The Physiologic and Emotional Effects of Augmented Reality Simulation Versus In Person Simulation - A Noninferiority, Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 111
- 试验地点
- 1
- 主要终点
- Parasympathetic response indexed by RSA
研究概览
简要总结
This study will evaluate the physiologic and emotional effects of an augmented reality (AR) simulation versus an in-person simulation. This is a single institution, non-inferiority, randomized controlled trial. The target enrollment will be 100 participants in each group for a total of 200 participants. One group will wear an AR headset and participate in an AR medical crisis scenario and the other group will participate in the same scenario with a traditional, mannequin based in situ simulation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Hospital providers, including nurses, physician assistants, physicians, physician trainees, and other healthcare workers at Lucile Packard Children's Hospital (LPCH) and affiliated facilities who communicate with patients daily will be included
排除标准
- •Participants with reported severe motion sickness
- •Seizure disorder
- •Currently using chronotropic heart medications, such as β blockers
研究组 & 干预措施
Augmented Reality Enhanced Simulation (Treatment group)
Participants will experience augmented simulations with a holographic mixed-reality setting based on different workplace scenarios such as medical error and workplace harassment via Augmented Reality (AR) headset.
干预措施: Augmented Reality Headset (Behavioral)
Traditional In Situ Simulation (Control group)
Participants will experience in-person simulations of different workplace scenarios such as medical error and workplace harassment
结局指标
主要结局
Parasympathetic response indexed by RSA
时间窗: Duration of simulation (15-20 minutes)
Measured via respiratory sinus arrhythmia (RSA) in hertz using chest biometric sensors in 30-second epochs.
次要结局
- ISO 9241-400(Post-simulation (5 minutes))
- Sytem Usability Scale (SUS)(Post-simulation (5 minutes))
- Simulation Design Scale (SDS)(Post-simulation (5-10 minutes))
- Learning effectiveness(5 months-post simulation (5 minutes))
研究者
Thomas Caruso
Clinical Associate Professor
Stanford University