Cardiac rehabilitation. Angina pectoris, unspecified
Conditions
Interventions
Intervention 1: Intervention group: In this group, cardiac rehabilitation will be conducted through 6 sessions at the center and another 6 sessions at home. Each cardiac rehabilitation exercise sessio
Sponsors
Isfahan Cardiovascular Research Institute
Eligibility
Sex/Gender
All
Age
30 Years to 80 Years
Inclusion criteria
Inclusion criteria: The patient has been treated for ischemic heart disease in one of the hospitals in Isfahan City At least two weeks have passed since PCI or 4 weeks since CABG The minimum age for participation in the study is 30 years, and the maximum age is 80 years
Exclusion criteria
Exclusion criteria: Contraindications for cardiac rehabilitation Patients who do not consent to participate in the study Physician's non-consent for patient's participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Average functional capacity (METs) of patients based on exercise test. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Exercise test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life score based on MacNew questionnaire. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: MacNew questionnaire.;Anxiety score in Spielberger questionnaire. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Spielberger questionnaire.;Depression score in Beck questionnaire. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Beck questionnaire.;The amount of physical activity based on the IPAQ questionnaire. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: IPAQ questionnaire.;Smoking. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Questionnaire.;Serum level of Triglyceride. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Testing the patient blood sample.;The changes in systolic blood pressure. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Sphygmomanometer.;The changes in body mass index (BMI). Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Body mass index formula.;Fasting blood sugar level. Timepoint: At the beginning of the study (prior to intervention) and at the end of the study after 12 rehabilitation sessions. Method of measurement: Testing the patient blood sample.;The changes in diastolic blood pressure. Timepoint: At the beginning of the study (prior t | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSina Rouhani
Esfahan University of Medical Sciences
Outcome results
None listed