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NCT07633132Completed

Mind-Body Interventions in Coronary Artery Disease

Effects of Combined Mind-Body Interventions in Patients With Coronary Artery Disease

Source: ClinicalTrials.gov · Last updated 16 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
3 Jun 2026
Start date
9 Jun 2026
Primary completion date
4 Sept 2026
Lead sponsor
şeyda candeniz
NCT number
NCT07633132

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 9 Jun 2026 to the primary completion date, 4 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous regular participation in mind-body interventions such as progressive muscle relaxation, guided imagery, meditation, or similar programs

Other illness

  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ufuk University Faculty of Medicine, Department of Cardiology
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.