Condition 1: Acute coronary syndrome (ACS). Condition 2: Self-management. Acute ischemic heart disease, unspecified
Conditions
Interventions
Intervention 1: Intervention group: The intervention is an educational intervention that has been prepared using reliable and up-to-date sources and has been approved by experts. Before the interventi
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All conscious patients, referred to this hospital, in whom the clinical and paraclinical diagnosis of ACS has been confirmed and are now ready to be discharged No participating in other studies or training sessions similar to this research during the last 6 months Having a smart phone and the ability to work with it
Exclusion criteria
Exclusion criteria: Lack of minimum reading and writing literacy Inability to salf-care (dependence on others) for any reason except ACS based on Barthel's ADL tool (completely dependent (0-8 points), relative dependence (9-12 points), Complete independence (13-20 points)} is determined. History of psychological disorder (use of antipsychotic drugs) which is determined based on the self-report of the patient or the patient's companion Cardiovascular disease as a complication of another chronic disease Congenital heart disease Inability to answer questions due to the disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Attitude. Timepoint: At the beginning of the study (before the start of intervention) and 2 months after intervention. Method of measurement: A researcher-made questionnaire which reliability and validity have been confirmed.;Perceived norm. Timepoint: At the beginning of the study (before the start of intervention) and 2 months after intervention. Method of measurement: A researcher-made questionnaire which reliability and validity have been confirmed.;Perceived behavioral control. Timepoint: At the beginning of the study (before the start of intervention) and 2 months after intervention. Method of measurement: A researcher-made questionnaire which reliability and validity have been confirmed.;Behavioral intention. Timepoint: At the beginning of the study (before the start of intervention) and 2 months after intervention. Method of measurement: A researcher-made questionnaire which reliability and validity have been confirmed. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Skineh Sabzevari
Kerman University of Medical Sciences
Outcome results
None listed