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临床试验/NCT07155681
NCT07155681尚未招募不适用

Evaluating Healthcare Professionals' Satisfaction and Stress Mitigation Using Virtual Reality Intervention in Surgical Ward: a Multination Feasibility Study

Amsterdam UMC, location VUmc2 个研究点 分布在 2 个国家目标入组 75 人开始时间: 2025年11月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
75
试验地点
2
主要终点
AIM-IAM-FIM • Acceptability of Intervention Measure (AIM), • Intervention Appropriateness Measure (IAM), • Feasibility of Intervention Measure (FIM)

研究概览

简要总结

The goal of this feasibility study is to learn whether a VR intervention is feasible, acceptable, and satisfactory for healthcare workers in surgical wards to help mitigate stress. Secondary objectives include assessing its potential contribution to stress reduction, user comfort, and practical integration into daily workflows.

Participants will take part in a single 10-minute VR intervention session.

详细描述

This study investigates the use of the HealthyMind Virtual Reality (VR) application as an innovative intervention to reduce stress among healthcare workers in surgical departments. Although workplace stress is common, there is currently a lack of structured interventions to address it.

The VR application provides healthcare professionals with the opportunity to relax through immersive, calming three-dimensional environments, such as a sunset by the sea or a mountain landscape. The VR headset is paired with an armband that non-invasively measures physiological parameters, including heart rate and heart rate variability. Based on these data, the VR environment automatically adapts to the user's stress level, for example by introducing a guided breathing exercise.

The intervention can be used at any self-selected moment during a shift, with the aim of offering a short and effective recovery break. The primary aim of this study is to evaluate the feasibility, acceptability, and user satisfaction of the VR intervention among healthcare workers. Secondary objectives include assessing its potential contribution to stress reduction, user comfort, and practical integration into daily workflows.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

入选标准

  • Volunteering healthcare professionals (≥18 years old) working in direct patient care, such as nurses, residents, physician assistants, and surgeons, on the surgical ward.

排除标准

  • Diagnosed with epilepsy
  • Experienced VR as a trigger for their migraines
  • Severe dizziness, nausea or physical disabilities will be excluded.
  • Diagnosed with arrythmias, bradycardia or tachycardia
  • Not able to wear the VR headset due to physical or psychological conditions

结局指标

主要结局

AIM-IAM-FIM • Acceptability of Intervention Measure (AIM), • Intervention Appropriateness Measure (IAM), • Feasibility of Intervention Measure (FIM)

时间窗: Immediately after the VR intervention the scale will be filled in by the participant

Each subscale comprises four elements ranging from 1 (completely disagree) to 5 (completely agree)

User satisfaction

时间窗: Immediately after the VR intervention

NRS score ranging from 0 (not satisfied) to 10 (very satisfied)

次要结局

  • Stress level(immediately before the intervention (pre-intervention) and immediately after the intervention (post-intervention))
  • CSQ-VR(immediately after the VR intervention)
  • Best organizational fit(At a scheduled moment within 1 month after the intervention)

研究者

发起方
Amsterdam UMC, location VUmc
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sophie Vermeulen

Medical doctor, PhD Candidate Department of Surgery

Amsterdam UMC, location VUmc

研究点 (2)

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