Implantable Cardioverter Defibrillator Recipients
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients who implant implantable heart devices with new defibrillation function 2.age>=20yo 3.Outpatient of the facility 4.informed consent can be obtained
Exclusion criteria
Exclusion criteria: 1.difficult walking independently 2.difficult to answer 3.patients not suitable for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To show the efficacy of the nursing supprt and self-management support by the trained nurses for the patients' better self-adjustment to the cardiac defibrillators | — |
Secondary
| Measure | Time frame |
|---|---|
| To show the efficacy of the nursing supprt and self-management support by the trained nurses for the better POMS2 score, QOL score,"Activity" and "Sleep" 6 months after discharge | — |
Countries
Japan
Contacts
Kobe University Graduate School of Medicine Section of Arrhythmia, Division of Cardiovascular Medicine, Department of Internal Medicine