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patient-reported outcomes (PROs) for palliative care patients receiving home-based care.

An intervention of Patient-Reported Outcomes (PROs) for cancer and non-cancer patients receiving home palliative care. - PROs

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1030260116
Enrollment
40
Registered
2026-05-08
Start date
2026-05-08
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

Patients needed for palliative care palliative care

Interventions

For patients receiving palliative care at home, we will administer the IPOS (Integrated Palliative Outcome Scale), a patient-reported outcome (PRO) assessment tool, every week to discuss the medical t
IPOS, QOL, home care, palliative care

Sponsors

Ishii Yoko
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients diagnosed with cancer, chronic heart failure, chronic kidney failure, chronic obstructive pulmonary disease, a rare neurological disorder, chronic liver failure, or cerebrovascular disease, as well as frail elderly patients who require palliative care Patients are identified through the use of a surprise question for screening patients requiring palliative care, where the healthcare provider determines that it would not be surprising if the patient died within one year. Adult (male or female) patients receiving home care who require palliative care and have provided informed consent for the study. Patients capable of communicating effectively. Participants must meet all of the above criteria.

Exclusion criteria

Exclusion criteria: Patients experiencing severe physical or mental distress, to the extent that healthcare professionals determine it is difficult for them to participate in the study Patients with significantly impaired cognitive function, making communication difficult Participants must fall into one of the above categories.

Design outcomes

Primary

MeasureTime frame
EORTC-QLQ-C15PAL

Secondary

MeasureTime frame
IPOS 3-Day Version for Patients FHU (Feeling Hard and Understood Conference participation rate

Contacts

Public ContactYoko Ishii

International University of Health and Welfare

ishii-yoko-og@ihwg.jp+81-8010155452

Outcome results

None listed

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