Mindfulness meditation for patients after heart rehabilitation

Impact of Mindfulness-Based Stress Reduction Meditation Practice on Medium- and Long-term Follow-up of Cardiac Patients After Cardiac Rehabilitation.

NA · Elsan · NCT06438159

This study tests if mindfulness meditation can help heart patients feel less anxious and depressed while they go through cardiac rehabilitation.

Quick facts

PhaseNA
Study typeInterventional
Enrollment74 (estimated)
Ages18 Years and up
SexAll
SponsorElsan (other)
Locations1 site (Aressy)
Trial IDNCT06438159 on ClinicalTrials.gov

What this trial studies

This study investigates the effects of Mindfulness-Based Stress Reduction (MBSR) meditation on patients undergoing cardiac rehabilitation. It aims to address the anxiety and depression that many cardiac patients experience, which can hinder their recovery and adherence to treatment. Participants will engage in an 8-week MBSR program alongside conventional cardiac rehabilitation to evaluate improvements in their mental health and overall rehabilitation outcomes.

Who should consider this trial

Good fit: Ideal candidates are cardiac patients eligible for rehabilitation who exhibit moderate anxiety or depression.

Not a fit: Patients with severe psychiatric disorders or those unable to participate in the MBSR program may not benefit from this study.

Why it matters

Potential benefit: If successful, this approach could significantly enhance the mental well-being and recovery of cardiac patients, leading to better rehabilitation outcomes.

How similar studies have performed: Previous studies have shown promising results for mindfulness interventions in improving mental health outcomes in various patient populations, suggesting potential success for this approach.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Cardiac patients eligible for cardiac rehabilitation,
2. Patient with a Hospital Anxiety and Depression Scale (HADS) score for the anxiety dimension (HADS-A) \>7 or a score for the depression dimension (HADS-D) \> 7
3. Age ≥ 18 years
4. Affiliated with a social security scheme or beneficiary of such a scheme
5. Patient signed free and informed consent form

Exclusion Criteria:

1. Patients already treated for severe psychiatric disorders (major depression, psychosis, schizophrenia)
2. Inability to follow the 8-week MBSR program
3. Protected patient: minor, adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
4. Medical conditions which may interfere with the conduct of the study and the investigator's judgment, and which may render the patient unfit to participate in the study.
5. Pregnant or breast-feeding patient
6. Refusal to participate in the study or inability to comply with the study protocol for any reason whatsoever

Where this trial is running

Aressy

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Cardiac Disease, cardiac rehabilitation, MBSR

Last reviewed 2026-05-15 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.