Myocardial Infarction Clinical Trial
Official title:
Baduanjin Exercise Prevents Post-Myocardial Infarction Left Ventricular Remodeling (BE-PREMIER Trial)
Left ventricular (LV) remodeling following myocardial infarction (MI) is an established prognostic factor for adverse cardiovascular events and the leading cause of heart failure. Empirical observations suggests that Baduanjin exercise, an important component of traditional Chinese Qigong, exert potential impacts on cardiopulmonary function. However, the impact of a Baduanjin exercise-based cardiac rehabilitation program for patients recovering from recent MI has yet to be assessed. The aim of this trail is to evaluate whether Baduanjin exercise would prevent the maladaptive progression to adverse LV remodeling in patients following MI.
Status | Not yet recruiting |
Enrollment | 110 |
Est. completion date | December 2018 |
Est. primary completion date | July 2017 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: 1. Presence of MI who has successful revascularization after the symptom onset; 2. Aged 18 years or over and under 80 years; 3. Availability to attend sessions twice a week over a 12-week period; 4. Physical aptitude to participate in a Baduanjin exercise -based cardiac rehabilitation program. Exclusion Criteria: 1. Inability or difficulty to exercise 2. Prior history of practicing Qigong (Taiji or Baduanjin exercise, etc); 3. Presence of unstable angina, detectable myocardial ischemia (at rest or on exertion), significant valvular disease, and hypertrophic cardiomyopathy; 4. Severe symptomatic congestive heart failure (NYHA cardiac function class IV or left ventricular ejection fraction=35%); 5. Severe pulmonary disease, musculoskeletal system diseases, other comorbidities precluding physical activity; 6. Life-threatening diseases with limited life expectancy <1 year; 7. Pregnant and lactating women; 8. Participation in other clinical trials. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
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Guangdong Provincial Hospital of Traditional Chinese Medicine |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | the percentage change from baseline to 6 months (%?) in echocardiographic LV end-diastolic volume index (LVEDVi) | the percentage change end-diastolic volume index (%) | baseline and 6 months | No |
Secondary | the change in echocardiographic measures of ventricular volumes (LV end-systolic/ diastolic volume) | LV end-systolic/ diastolic volume (mL) | baseline and 6 months | No |
Secondary | The occurrence and composite of major adverse cardiac events (MACE) | defined as cardiogenic death, stroke, recurrent myocardial infarction, readmission on account of deterioration of congestive heart failure or unstable angina, target vessel revascularization | baseline and 6 months | No |
Secondary | MacNew heart disease health-related quality of life questionnaire | in Units on a Scale | baseline and 6 months | No |
Secondary | The short form 36 questionnaire | in Units on a Scale | baseline and 6 months | No |
Secondary | The 6-minute walk test | A 6-minute walk test measures the distance patients can quickly walk in 6 minutes. (in meters) | from 3 to 6 months | No |
Secondary | cardiopulmonary exercise test | from 3 to 6 months | Yes |
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