myocardial infarction. Myocardial infarction (acute) NOS
Conditions
Interventions
Intervention 1: Control group: therapeutic touch at any false point in the stretch for two minutes and a total of 10 minutes and record physiological parameters before and after. Intervention 2: Group
Treatment - Drugs
Control group: therapeutic touch at any false point in the stretch for two minutes and a total of 10 minutes and record physiological parameters before and after
Groups: performing acupressure on five points at any point two minutes for 3 days in the morning and evening and record physiological parameters before and after the intervention of accupressure
Sponsors
Vice Chancellor for Research, Isfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
75 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria included: willingness to participate in the study; age 35 to 75 years; Myocardial Infarction; Alert; no particular problem in the practices of acupressure; stability in hemodynamical records Permission for Acupressure by acupressure specialist and cardiologist; excluding criteria: the patient's unwillingness to continue to participate in the intervention; the patient died during the study; doctor's intervention for excluding from study; the emergence of any circumstances at the time of intervention.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sistolic BP. Timepoint: 10 minutes before and Immediately after the intervention and 30 minutes after intervention. Method of measurement: Mercury sphygmomanometer in mmHg.;Diastol BP. Timepoint: 10 minutes before and Immediately after the intervention and 30 minutes after intervention. Method of measurement: Mercury sphygmomanometer in mmHg.;Heart rate. Timepoint: 10 minutes before and Immediately after the intervention and 30 minutes after intervention. Method of measurement: Finger Pulse Oximeter in terms of number of minutes.;O2 sat. Timepoint: 10 minutes before and Immediately after the intervention and 30 minutes after intervention. Method of measurement: Finger Pulse Oximeter in percent. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMarzieh Batvani
Isfahan University of Medical Sciences
Outcome results
None listed