ISRCTN15863801已完成未知
Improving end of life care: supporting the workforce and reducing hospitalisations through an implementation study in care homes
niversity of Stirling0 个研究点目标入组 349 人开始时间: 2020年12月17日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 349
研究概览
简要总结
2021 Protocol article in https://pubmed.ncbi.nlm.nih.gov/33619205/ protocol (added 24/02/2021) 2024 Results article in https://pubmed.ncbi.nlm.nih.gov/39046763/ (added 25/07/2024)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Stakeholders (for interviews in Phase 1 & 2):
- •1. Work for specialist palliative care or a care home in one of the six cases; or are a resident in one of the care homes; or are a relative of a care home resident in one of the six cases; or work in acute care impacted by hospitalised care home residents
- •2. Willing to provide informed consent
- •3. Have capacity to provide their own consent to participate
- •4. Not engaged in any current safeguarding investigations
- •Care homes:
- •1. Located near to the specialist palliative care team
- •2. Provide care to residents who have high clinical nursing/medical needs
- •3. Willing to sign a memorandum of understanding with the research team, outlining provision of hospitalisation data, facilitate access to staff for interviews, and engagement in Needs Rounds
- •4. A range of sizes (focusing primarily on larger care homes, following CQC data indicating lower quality in larger facilities), sole traders and large corporate provider, and with a range of funding models (NHS/social care and self-funded residents)
- •1. Resident in a collaborating care home in one of the six case study locations
- •2. An anticipated life-expectancy <6 months, or a deteriorating condition where they are at risk from dying without an adequate care plan in place
- •3. Experiencing sub-optimal bio-psycho-social symptoms
- •Relatives completing 'family perceptions of care' questionnaire
- •1. Relative of a resident who was discussed in Needs Rounds
- •2. Able to provide their own informed consent
- •Interviewees (PPI evaluation)
- •1. Co-investigator or staff at one of the case study sites
- •2. Able to provide their own informed consent
排除标准
- •Does not meet inclusion criteria
研究者
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