Acute Coronary Syndrome. Acute ischemic heart disease, unspecified
Conditions
Interventions
Intervention 1: Intervention group: On the first day, for patients with acute coronary syndrome in the hospital, once their physical and mental conditions stabilize, education is provided by the inter
Sponsors
Khomein School of Medical Sciences
Eligibility
Sex/Gender
All
Age
30 Years to No maximum
Inclusion criteria
Inclusion criteria: Diagnosis of acute coronary syndrome by a cardiologist Age = 30 of the participants BMI 90%
Exclusion criteria
Exclusion criteria: No diagnosis of heart failure in the study subject No history of specific diseases: individuals with a history of respiratory diseases such as asthma, COPD, bronchitis, etc., or heart surgery within the past two months. Absence of cardiac dysrhythmia in the study subject No history of mental illness, because psychological problems can affect the patient's ability to participate in the intervention. No cognitive impairments affecting the ability to learn and perform breathing techniques No history of myocardial infarction in the past two weeks No use of any other breathing or relaxation techniques in the intervention and control groups to prevent cross-effects of other interventions. Non-smoking No diagnosis of rheumatoid arthritis Participants who develop serious complications, such as uncontrolled cardiac disorders, requiring exclusion from the study to prevent harm to them. Participants' unwillingness to continue the study for any reason Feeling discomfort while performing the Buteyko breathing technique
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pittsburgh Sleep Quality Index Score. Timepoint: At the beginning of the study, 7, 14, 21, 28, 35, 42. Method of measurement: Pittsburgh Sleep Quality Index.;Fatigue Score of the Multidimensional Fatigue Inventory. Timepoint: At the beginning of the study, 7, 14, 21, 28, 35, 42. Method of measurement: Multidimensional Fatigue Inventory.;Peripheral Oxygen Saturation. Timepoint: 1 day after the first implementation of the intervention. Method of measurement: Pulse Oximeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMarziyeh Mousivand
Khomein School of Medical Sciences
Outcome results
None listed