ACTRN12626000941369进行中(未招募)不适用
The RECOVER Trial: Evaluating the Effectiveness and Implementation of Restoring Energy and Capacity in Older adults via aged care Embedded Rehabilitation
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 300
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 Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 65 Years 至 No limit(—)
- 性别
- All
入选标准
- •Older person receiving aged care services through partner organisations (residential or home-based care through Support at Home or Commonwealth Home Support).
- •Frail, determined using the Clinical Frailty Scale with a score of 5-
- •Recent history of viral illness (long COVID, Respiratory Syncytial Virus (RSV), influenza, gastroenteritis) identified through self-report, test, or clinical assessment. The World Health Organization’s COVID-19 case definitions of ‘suspected’, ‘probable’, or ‘confirmed’ infection will be used. Where applicable, testing would be via an antigen test which tests for COVID-19, RSV, and Influenza A&B (e.g., Covid-19/RSV/Influenza A&B Antigen Test).
- •Persistent symptoms (physical or cognitive fatigue) and/or functional decline (has not recovered to usual level of independence in daily activities) at 4 weeks (and up to 12 weeks) post-illness onset identified through care provider records or older person self-report.
- •Participants must have sufficient cognitive ability to be able to participate in the intervention (e.g. understand and follow simple instructions). This will be determined with a score of <10 using the PAS Subject Interview.
排除标准
- •Score of >10 using the PAS Subject interview tool.
- •Disruptive behaviours untenable for supervised exercise (e.g., agitation which causes distress to self or others) as documented in care provider data.
研究者
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