Effect of combined yoga and rehabilitation in CABG patients
Not Applicable
- Conditions
- coronary artery bypass grafting.Atherosclerosis of coronary artery bypass graft(s) and coronary artery of transplanted heart with angina pectoris
- Registration Number
- IRCT20180728040615N1
- Lead Sponsor
- Shahid Rajaee Heart Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 30
Inclusion Criteria
Patients who underwent coronary artery bypass graft surgery in Shahid Rajai's Heart Hospital
45-75 years old.
At least one month have passed since surgery
Exclusion Criteria
Having a history of heart attacks, heart surgery or congestive heart failure
Major motor disturbances
Having more than 100 km distance from Shahid Rajaee Cardiac Rehabilitation Center in Tehran
Having ejection fraction at least 35%
Drug use and smoking
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Electerocardiographic changes. Timepoint: 48 hours before the intervention begins and 48 hours after the end of the training period. Method of measurement: It is measured by an electrocardiogram device in the Shahid Rajaie Cardiology and Cardiology Hospital.;Cardiac autonomic changes. Timepoint: 48 hours before the intervention begins and 48 hours after the end of the training period. Method of measurement: Measurement of heart rate variability with existing Holter device in Shahid Rajaee Heart Hospital, measurement of salivary alpha amylase and cortisol at rest.
- Secondary Outcome Measures
Name Time Method Heart rate variability( HRV). Timepoint: 48 hours before the training period and 48 hours after the training period. Method of measurement: Holter monitoring 24 hours.;Salivary Cortisol. Timepoint: 48 hours before and after of training period. Method of measurement: Take saliva in the form of fasting at rest in saliva special tubes.;Salivary amylase alpha. Timepoint: At the beginning of the study and 48 hours before the intervention, and 48 hours after the end of the intervention,. Method of measurement: Take saliva in the form of fasting at rest in saliva special tubes.