ISRCTN43049287已完成不适用
A comparison of training packages for deployment of mechanical chest compression devices in clinical practice: a randomised controlled manikin trial (COMPRESS-SIM)
niversity of Warwick0 个研究点目标入组 60 人开始时间: 2016年6月30日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
研究概览
简要总结
2018 results in https://www.ncbi.nlm.nih.gov/pubmed/29391379
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. NHS clinical staff (e.g. doctors, nurses, paramedics) that have current registration with a professional body (General Medical Council; Nursing and Midwifery Council; Health and Care Professions Council
- •2. Hold a current Resuscitation Council (UK) Immediate Life Support or Advanced Life Support qualification, or other equivalent resuscitation qualification
- •3. Provide written informed consent for participation
- •4. Prior to randomisation, participants must also have completed the manufacturer on-line training package on use of the device
排除标准
- •1. Staff that have an injury or disability that prevents the use or handling of the mechanical chest compression device
- •2. Receipt of formal training in use of the LUCAS-2 mechanical chest compression device in the last six months
研究者
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