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Trial registered on ANZCTR


Registration number
ACTRN12625000891426
Ethics application status
Approved
Date submitted
18/06/2025
Date registered
15/08/2025
Date last updated
15/08/2025
Date data sharing statement initially provided
15/08/2025
Type of registration
Retrospectively registered

Titles & IDs
Public title
Quality Indicators of End-of-Life Care for Elderly Patients from Residential Aged Care Facilities
Scientific title
Quality Indicators of End-of-Life Care for Elderly Patients from Residential Aged Care Facilities
Secondary ID [1] 314695 0
Nil known
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Palliative Care 337878 0
Condition category
Condition code
Public Health 334208 334208 0 0
Health service research

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
Timeframe of retrospective data review: 1st July 2022 to 30th June 2024
Specialist community palliative care referral, which is a standard practice that residents at an aged care facility may access regardless of their involvement in this study. This involves at least one-on-one face-to-face consultation by a specialist palliative care clinical nurse consultant and/or specialist palliative medicine physician. During this review as part of standard routine clinical practice a patient-assessed and a physician-assessed score is recorded for symptom severity using the Palliative Care Problem Severity Score (PCPSS) and the Symptom Assessment Scale (SAS). Based on this assessment a decision may be made to prescribe medicines directed towards symptom management and comfort care and we will record if opioids, benzodiazepines, anti-emetics, antipsychotics or anti-secretory agents were prescribed to the patient. This retrospective data review will include review of the medicines recorded/prescribed by the community palliative care team for all patients admitted to the community palliative care service.
Intervention code [1] 331301 0
Not applicable
Comparator / control treatment
No control group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 341872 0
Primary palliative care diagnosis
Timepoint [1] 341872 0
Final palliative care team review prior to death.
Secondary outcome [1] 448848 0
Congruence of place of death with preferences
Timepoint [1] 448848 0
Final palliative care team review prior to death.
Secondary outcome [2] 448850 0
Prescription of end-of-life care medications (e.g. opioids, benzodiazepines, anti-emetics, anti-psychotics and anti0secretory agents)
Timepoint [2] 448850 0
Final palliative care team review prior to death.
Secondary outcome [3] 450498 0
Palliative Care Symptom Severity Score
Timepoint [3] 450498 0
The last palliative care team review of the patient prior to death
Secondary outcome [4] 450499 0
Symptom Assessment Scale
Timepoint [4] 450499 0
At the time of the last palliative care team review prior to patient death
Secondary outcome [5] 450812 0
Family meeting
Timepoint [5] 450812 0
Any of the palliative care team reviews prior to patient death
Secondary outcome [6] 450813 0
Medical treatment decision maker
Timepoint [6] 450813 0
Time of death.
Secondary outcome [7] 450814 0
Advanced Care Plan
Timepoint [7] 450814 0
Time of death

Eligibility
Key inclusion criteria
Age greater than or equal to 65 years
Residing in residential aged care facility
Death between 1st July 2022 and 30th June 2024 at a Cabrini Health site or who were admitted to the Cabrini Palliative Homecare service at their residential aged care facility at the time of death
Minimum age
65 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Death at a non-Cabrini health service our outside of the residential aged care facility

Study design
Purpose
Duration
Selection
Timing
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC

Funding & Sponsors
Funding source category [1] 319245 0
Hospital
Name [1] 319245 0
Cabrini Health
Country [1] 319245 0
Australia
Primary sponsor type
Hospital
Name
Cabrini Health
Address
Country
Australia
Secondary sponsor category [1] 321717 0
None
Name [1] 321717 0
Address [1] 321717 0
Country [1] 321717 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 317822 0
Alfred Hospital Ethics Committee
Ethics committee address [1] 317822 0
Ethics committee country [1] 317822 0
Australia
Date submitted for ethics approval [1] 317822 0
04/11/2024
Approval date [1] 317822 0
06/11/2024
Ethics approval number [1] 317822 0
Ethics committee name [2] 317824 0
Cabrini Research and Governance
Ethics committee address [2] 317824 0
Ethics committee country [2] 317824 0
Australia
Date submitted for ethics approval [2] 317824 0
05/12/2024
Approval date [2] 317824 0
09/12/2024
Ethics approval number [2] 317824 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 142270 0
Dr Merlina Sulistio
Address 142270 0
Cabrini Health, 181-183 Wattletree Road, Malvern VIC 3144
Country 142270 0
Australia
Phone 142270 0
+61 03 9508 1163
Fax 142270 0
Email 142270 0
Contact person for public queries
Name 142271 0
Elizabeth Brookes
Address 142271 0
Cabrini Health, 181-183 Wattletree Road, Malvern VIC 3144
Country 142271 0
Australia
Phone 142271 0
+61 03 9508 1163
Fax 142271 0
Email 142271 0
Contact person for scientific queries
Name 142272 0
Elizabeth Brookes
Address 142272 0
Cabrini Health, 181-183 Wattletree Road, Malvern VIC 3144
Country 142272 0
Australia
Phone 142272 0
+61 03 9508 1163
Fax 142272 0
Email 142272 0

Data sharing statement
Will the study consider sharing individual participant data?
No


What supporting documents are/will be available?

No Supporting Document Provided


Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.