Treatment of Parental Anxiety With Virtual Reality (VR): A Prospective, Randomized Study
概览
- 阶段
- 不适用
- 干预措施
- Control
- 疾病 / 适应症
- Anxiety
- 发起方
- Stanford University
- 入组人数
- 485
- 试验地点
- 1
- 主要终点
- Anxiety levels
- 状态
- 已完成
- 最后更新
- 2个月前
概览
简要总结
The purpose of this study is to determine if non-invasive distracting devices (Virtual Reality headset) are more effective than the standard of care (i.e., no technology based distraction) for preventing anxiety in parental and pediatric populations
研究者
Thomas Caruso
Clinical Professor
Stanford University
入排标准
入选标准
- •Ages 18-99 (Parents whose children is hospitalized)
- •Able to consent
- •Parents whose child is undergoing various procedures at LPCH and Stanford Hospital and Clinics.
排除标准
- •People who do not consent
- •Significant Cognitive Impairment
- •History of Severe Motion Sickness
- •Current Nausea
- •Visual Problems
- •Patients whose children are clinically unstable or require urgent/emergent intervention
研究组 & 干预措施
Control
No intervention (i.e. virtual reality headset) will be applied to the participant.
Virtual Reality
Participants will be immersed in a virtual environment. Calming scenery will be shown via the headset for 20-30 minutes
干预措施: Virtual Reality headset with calming scenery
结局指标
主要结局
Anxiety levels
时间窗: immediately after the intervention
Anxiety level measured by a Visual Analogue Scale - Anxiety (VAS-A) ranging from 0-10. Scale ranges from 0-10, with higher scores indicating higher anxiety levels.
次要结局
- State-Trait Anxiety Inventory(baseline, immediately after the intervention)
- Modified Pain Catastrophizing Scale(immediately after intervention)
- Device satisfaction(immediately after intervention)
- Procedural-Related Anxiety(Duration of intervention, approximately 20-30 minutes)