ACTRN12623000576628已完成Unknown
Feasibility of routine collection of patient reported outcome measures (PROMs) using a co-designed collection system in general medicine and rehabilitation ward patients
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 131
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Diagnosis
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 60 Years 至 o limit(—)
- 性别
- All
入选标准
- •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.
排除标准
- •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.
研究者
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