ACTRN12624000267550尚未招募Unknown
Effect of a Digital Peer Support Intervention for ICU Survivors on Health-Related Quality of Life: icuRESOLVE (icu Recovery Solutions Co-Designed through SurVivor Engagement) Randomised Controlled Trial
Department of Critical Care, The University of Melbourne0 个研究点目标入组 212 人开始时间: 2024年3月15日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 212
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
- •ICU admission >48 hours at participating hospital
- •Age 18 years and over
- •Access to digital platform (functioning computer, internet access and speed, capacity to log onto a video-sharing platform)
排除标准
- •Death anticipated as likely prior to day 90/180 outcome assessment
- •Deemed high risk of loss to follow up by research staff.
- •Diagnosed pre-existing or new cognitive conditions that would prevent ability to participate in the intervention or outcome assessment.
- •Referred or transferred to the Psychiatric Services during the hospitalisation period as identified in medical file
- •Severe neurological conditions (e.g. severe traumatic brain injury) that would prevent ability to participate in the intervention or outcome assessment.
- •Not expected to return home following discharge
- •Lack of either a reliable smartphone with a data plan or internet or a computer with internet, webcam and microphone access; or phone access
- •Unable to effectively communicate in English, and that would prevent ability to participate in the intervention or outcome assessment
- •Any other reason preventing participants from participating in intervention, including but not limited to: known criminal activity, known personality disorder.
研究者
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