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临床试验/NCT06438159
NCT06438159进行中(未招募)不适用

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

Elsan2 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2024年11月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
74
试验地点
2
主要终点
Change from baseline of HADS anxiety and depression scores

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Cardiac rehabilitation with Mindfulness-Based Stress Reduction (MBSR)

Experimental

Conventional cardiac rehabilitation over 4 weeks with the introduction of MBSR over 8 weeks

干预措施: Cardiac rehabilitation with Mindfulness-Based Stress Reduction (MBSR) (Other)

Conventional cardiac rehabilitation

Active Comparator

Conventional cardiac rehabilitation over 4 weeks

干预措施: Conventional cardiac rehabilitation (Other)

结局指标

主要结局

Change from baseline of HADS anxiety and depression scores

时间窗: 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.

次要结局

  • To assess the quality of life(Baseline, 1 month, 6 months and 12 months)
  • Medical treatment compliance(Baseline, 1 month, 6 months and 12 months)
  • Changes from baseline of cardiac risk factor "activity"(Baseline, 1 month, 6 months and 12 months)
  • Changes from baseline of cardiac risk factor "Tobacco consumption"(Baseline, 1 month, 6 months and 12 months)
  • To assess the patient's depression(Baseline, 1 months and 6 months)
  • Changes from baseline of cardiac risk factor "fasting blood glucose"(Baseline, 1 month, 6 months and 12 months)
  • Changes from baseline of cardiac risk factor "glycosylated hemoglobin"(Baseline, 1 month, 6 months and 12 months)
  • Changes from baseline of cardiac risk factor "Lipid profile HDLc"(Baseline, 1 month, 6 months and 12 months)
  • Changes from baseline of cardiac risk factor "BMI"(Baseline, 1 month, 6 months and 12 months)
  • Changes from baseline of cardiac risk factor "effort"(Baseline, 1 month, 6 months and 12 months)
  • To assess the patient's anxiety(Baseline, 1 months and 6 months)
  • Changes from baseline of cardiac risk factor "Lipid profile LDLc"(Baseline, 1 month, 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.(3 months, 6 months and 12 months)
  • Changes from baseline of cardiac risk factor "Blood pressure measurement"(Baseline, 1 month, 6 months and 12 months)
  • To evaluate the continuation of formal and informal mindfulness meditation practices in patients who have benefited from the MBSR program.(3 months, 6 months and 12 months)

研究者

发起方
Elsan
申办方类型
Other
责任方
Sponsor

研究点 (2)

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