Home medical care support study in patients with Left Ventricular Assist Devices using Social Networking Service.
Not Applicable
Recruiting
- Conditions
- Patients with Left Ventricular Assist Devices
- Registration Number
- JPRN-UMIN000030617
- Lead Sponsor
- Department of Cardiovascular Medicine, Saga University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Without access to a telephone line. (2) Patients who refused to participate in the study (3) Patients who are considered not eligible for the study by the attending doctor due to other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time in therapeutic range (TTR) from baseline to Last follow-up
- Secondary Outcome Measures
Name Time Method (1) Cumulative incidence of LVAD complications that associated with anticoagulation therapy and skin penetration management. (2) Number of cumulative incidences of other LVAD complications ( Devices trouble, Right heart failure, Aortic regurgitation, Arrhythmia, etc. ) (3) TTR ( 30 days before development of LVAD complications ) (4) All-cause death (5) Adherence (6) Number of cumulative onset of other adverse events (7) Hospital Anxiety and Depression Scale of patients and care givers