Self-
Conditions
Interventions
In the test group,
volunteers with a history of coronary artery disease will be taught to other patients with coronary artery disease as a peer group. Training is carried out through a peer group for three consecutive h
hour sessions in groups with 4 to 5 participants. The intervals between sessions are one day. The content of the training includes prescription drugs,
diets (foods tailored to the condition of the disease),
and patient activities (how to do daily activities).,The control group receives routine care and training. In this way,
patients with coronary artery disease at the time of referral to the hospital will be given a brief explanation about how to use drugs,
lifestyle and daily activities for 10 minutes by nurses.
Experimental Behavioral,Active Comparator Behavioral
Peer Education Group,Control Routine Group
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
60 Years to 85 Years
Inclusion criteria
Inclusion criteria: Age 60 to 85 years old The absence of known psychological illness and the lack of use of psychiatric drugs, according to the patient Suffering from coronary artery disease Not having any cognitive, speech, or hearing disorder Not having pain during training The desire and ability to take care of yourself and adherence to treatment Having complete satisfaction to participate in the study, along with informed consent form
Exclusion criteria
Exclusion criteria: If any of the samples are exposed to critical conditions during the study, Critical conditions include chest pain, physical problems such as headache, dizziness, nausea, vomiting, hemodynamic problems, such as any changes in blood pressure Mental problems and any other conditions that lead to non-cooperation Patients who do not have the desire and willingness to participate in the study during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Self-care Before intervention and 7 day after intervention 34 items self-care assessment questionnaire,Quality of life Before intervention and 7 day after intervention 12-items quality of life questionnaire | — |
Secondary
| Measure | Time frame |
|---|---|
| Adherence to treatment Before intervention and 7 day after intervention 40-items adherence to treatment questionnaire | — |
Countries
Iran
Contacts
Public ContactMojtaba Roshandel
Shiraz University of Medical Sciences
Outcome results
None listed