ISRCTN15676570进行中（未招募）未知
A multi-centre, single-arm feasibility study of a complex intervention to improve Recovery after an Episode of Delirium in adults over 65 years: the RecoverED study
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 入组人数
- 120
研究概览
简要总结
2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37715277/ (added 18/09/2023)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Current participant inclusion criteria as of 01/11/2023:
- •1. Aged over 65 years
- •2. Admitted to an acute hospital
- •3. Clinical diagnosis of delirium while admitted to hospital
- •4. Expected to be living in a private dwelling after discharge from hospital or immediate care (a period of 4 weeks of intermediate care will be allowed before discharge home)
- •5. Has a carer who could be approached for the study
- •6. Has the capacity to provide informed consent to participate, OR, has a consultee who is able to give an opinion on the participation of the person with delirium (in England), OR, has a relative/welfare guardian who is able to give informed consent on behalf of the person with delirium (in Scotland).
- •7. Lives within the geographical boundary of the local intervention delivery team
- •1. Family member or friend of the person with delirium
- •2. In contact with patient participant for at least one hour per week
- •3. Able to communicate in English sufficiently well to complete the proxy outcome measures
- •4. Has the capacity to provide informed consent.
- •Previous participant inclusion criteria:
- •1. Aged over 65 years
- •2. Admitted to an acute hospital
- •3. Clinical diagnosis of delirium lasting for more than 48 hours
- •4. Expected to be living in a private dwelling after discharge from hospital or immediate care (a period of 4 weeks of intermediate care will be allowed before discharge home)
- •5. Has a carer who is willing to assist with the completion of outcomes
- •6. Has the capacity to provide informed consent to participate, OR, has a consultee who is able to give an opinion on the participation of the person with delirium (in England), OR, has a relative/welfare guardian who is able to give informed consent on behalf of the person with delirium (in Scotland)
- •1. Family member or friend of the person with delirium who is going to take part in the study
- •2. In contact with patient participant for at least 1 hour per week
- •3. Able to communicate in English sufficiently well to complete the proxy outcome measures
- •4. Has the capacity to provide informed consent
排除标准
- •Current participant exclusion criteria as of 01/11/2023:
- •1. Diagnosis of delirium cannot be confirmed during the patient’s hospital visit
- •2. Unable to communicate verbally due to advanced dementia or aphasia
- •3. Carer declines participation in the study
- •4. Undergoing end-of-life care
- •5. Participating in another intervention study
- •There are no exclusion criteria for carer participants
- •Previous participant exclusion criteria:
- •1. Diagnosis of delirium cannot be confirmed during the patient’s hospital visit
- •2. Unable to communicate verbally due to advanced dementia or aphasia
- •3. Carer declines participation in the study
- •4. Undergoing end-of-life care
- •5. Participating in another intervention study
- •There are no exclusion criteria for carers
研究者
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