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A Study of the Effectiveness of Hospice Informational Tool Interventions in Home Care for Patients with Advanced Cancer

A Study of the Effectiveness of Hospice Informational Tool Interventions in Home Care for Patients with Advanced Cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077346
Enrollment
Unknown
Registered
2023-11-06
Start date
2023-11-07
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

terminal stage of cancer

Interventions

intervention group:Patients receive routine patient care + home hospice informational tools (content includes analysis of common symptoms of advanced cancer, home care tips, symptom observation scales
control subjects:Patients receive routine patient care while at home.

Sponsors

Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Clear clinical diagnosis:Patients with a clear clinical diagnosis of receiving palliative care and a KPS = 70 on the Kahn Functional Rating Scale. Patient Awareness, Recognition, Willingness and Informed Consent:Ensure that the patient has sufficient cognition, understanding and verbal communication skills to understand the purpose, process and ethos of the study and voluntarily participates in the study. It may be necessary to obtain informed consent from patients with sufficient cognition, understanding and verbal communication skills to voluntarily participate in the study Family support and care: Consider whether the patient has stable family support and an appropriate home care environment to ensure that they are able to fully utilize and benefit from the tools. Availability of stable family support and home care setting Technology accessibility and adaptability:Assess whether the patient has the technological capacity to use the informatics tool and determine whether they are able to adapt and use the tool. Have a cell phone or tablet, registered for a WeChat account, and be able to operate and browse regular web content.

Exclusion criteria

Exclusion criteria: Comorbid mood, psychological dysfunction such as severe depression and anxiety, severe cognitive impairment, severe mental illness Incomplete clinical information or withdrawal Comorbidities of other chronic diseases, acute infectious diseases such as AIDS, etc. Living alone, without home caregiver or family support

Design outcomes

Primary

MeasureTime frame
Assessment of anxiety;Assessment of depression;Quality of life assessment;

Secondary

MeasureTime frame
Patient family satisfaction ratings;

Countries

China

Contacts

Public ContactLiang Ji

Fudan University

jliang@shmu.edu.cn+86 136 2169 3588

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026