Condition 1: Acute Coronary Syndrome. Condition 2: Acute Coronary Syndrome. Condition 3: Acute Coronary Syndrome. Condition 4: Acute Coronary Syndrome. Condition 5: Acute Coronary Syndrome. Condition 6: Acute Coronary Syndrome. Condition 7: Acute Coronary Syndrome. Unstable angina Acute transmural myocardial infarction of anterior wall Acute transmural myocardial infarction of inferior wall Acute transmural myocardial infarction of other sites Acute transmural myocardial infarction of unspe
Conditions
Interventions
Intervention 1: The intervention group will do the rhythmic breathing for twenty minutes every five minutes once and it will take a minute and during their breathing will focus only on entering and le
In control group, the intervention will not take place except routine treatments.
The intervention group will do the rhythmic breathing for twenty minutes every five minutes once and it will take a minute and during their breathing will focus only on entering and leaving air. In th
Sponsors
Investigator
Eligibility
Sex/Gender
All
Age
8 Years to 92 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Volunteer for research; ACS definitive diagnosis by the cardiologist; Lack of critical state of health (no cardiac dysrhythmia, hemodynamic and peripheral capillary oxygen saturation less than 80%) licensed clinician; Non-smoking; Lack of alcoholism and drug; Lack of respiratory diseases, gastrointestinal, diabetes and mental recognized and diagnosed by a physician; Age between 15-85 years Exclusion criteria: Lack of satisfaction for cooperation; Create a life-threatening situation; The creation of any intervening circumstances that made it impossible to continue
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Chest pain. Timepoint: Before and during 12 hours after intervention. Method of measurement: McGill pain scale.;Systolic and diastolic blood pressure. Timepoint: Before and during 12 hours after intervention. Method of measurement: Monitoring.;Respiratory rate. Timepoint: Before and during 12 hours after intervention. Method of measurement: Monitoring.;Respiratory rythme. Timepoint: Before and during 12 hours after intervention. Method of measurement: Monitoring.;Pulse rate. Timepoint: Before and during 12 hours after intervention. Method of measurement: Monitoring.;Pulse rythme. Timepoint: Before and during 12 hours after intervention. Method of measurement: Electrocardiogram.;Peripheral capillary oxygen saturation. Timepoint: Before and during 12 hours after intervention. Method of measurement: Pulse oxymeter.;The need for drug. Timepoint: Before and during 12 hours after intervention. Method of measurement: Patient pan card. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNarges Saber
Gonabad University of Medical Sciences
Outcome results
None listed