Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are taking part in a cardiac rehabilitation (heart recovery) program at one of the study centres, for any heart-related reason covered by Dutch medical guidelines
- People aged 18 or older
- People who are able to read and communicate in Dutch
- People who are experiencing sleep problems or stress, as shown by a score above 5 on a standard sleep quality questionnaire (PSQI) or a score above 13 on a standard stress questionnaire (PSS-10)
- People who have given their written agreement to take part in the study
Who may not be able to join:
- People with serious psychiatric (mental health), cognitive (thinking or memory), or physical conditions that would prevent them from taking part in cardiac rehabilitation
- People who are currently receiving treatment for sleep problems, stress, or any other type of behavioural therapy at the start of the study, or who are expected to begin such treatment within the first 6 months — if that treatment could interfere with the study program. Note: people who have previously been diagnosed with a sleep disorder may still be considered eligible if they are still experiencing sleep or stress problems, unless they fall under the condition above. People using an ongoing treatment (such as a CPAP breathing machine for sleep apnoea) that has kept their sleep and stress stable for the 3 months before their heart event may still be considered eligible (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +31107033190
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Objectively assessed sleep duration; Objectively assessed sleep-onset latency; Objectively assessed wake after sleep onset; Objectively assessed sleep efficiency; Self-reported sleep quality; Perceived stress level
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.