The Nurse-Peer-Led Support Intervention and Quality of Life in Patients with an Implantable Cardioverter Defibrillator
Not Applicable
- Conditions
- patients with an implantable cardioverter defibrillator.Presence of electronic cardiac devices
- Registration Number
- IRCT20180808040742N1
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
All patients with an Implantable Cardioverter Defibrillator
At least 3 months have passed since the insertion of Implantable Cardioverter Defibrillator.
Exclusion Criteria
Unwillingness to continue to participate in this study by the patient
The absence of more than two sessions of classes formed by nurses and peer
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of Life Score in the McNew Questionnaire. Timepoint: Before the intervention and 15 days after the intervention. Method of measurement: MacNew quality of life questionnaire.
- Secondary Outcome Measures
Name Time Method