Feasibility of routine collection of patient reported outcome measures
- Conditions
- RehabilitationHealth Services ResearchPhysical Medicine / Rehabilitation - Other physical medicine / rehabilitationGeneral medicineGeriatric MedicinePublic Health - Health service research
- Registration Number
- ACTRN12623000576628
- Lead Sponsor
- Peninsula Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 131
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
And
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.
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method