coronary Heart Disease: A Randomized Controlled Trial With Six Months Follow-up
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Insomnia Chronic
- Sponsor
- Vestre Viken Hospital Trust
- Enrollment
- 76
- Locations
- 1
- Primary Endpoint
- Changes in insomnia severity
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
Insomnia is prevalent (45%) in CHD patients and associated with significantly increased risk for recurrent cardiovascular events. Insomnia has recently been identified as the third most important risk factor for prognosis. However, very few insomnia patients are identified and receive treatment of insomnia today. CBT-I is the first-line treatment for insomnia, but studies on the effects in CHD patients are lacking. This project aims to document the effectiveness of Cognitive Behavioural therapy for insomnia (CBT-I) in an outpatient population with coronary heart disease (CHD). Furthermore, the biological and psychological mechanisms that may mediate the effects of the intervention will be identified. Finally, a health-economic simulation and a qualitative study of the participants experiences with CBT-I will be performed. This prospective, randomized, intervention study will continue until data have been collected for the primary outcome on 66 CHD outpatients with a diagnosis of insomnia assessed by Bergen Insomnia Scale (BIS). Participants will be randomised to a short, nurse-administered, CBT-I delivered in a group format or to sleep hygiene advice. The primary outcome will be remission from BIS-insomnia post-treatment and at 6-months follow-up. Secondary outcomes will be changes in insomnia severity, objective and subjective sleep parameters, daytime symptoms of insomnia, and quality of life. Exploratory outcomes include inflammation, cortisol, HbA1C, and cognitions/metacognitions. The project may document the effectiveness of CBT-I for a large patient-group with potentially favorable long-term effects on important clinical outcomes.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Changes in insomnia severity
Time Frame: From baseline to weeks 6-8 and 26
Between- and within- group differences in insomnia severity assessed by the Insomnia Severity Index
Remission clinical diagnosis of insomnia
Time Frame: From baseline to weeks 6-8 and 26
Between- and within- group differences in the proportion witn remission of insomnia diagnosis assessed by the Bergen Insomnia Scale
Secondary Outcomes
- Changes in insomnia assessed by the Pittsburgh Sleep Quality Index(From baseline to weeks 6-8 and 26)
- Changes in subjective sleep efficiency(From baseline to weeks 6-8 and 26)
- Changes in objective sleep efficiency(From baseline to weeks 6-8 and 26)
- Changes in subjective total sleep time(From baseline to weeks 6-8 and 26)
- Changes in objective total sleep time(From baseline to weeks 6-8 and 26)
- Changes in subjective sleep onset latency(From baseline to weeks 6-8 and 26)
- Changes in objective sleep onset latency(From baseline to weeks 6-8 and 26)
- Changes in subjective wake after sleep onset(From baseline to weeks 6-8 and 26)
- Changes in objective wake after sleep onset(From baseline to weeks 6-8 and 26)
- Changes in symptoms of depression and anxiety(From baseline to weeks 6-8 and 26)
- Changes in daytime sleepiness(From baseline to weeks 6-8 and 26)
- Changes in fatigue(From baseline to weeks 6-8 and 26)
- Changes in general quality of life(From baseline to weeks 6-8 and 26)
- Changes in sleep-related quality of life(From baseline to weeks 6-8 and 26)