Mind-Body Interventions in Coronary Artery Disease
Turkey (Türkiye)40 participantsStarted 2026-06-09
Plain-language summary
This randomized controlled study aims to evaluate the effects of a combined mind-body intervention consisting of progressive muscle relaxation and guided imagery on psychological outcomes in patients with stable coronary artery disease.
A total of 40 participants will be randomly assigned to either an intervention group or a control group. The intervention group will receive eight individualized sessions over four weeks in addition to standard medical care, while the control group will continue with standard care only.
Primary and secondary outcomes will be assessed using validated self-report instruments, including the Perceived Stress Scale (PSS), Hospital Anxiety and Depression Scale (HADS), and COPE Inventory, administered at baseline and after the intervention period.
The main objective of the study is to determine whether structured mind-body techniques can reduce perceived stress, anxiety, and depressive symptoms and improve coping strategies in patients with coronary artery disease.
Who can participate
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Diagnosed with stable coronary artery disease
* Aged between 18 and 65 years
* Able to read and understand Turkish
* Able to complete study questionnaires and assessments
* Willing to provide written informed consent
Exclusion Criteria:
* History of acute coronary syndrome within the last 3 months
* Presence of a diagnosed severe psychiatric disorder
* Cognitive impairment or communication difficulties that may interfere with study participation
* Previous regular participation in mind-body interventions such as progressive muscle relaxation, guided imagery, meditation, or similar programs
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial focuses on mind-body interventions for coronary artery disease and measures changes in perceived stress levels — how confident are you that reducing psychological stress could meaningfully improve my heart health outcomes, and is there evidence to support this approach for someone in my situation?
2Since this trial is listed as 'not yet recruiting,' do you know when it's expected to open, and would it make more sense for me to pursue standard CAD treatments now rather than waiting to see if I qualify?
3The trial is listed as Phase NA, which often means it's not testing a drug but rather a behavioral or psychological approach — can you help me understand what kinds of mind-body interventions might be involved, and whether any risks or commitments come with participating?
4How does the Perceived Stress Scale work as a primary outcome measure, and does focusing on stress reduction alone tell us enough about how this intervention might affect my heart disease specifically?
5Are there already established stress-reduction programs — like cardiac rehabilitation or mindfulness-based therapies — that I could access right now, and how would those compare to what this trial might offer?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.