Patient with Coronary Artery Bypass Grafting Surgery. 121-Acute myocardial infarction 122-Subsequent myocardial infarction 123-Certain current complications following acute myocardial infarction 125-Chronic ischaemic heart disease
Conditions
Interventions
Intervention 1: Second group will receive rehabilitation at home, take exercise program after being discharged from hospital, advised to exercise orderly and call doctor when having a problem. In orde
Rehabilitation
Second group will receive rehabilitation at home, take exercise program after being discharged from hospital, advised to exercise orderly and call doctor when having a problem. In order to motivate th
The study included two intervention groups and one control group. The first intervention group received hospital-based usual rehabilitation program from rehabilitation center of Tehran Heart Center
The control group with the same schedule as group 2 will be followed up by phone. For Ethical principles, we will advise control group to received rehabilitation program from rehabilitation center of
Sponsors
Vice Chancellor of research,Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
35 Years to 80 Years
Inclusion criteria
Inclusion criteria: “Inclusion criteria”: • stroke volume more than 40% • Coronary artery bypasses surgery recently in previous 4 to 8 weeks • Having a normal response to exercise test “Exclusion criteria”: • ventricular arrhythmias • atrial fibrillation • uncontrolled hypertension • type 2 diabetes • systemic disease and pulmonary that limited Sports • physical disabilities and any conditions limited Sports • severe valvular heart disease • known or suspected aortic dissection
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Score in Six minute walk test (MWT). Timepoint: 8 weeks after starting intervention. Method of measurement: Pedometr.;Rate Pressure Product. Timepoint: 12 Weeks after starting intervention. Method of measurement: Exercise Test.;Ejecton Fraction (EF). Timepoint: Based and 12 weeks later. Method of measurement: Echocardiography. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality Of Life. Timepoint: Base and 12 weeks later. Method of measurement: Questionnaire.;Tei index. Timepoint: 12 weeks after intervention. Method of measurement: Echocardiography.;Depression. Timepoint: Base and 12 weeks later. Method of measurement: Questionnaire.;Systolic and Diastolic Blood Pressure. Timepoint: At base and 12 weeks after intervention. Method of measurement: Sphygmanimeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNegar Omidi
Tehran Heart Center
Outcome results
None listed