Registry of emotional stress in patients undergoing coronary interventions
Official title: Tilburg Health Outcomes Registry of Emotional Stress in Coronary Intervention
Run by Tilburg University · NCT02621216 · Data updated 2026-11-12
This study looks at how emotional stress affects the long-term health of people with heart disease after they have heart procedures.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 3000 (estimated) |
| Sponsor | Tilburg University Academic / other |
| Locations | 1 site (Tilburg, North Brabant) |
| Status | Recruiting |
| Started | December 4, 2013 |
| Main results expected | December 2027 |
| Study ends | December 2037 |
| Registry record updated | April 15, 2024 |
| Trial ID | NCT02621216 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients who have undergone percutaneous coronary intervention and can communicate effectively in Dutch.
✕Probably not a fit
Patients with life-threatening comorbidities or cognitive disorders may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to assess the long-term effects of percutaneous coronary interventions (PCI) on patients with coronary heart disease, focusing on the psychological risk factors that may influence their prognosis. It seeks to understand the interplay between psychological factors and cardiovascular outcomes, as well as the adherence to current treatment guidelines. The study will involve a large real-world clinical sample to gather data on the emotional and psychological well-being of patients post-PCI.
Why it matters
Potential benefit: If successful, this study could lead to improved psychological screening and support for patients undergoing PCI, enhancing their overall health outcomes.
How similar studies have gone: While there is limited long-term follow-up data on the psychological impacts of PCI, the study's approach to examining multiple psychological risk factors is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * PCI * Sufficient understanding of Dutch language Exclusion Criteria: * life threatening comorbidity (e.g., metastasized cancer) * cognitive disorder
Where it's running
-
Elisabeth-TweeSteden hospital
Tilburg, North Brabant, Netherlands Recruiting
Study contacts
- Principal investigator: Nina Kupper, PhD — Tilburg University
- Study coordinator: Nina Kupper, PhD
- Email: h.m.kupper@tilburguniversity.edu
- Phone: +31134662956
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.