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Trial registered on ANZCTR


Registration number
ACTRN12622000773730
Ethics application status
Approved
Date submitted
18/05/2022
Date registered
31/05/2022
Date last updated
4/07/2022
Date data sharing statement initially provided
31/05/2022
Type of registration
Retrospectively registered

Titles & IDs
Public title
Nurse led volunteer support interventions and a technology driven pain assessment
for older adults in hospital
Scientific title
Effectiveness of nurse led volunteer support interventions and a technology driven pain assessment for older adults in hospital
Secondary ID [1] 305104 0
None
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Extended hospital admission 323325 0
Pain 323326 0
Clinical incidents 326378 0
Condition category
Condition code
Physical Medicine / Rehabilitation 320888 320888 0 0
Other physical medicine / rehabilitation
Public Health 320889 320889 0 0
Health service research

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
All patients will have their pain assessed by nurses utilizing the PainChek® Universal and all patients will be offered one-to-one volunteer support across morning and afternoon shifts from Monday to Friday during their inpatient admission on the study wards at Joondalup Health Campus.
Volunteer support consists of assisting patients with activities related to orientation, cognition, sensory, mobility (encouraging and walking with ambulant patients; encouraging the patient to complete exercises), nutrition ( encouraging the patient to eat, and assisting with the set-up of meals), and wellbeing support (such as providing hand and foot massage, hair brushing) the nurse The duration of the volunteer support will be recorded on the volunteer Support Care plan.
For patients who are able to report their pain using the Numerical Rating Scale 0-10, nurses will assess the pain and record the outcome in PainChek® Universal application. For patients who are unable to report their pain using NRS the nurse will assess the patients pain using the PainChek application within PainChek Universal. Using AI, facial recognition and smartphone technology, PainChek® intelligently automates the pain assessment process at the point of care.
Intervention code [1] 323489 0
Treatment: Other
Comparator / control treatment
A historical control group comprising patients admitted to the same two wards at Joondalup Health Campus in the same period one year prior to the practice change (1 April 2021- 1 April 2022) will be used as the comparator group
Control group
Historical

Outcomes
Primary outcome [1] 331232 0
Length of stay obtained from hospital administrative data from hospital medical records
Timepoint [1] 331232 0
Discharge
Secondary outcome [1] 409260 0
Falls incidence obtained from hospital administrative data from hospital clinical incidence management system.
Timepoint [1] 409260 0
Data collected after final day during hospitalisation
Secondary outcome [2] 409261 0
Incidence of delirium obtained from hospital administrative data from hospital clinical incidence management system.
Timepoint [2] 409261 0
Data collected after final day during hospitalisation
Secondary outcome [3] 409262 0
Incidence of behavioural incidents obtained from hospital administrative data from hospital clinical incidence management system.
Timepoint [3] 409262 0
Data collected after final day during hospitalisation
Secondary outcome [4] 409263 0
Incidence of death obtained from hospital administrative data from hospital medical records
Timepoint [4] 409263 0
Data collected after final day during hospitalisation
Secondary outcome [5] 409264 0
Incidence of pressure injuries obtained from hospital administrative data from hospital clinical incidence management system.
Timepoint [5] 409264 0

Data collected after final day during hospitalisation
Secondary outcome [6] 409265 0
Incidence of analgesic use obtained from hospital pharmacy management system.
Timepoint [6] 409265 0


Data collected after final day during hospitalisation

Eligibility
Key inclusion criteria
Patients admitted to two geriatric medical wards at an acute metropolitan tertiary hospital in Perth, Western Australia.
Minimum age
65 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Nil

Study design
Purpose of the study
Prevention
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis
The study sample has been calculated based on the approximate number of patient admissions during the study period.
Descriptive statistics will be presented with means and standard deviations for parametric data, median and interquartile range for non-parametric data, and frequency for baseline characteristics. The clinical outcomes will be analysed using t-tests.

Recruitment
Recruitment status
Recruiting
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)
WA
Recruitment hospital [1] 22401 0
Joondalup Health Campus - Joondalup
Recruitment postcode(s) [1] 37566 0
6027 - Joondalup

Funding & Sponsors
Funding source category [1] 309498 0
Charities/Societies/Foundations
Name [1] 309498 0
Ramsay Hospital Research Foundation
Country [1] 309498 0
Australia
Primary sponsor type
University
Name
Edith Cowan University
Address
100 Joondalup Drive
Joondalup. WA. 6027.
Country
Australia
Secondary sponsor category [1] 310476 0
None
Name [1] 310476 0
Address [1] 310476 0
Country [1] 310476 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 309284 0
Ramsay Health Care WA/SA HREC
Ethics committee address [1] 309284 0
Ethics committee country [1] 309284 0
Australia
Date submitted for ethics approval [1] 309284 0
Approval date [1] 309284 0
25/10/2021
Ethics approval number [1] 309284 0
2134W
Ethics committee name [2] 310983 0
Edith Cowan University HREC
Ethics committee address [2] 310983 0
Ethics committee country [2] 310983 0
Australia
Date submitted for ethics approval [2] 310983 0
01/11/2021
Approval date [2] 310983 0
17/02/2022
Ethics approval number [2] 310983 0
2021-03014-SAUNDERS

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

Contacts
Principal investigator
Name 113622 0
A/Prof Rosemary Saunders
Address 113622 0
Edith Cowan University
100 Joondalup Drive
Joondalup WA 6027
Country 113622 0
Australia
Phone 113622 0
+61 08 63043513
Fax 113622 0
Email 113622 0
rosemary.saunders@ecu.edu.au
Contact person for public queries
Name 113623 0
Rosemary Saunders
Address 113623 0

Edith Cowan University
100 Joondalup Drive
Joondalup WA 6027
Country 113623 0
Australia
Phone 113623 0
+61 08 63043513
Fax 113623 0
Email 113623 0
rosemary.saunders@ecu.edu.au
Contact person for scientific queries
Name 113624 0
Rosemary Saunders
Address 113624 0

Edith Cowan University
100 Joondalup Drive
Joondalup WA 6027
Country 113624 0
Australia
Phone 113624 0
+61 08 63043513
Fax 113624 0
Email 113624 0
rosemary.saunders@ecu.edu.au

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


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.