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Clinical Trials/NCT06749951
NCT06749951
Recruiting
Not Applicable

Cognitive Behavioural Therapy for Insomnia in Patients With Coronary Heart Disease: A Randomized Controlled Trial With Six Months Follow-up

Vestre Viken Hospital Trust1 site in 1 country76 target enrollmentDecember 30, 2024

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.

Registry
clinicaltrials.gov
Start Date
December 30, 2024
End Date
June 15, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

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)

Study Sites (1)

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