Clinical trial Recruiting at 1 site Interventional Ages 18 to 50 Women only

Mindfulness for Women with Coronary Artery Disease

Official title: THE EFFECT OF A MINDFULNESS-BASED STRESS REDUCTION PROGRAM ON QUALITY OF LIFE , ANXIETY AND EMPOWERMENT LEVELS IN WOMEN WITH CORONARY ARTERY DISEASE

Run by TC Erciyes University · NCT07371806 · Data updated 2026-11-12

This study tests whether a mindfulness-based program helps women with coronary artery disease reduce stress and improve quality of life.

Quick facts

Study typeInterventional
Ages18 Years to 50 Years
SexWomen only
Enrollment70 (estimated)
SponsorTC Erciyes University
Academic / other
Locations1 site (Kayseri, Türki̇ye)
StatusRecruiting
StartedSeptember 1, 2026
Main results expectedJanuary 20, 2027
Study endsMay 20, 2027
Registry record updatedSeptember 11, 2026
Trial IDNCT07371806 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women aged 18-50 with a confirmed diagnosis of CAD for at least one month, baseline anxiety, basic education, an active social network, and willingness to participate in mindfulness sessions.

Probably not a fit

Individuals without significant anxiety or those outside the 18-50 age range may not experience measurable benefits from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study focuses on women with diagnosed coronary artery disease and elevated anxiety. Participants will undergo a mindfulness-based intervention program to see if it can lessen stress and improve emotional well-being. Eligibility includes adults 18-50, ongoing CAD for at least one month, baseline anxiety, and active social support, with exclusions for language/hearing barriers, menopause, and psychiatric disorders. The study is conducted at Kayseri City Hospital in Turkey under the lead sponsor TC Erciyes University. Outcomes will inform whether mindfulness strategies can be effectively tailored for female CAD patients.

Why it matters

Potential benefit: If successful, participants may experience reduced stress and better quality of life related to CAD.

How similar studies have gone: Previous research suggests mindfulness can reduce stress in cardiovascular populations, but sex-specific data in women with CAD are limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosed with coronary artery disease (CAD) for at least 1 month.
* Score of 14 or higher on the Short Form of the State-Trait Anxiety Inventory (STAI-SF) at baseline.
* At least primary school education.
* Age between 18 and 50 years.
* Sexually active.
* Having an active social network.

Exclusion Criteria:

* Individuals with hearing or language impairments that would hinder communication.
* Women who have entered menopause.
* Women with psychiatric disorders.

Discontinuation Criteria:

* Participants who choose to withdraw from the study.
* Participants who miss two intervention sessions.
* Participants with incomplete data on study forms.

Where it's running

  • Kayseri Şehir Hastanesi
    Kayseri, Türki̇ye, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.