A multicenter prospective cohort study utilizing ICF in elderly patients with heart failure
Not Applicable
- Conditions
- Symptomatic heart failure
- Registration Number
- JPRN-UMIN000045315
- Lead Sponsor
- Hiroshima University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
Those who were unable to give consent for this study Those who are judged by the physician in charge to be incapable of consenting to the study due to impaired consciousness, significant cognitive decline, or higher brain dysfunction. Those judged by the physician in charge to be incapable of consenting to the study due to consciousness disorder, significant cognitive decline, or higher brain dysfunction Those who are judged by the physician in charge to be inappropriate.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of life at 3 months and 1 year after discharge
- Secondary Outcome Measures
Name Time Method Medical and nursing care costs Re-admission nursing care level