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Testing a new model of community based palliative care

A randomised controlled trial on effect of a multidisciplinary model of community palliative care on patient-centred care in preferred place

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12620001063909
Acronym
HPC3
Enrollment
500
Registered
2020-10-16
Start date
2020-11-01
Completion date
2021-11-01
Last updated
2020-10-26

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

Conditions

None listed

Brief summary

We will pilot a community palliative care coordination package in an urban and rural setting within Hunter New England Local Health District. We hypothesise that earlier identification of distress through routine surveillance in our community based patient together with the availability of a pool of Assistants in Nursing will improve the number of days spent in the place of preference (home).

Interventions

Community based palliative care patients randomised to the intervention arm will have their care managed by a care coordinator (clinical nurse specialist). Once stable they will receive weekly contact to identify any new symptoms or needs and they will be addressed as necessary. If required, patients can access assistant in nursing support in their home during unstable periods. The duration and frequency of the intervention will be based on needs identified. All interventions will be based in th

Community based palliative care patients randomised to the intervention arm will have their care managed by a care coordinator (clinical nurse specialist). Once stable they will receive weekly contact to identify any new symptoms or needs and they will be addressed as necessary. If required, patients can access assistant in nursing support in their home during unstable periods. The duration and frequency of the intervention will be based on needs identified. All interventions will be based in the patient's residence in person. The total duration of the study will be 12 months or until end of life.

Sponsors

Calvary Mater Newcastle
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

New referral to palliative care, based in the community and intending to receive their care at home and consent to participate in research

Exclusion criteria

None

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026