OPTImizing CArdiac REhabilitation by REfining Sleep and STress
Recruiting
N/A
Interventional Study
Cardiovascular Diseases
Cardiac Rehabilitation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 200 (estimated)
- Sponsor
- Erasmus Medical Center · Other
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About This Trial
The primary objective of this project is to investigate the effectiveness and costs of integrating a behavioural program targeting sleep and stress (the RESST intervention) into cardiac rehabilitation (CR). In addition, the investigators will also study whether parameters regarding diversity (e.g., sex, ethnicity, socioeconomic position) are associated with intervention effectiveness. Furthermore,…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Participate in CR at one of the study centres for any cardiac diagnosis or reason as stated in the Dutch guidelines
* Age at or above 18 years
* Proficient in the Dutch language
* Experiencing sleep and/or stress problems as indicated by a high score on the Pittsburgh Sleep Qu…
Contacts