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临床试验/NCT03863314
NCT03863314已完成不适用

Virtual Reality vs Inperson Simulation: A Non-inferiority Study

Stanford University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2019年7月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
120
试验地点
1
主要终点
Respiratory sinus arrhythmia

研究概览

简要总结

The purpose of this study is to determine if Virtual Reality (VR) can elicit emotional responses that are captured via physiological biometrics such as heart rate variability and skin conductance levels. As a non-inferiority study the investigators anticipate the technologies will elicit an emotional not inferior to those responses of an in-person simulations of workplace scenarios (i.e medical error and workplace harassment).

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

  • •Greater than 18 years of age
  • •Personnel working or volunteering at Lucile Packard Children's Hospital (LPCH) or Stanford Health Care (SHC) facilities

排除标准

  • •Patients who do not consent
  • •Are currently taking beta blockers or other chronotropic heart medication(s)
  • •Have a history of severe motion sickness
  • •Currently have nausea
  • •Currently experiencing seizures
  • •Are clinically unstable

研究组 & 干预措施

In-Person Simulation

Active Comparator

Participants will experience in-person simulations of different workplace scenarios such as medical error and workplace harassment

干预措施: In-person Simulation (Other)

Virtual Simulation

Experimental

Participants will experience virtual simulations of different workplace scenarios such as medical error and workplace harassment via Virtual Reality headset.

干预措施: Virtual Simulation (Device)

结局指标

主要结局

Respiratory sinus arrhythmia

时间窗: Throughout duration of simulation, approximately 15 minutes

Biometric sensors will be placed in strategic locations in order to collect respiratory sinus arrhythmia throughout either in-person or virtual simulation

次要结局

  • Emotional levels(Throughout duration of intervention, two minutes before and after the intervention)
  • Skin conductance levels(Throughout duration of simulation, approximately 15 minutes)
  • VR Simulation Questionnaire(Three months post study, approximately 5 minutes)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas Caruso

Clinical Associate Professor

Stanford University

研究点 (1)

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