- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06438159
Impact of Mindfulness-Based Stress Reduction Meditation Practice on Patients After Cardiac Rehabilitation. (CARDIO-MBSR)
Impact of Mindfulness-Based Stress Reduction Meditation Practice on Medium- and Long-term Follow-up of Cardiac Patients After Cardiac Rehabilitation.
Cardiac rehabilitation is a major component of treatment for patients suffering from coronary pathology revealed by myocardial infarction or acute coronary syndrome warranting transluminal coronary angioplasty, as well as in the aftermath of cardiac surgery.
A significant proportion of patients in this situation (40%) suffer from varying degrees of anxiety and depression, which are difficult to treat. These impair their quality of life and can make it more difficult for them to take part in the rehabilitation program, compromising the results that can be expected. Finally, they are often associated with lax compliance with medical treatment, less control of risk factors and less regular exercise.
Cardiac rehabilitation teams are well aware of this anxiety-depressive picture, and various therapies such as sophrology, relaxation and yoga have been proposed as alternatives to conventional medical treatments to help patients through this period.
Among these alternatives is the concept of "Mindfulness-Based Meditation", based on the Mindfulness-Based Stress Reduction (MBSR) protocol described by Dr. JKabat Zinn.
It has been the subject of several prospective randomized studies, which have demonstrated that it is suitable for the management of patients in this situation, and that it has measurable beneficial effects on their sense of well-being.
To our knowledge, the MBSR program used in cardiac rehabilitation has never been the subject of a randomized comparative study in France to assess its effectiveness on medium- and long-term anxiety-depressive disorders. This is the objective of this study.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Bernard Truong, MD
Study Contact Backup
- Name: Bernard Truong, MD
- Phone Number: 0556003048
- Email: recherche.na@elsan.care
Study Locations
-
-
-
Aressy, France, 64320
- Recruiting
- Clinique d'Aressy
-
Contact:
- Bernard Truong, MD
-
Contact:
- Bernard Truong, MD
- Phone Number: 0556003048
- Email: recherche.na@elsan.care
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Cardiac patients eligible for cardiac rehabilitation,
- 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
- Age ≥ 18 years
- Affiliated with a social security scheme or beneficiary of such a scheme
- Patient signed free and informed consent form
Exclusion Criteria:
- Patients already treated for severe psychiatric disorders (major depression, psychosis, schizophrenia)
- Inability to follow the 8-week MBSR program
- Protected patient: minor, adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
- 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.
- Pregnant or breast-feeding patient
- Refusal to participate in the study or inability to comply with the study protocol for any reason whatsoever
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Cardiac rehabilitation with Mindfulness-Based Stress Reduction (MBSR)
Conventional cardiac rehabilitation over 4 weeks with the introduction of MBSR over 8 weeks
|
The MBSR program is as follows:
|
|
Active Comparator: Conventional cardiac rehabilitation
Conventional cardiac rehabilitation over 4 weeks
|
The usual cardiac rehabilitation program combines exercise training and therapeutic education workshops, with a daily session for four weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline of HADS anxiety and depression scores
Time Frame: Baseline and 12 months
|
HADS (Hospital Anxiety and Depression Scale) is a self questionnaire including 14 items which identifies and quantifies the depression and anxiety from which a person suffers.
|
Baseline and 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To assess the quality of life
Time Frame: Baseline, 1 month, 6 months and 12 months
|
The patients' quality of life will be measured by the MQOL-R questionnaire, which is a 14-point tool forming 4 subscales: physical, psychological, existential and social.
|
Baseline, 1 month, 6 months and 12 months
|
|
Medical treatment compliance
Time Frame: Baseline, 1 month, 6 months and 12 months
|
The patients' compliance to their medical treatment will be measured by the GIRERD self-questionnaire including 6 questions, to assess compliance, i.e. whether treatment is taken regularly and as prescribed.
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "fasting blood glucose"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
fasting blood glucose (in g/L)
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "glycosylated hemoglobin"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
glycosylated hemoglobin (% of total hemoglobin)
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "Lipid profile LDLc"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
Low Density Lipoprotein cholesterol (g/l)
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "Lipid profile HDLc"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
High Density Lipoprotein cholesterol (g/l)
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "BMI"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
BMI ( weight and height will be combined to report BMI in kg/m2)
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "effort"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
6-minute walk test
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "activity"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
Ricci Gagnon scale: self questionnaire including 9 questions to evaluate if the subject has an inactive, active or very active profile
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "Tobacco consumption"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
Tobacco consumption (in packs.year)
|
Baseline, 1 month, 6 months and 12 months
|
|
Changes from baseline of cardiac risk factor "Blood pressure measurement"
Time Frame: Baseline, 1 month, 6 months and 12 months
|
Blood pressure
|
Baseline, 1 month, 6 months and 12 months
|
|
To assess the patient's anxiety
Time Frame: Baseline, 1 months and 6 months
|
HADS anxiety score
|
Baseline, 1 months and 6 months
|
|
To assess the patient's depression
Time Frame: Baseline, 1 months and 6 months
|
HADS depression score
|
Baseline, 1 months and 6 months
|
|
To evaluate the continuation of formal and informal mindfulness meditation practices in patients who have benefited from the MBSR program.
Time Frame: 3 months, 6 months and 12 months
|
Patients of the MBSR group will be asked two questions : "Do you still do formal meditation practices?" "Do you still do informal meditation practices?" |
3 months, 6 months and 12 months
|
|
To evaluate the patient's "mindfulness" and its impact on vital aspects in patients who have benefited from the MBSR program.
Time Frame: 3 months, 6 months and 12 months
|
FFMQ (Five Facets Mindfulness Questionnaire) questionnaire, which includes 39 questions, which assess the 5 facets which constitute mindfulness as a construct:
|
3 months, 6 months and 12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CARDIO-MBSR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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