Implantable Cardioverter Defibrillator Recipients
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Ptients with shock device treated with remortmonitaring system 2. age>=20yo 3. informed consent can be obtained
Exclusion criteria
Exclusion criteria: 1. patients not agree to particitating this study 2. patients not suitable for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To show the efficacy of the telephone interventions by the trained nurses for the patients' better self-adjustment to the cardiac defibrillators | — |
Secondary
| Measure | Time frame |
|---|---|
| To show the efficacy of the telephone interventions by the trained nurses for the patients' better QOL and anxiety score, and the rate of accidental admissions are also evaluated | — |
Countries
Japan
Contacts
Kobe University Graduate School of Medicine Section of Arrhythmia, Division of Cardiovascular Medicine, Department of Internal Medicine