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临床试验/NCT07349563
NCT07349563已完成不适用

Effect of Nature-Based Virtual Reality and Two-Dimensional Nature Videos on OSCE-Related Exam Stress in Nursing Students: A Randomized Controlled Trial

Acibadem University0 个研究点目标入组 60 人开始时间: 2025年12月2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

Objective Structured Clinical Examinations (OSCEs) are widely used in nursing education to assess clinical skills but are known to induce significant psychological and physiological stress due to performance anxiety, time pressure, and observation. Exam-related stress has been associated with changes in heart rate variability (HRV), particularly increased low-frequency/high-frequency (LF/HF) ratios, reflecting heightened sympathetic activity. Such stress may negatively affect cognitive performance, clinical competence, and professional readiness.

Nature-based virtual reality (VR) has emerged as a promising intervention for stress reduction by providing immersive, calming environments that promote relaxation and autonomic regulation. Previous studies suggest that short VR-based nature sessions can effectively reduce anxiety and may be more effective than two-dimensional (2D) nature videos, which represent a more accessible but less immersive alternative. However, evidence regarding the use of VR and 2D nature videos for managing stress during high-stakes clinical examinations such as OSCEs is limited.

This randomized controlled study aims to compare the effectiveness of nature-based VR and 2D nature videos in reducing OSCE-related stress among third-year nursing students using physiological (PPG-derived LF/HF ratio) and subjective (STAI and SUD) outcome measures.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Undergraduate third-year nursing students scheduled to take the final OSCE examination.
  • Aged between 18 and 25 years.
  • Considered healthy, with no known cardiovascular disease or chronic stress-related disorders.
  • Willing to participate in the virtual reality or 2D nature video intervention.
  • Able to understand the study procedures and provide written informed consent.

排除标准

  • Known sensitivity or intolerance to virtual reality, including symptoms such as dizziness, nausea, headache, or visual discomfort.
  • Medical conditions that may affect photoplethysmography (PPG) measurements, such as cardiac arrhythmias or significant skin sensitivity at the measurement site.
  • Use of medications that may influence heart rate variability, including beta-blockers.
  • Inability to allocate sufficient time to participate in the pre-examination stress management intervention.
  • Pregnancy, acute illness, or current use of psychiatric medications.
  • Refusal to participate or failure to provide informed consent.

研究者

发起方
Acibadem University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Güzin Ünlü Suvari

Lecturer

Acibadem University

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