The patient with an Implantable Cardioverter Defibrillator.
Conditions
Interventions
Intervention 1: Control group:This patients do not receive any intervention from the researcher and are discharged after receiving regular care at the facility. Intervention 2: Intervention group: The
Sponsors
Shaheed Rajaie's Cardiovascular Medical and Research Center
Eligibility
Sex/Gender
All
Age
20 Years to 80 Years
Inclusion criteria
Inclusion criteria: Being 20 to 80 years old Being ability to read, write, and speak in Persian Accessing phone call Implanting Cardioverter Defibrillator for the first time
Exclusion criteria
Exclusion criteria: Suffering from Cognitive Disorders Suffering from Commorbidity results in hospitalization Participation in other intervention program
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Self-efficacy. Timepoint: Before the intervention, immediately after ending the intervention. Method of measurement: Self-efficacy questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety. Timepoint: Before the intervention, immediately after ending the intervention. Method of measurement: Speil-berger State-Trait Anxiety Inventory.;Number of received shocks. Timepoint: Immediately after ending the intervention. Method of measurement: patient report.;Referrals outside of the plan to Medical centers. Timepoint: Immediately after ending the intervention. Method of measurement: patient report. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZakerimoghadam Masoumeh
Tehran University of Medical Sciences
Outcome results
None listed