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Clinical Trials/ACTRN12623000576628
ACTRN12623000576628
Completed
未知

Feasibility of routine collection of patient reported outcome measures (PROMs) using a co-designed collection system in general medicine and rehabilitation ward patients

Peninsula Health0 sites131 target enrollmentMay 25, 2023

Overview

Phase
未知
Intervention
Not specified
Conditions
Rehabilitation
Sponsor
Peninsula Health
Enrollment
131
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 25, 2023
End Date
March 1, 2024
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Consumer Participants:
  • Consumer participants will include all patients aged 60 years or older on the participating acute general medicine and sub\-acute inpatient general rehabilitation wards at Peninsula Health who are discharged to a private residence or residential aged care home during the study period. Patients with cognitive or communication impairments will complete the PROM via proxy (i.e., family member, next of kin, carer completes the PROM on their behalf) as per recommendations for use of the EQ\-5D\-5L. Therefore, participants will consist of two groups:
  • 1\)Patients aged 60 years or older with cognitive capacity to complete the PROM
  • 2\)Carers/Next of Kin of patients who are 60 years or older without capacity to complete the PROM
  • Volunteer Participants:
  • Volunteer participants will include all Peninsula Health volunteers who volunteer their time to assisting with the administration of PROMs on the participating wards during the trial.

Exclusion Criteria

  • Consumer Participants:
  • 1\) Not meeting the inclusion criteria
  • 2\) Death\- no further PROMs or surveys will be administered
  • 3\) No cognitive or communicative capacity to participate and no Carer/NOK available to participate on their behalf
  • Volunteer Participants:
  • \- Volunteers not affiliated with Peninsula Health will not be eligible for inclusion.

Outcomes

Primary Outcomes

Not specified

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