Efficacy and safety of Tai Chi for rehabilitation after PCI in patients with coronary heart disease: A protocol of a randomized controlled trial
- Registration Number
- TCTR20230101002
- Lead Sponsor
- Huaying Wang
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- All
- Target Recruitment
- 68
(1) Meet the diagnosis of angina pectoris in CHD, and meet coronary angiography or coronary angiography showed at least one coronary artery stenosis and catheter stenosis no less than 50%, cardiac MRI or radionuclide myocardial perfusion imaging confirmed myocardial ischemia and ECG ST-T changes in patients with CHD;
(2) Stable condition after surgical treatment with PCI;
(3) Aged no less than 18 years, and be not more than 70 years, regardless of gender;
(4) limb joint activity is normal, can complete Tai Chi exercise;
(5) Patients voluntarily participate in the trial and sign informed consent.
(1) Patients with severe cardiopulmonary diseases such as dissection of aortic, severe aortic coarctation, aortic aneurysm, pulmonary embolism, pulmonary infarction;
(2) Patients with severe cardiac arrhythmia;
(3) Patients with severe liver and kidney dysfunction and severe hematopoietic system abnormalities, water electrolyte abnormalities and other diseases;
(4) Patients with severe mental illness who have difficulty cooperating;
(5) Pregnant or lactating women;
(6) Patients with uncontrolled infectious or non-infectious inflammatory diseases;
(7) Patients who cannot perform this exercise after professional evaluation;
(8) Subjects who are participating in clinical trials of other drugs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Seattle Angina Questionnaire 24 weeks Five dimensions: the degree of restriction of physical activity, angina pectoris stable state, frequency of angina pectoris attack, satisfaction with treatment, and awareness of the disease.
- Secondary Outcome Measures
Name Time Method Cardiac function indicators 24 weeks left ventricular ejection fraction (LVEF) was measured by color doppler ultrasonic diagnostic apparatus