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A multicenter prospective cohort study utilizing ICF in elderly patients with heart failure

A multicenter prospective cohort study utilizing ICF in elderly patients with heart failure - A multicenter cohort ICF study in elderly with heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000045315
Enrollment
200
Registered
2021-09-06
Start date
2021-10-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Symptomatic heart failure

Interventions

None listed

Sponsors

Hiroshima University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet the following eligibility criteria and do not meet the exclusion criteria will be eligible for the study among patients with insufficiency aged 75 years or older who are hospitalized at Hiroshima University Hospital and the collaborating research institutions. Eligibility criteria Patients admitted to the Department of Cardiology and the Department of Cardiovascular Surgery at the participating institutions with a diagnosis of symptomatic heart failure as the primary or secondary disease. Those who can provide written consent. Symptomatic heart failure refers to patients who meet the Framingham heart failure diagnostic criteria or who are judged by the attending physician to have symptoms of low cardiac output syndrome. Framingham heart failure diagnostic criteria.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Quality of life at 3 months and 1 year after discharge

Secondary

MeasureTime frame
Medical and nursing care costs Re-admission nursing care level

Countries

Japan

Contacts

Public ContactShigehito Shiota

Hiroshima University Hospital Department of Rehabilitation, Division of Clinical support

sshiota@hiroshima-u.ac.jp0822575566

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026