ACTRN12623001238662招募中Unknown
Feasibility and preliminary efficacy of a Hospital Fall Prevention Moments of Care intervention: a pilot trial
St John of God Midland Public and Private Hospital0 个研究点目标入组 10,000 人开始时间: 2023年11月30日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
- 入组人数
- 10,000
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
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •There are two ‘levels’ of participation:
- •1.Approximately 200 study ward caregivers responsible for providing patient care on study wards who will receive training to deliver the interventions prior to commencement. Eligible caregivers are nursing and allied health staff employed by SJGMPPH on study wards who engage with patients during moments of care when the intervention will be delivered. There are approximately 50 caregivers who work on each of the four study wards, rather than moving across different wards, including with permanent or casual SJGMPPH employment contracts. A purposive sample of these study ward caregivers will undertake a qualitative survey during follow-up to gather primary feasibility outcomes, and this will occur following written informed consent.
- •2.Patients who are admitted to study wards and may include people who are highly dependent on medical care or people with a cognitive impairment, an intellectual disability, or a mental illness. Patient state of alertness and cognition will be measured using the 4AT score (Anand et al., 2019), which is a validated cognitive screen already in use at the hospital as a part of usual care. Participants who are assessed as having possible cognitive impairment (4AT score between 1 and 3), or possible delirium and cognitive impairment (score of 4 or more), will continue to be included, and caregiver training will guide intervention delivery. A purposive sample of these patients will undertake a semi-structured survey during control and intervention delivery to determine feasibility outcomes, and this will occur following written informed consent.
排除标准
- •No exclusion criteria.
研究者
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