Virtual Reality to Reduce Anxiety, Agitation and Delirium in Critically Ill Patients
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Feasibility of Intervention Measure (FIM)
研究概览
简要总结
This is a pilot feasibility study examining the use of immersive virtual reality (VR) in adult intensive care unit (ICU) patients. The study evaluates whether brief, non-interactive VR sessions delivered using a commercially available standalone head-mounted display with calming, nature-based content can be delivered safely and effectively within routine SICU workflow. Exploratory objectives assess whether VR sessions are associated with changes in anxiety, agitation, delirium, pain, and sedative medication requirements. This research is not intended to evaluate the safety or effectiveness of the headset and/or the specific VR software used for the research
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Aged ≥ 18 years old admitted to the Surgical Intensive Care Unit (SICU) at Penn State Health Milton S. Hershey Medical Center.
- •No significant uncorrectable visual or auditory impairments
- •Estimated ICU length of stay > 48h
- •At the time of each VR session, able to keep eyes open for at least 30 seconds, follow simple commands and able to indicate discomfort or request to stop.
- •English speaking
排除标准
- •Significant hemodynamic instability
- •Known psychotic disorders associated with delusions (e.g. schizophrenia)
- •Severe dementia (e.g. inability to communicate or follow simple commands)
- •History of disequilibrium syndrome or vertigo
- •Acute hyperactive delirium, requiring physical restraints
研究组 & 干预措施
VR Intervention
Critically ill patients
干预措施: Virtual reality (VR) therapy (Behavioral)
结局指标
主要结局
Feasibility of Intervention Measure (FIM)
时间窗: From time of enrollment to end of intervention at 3 days
Acceptability of Intervention Measure (AIM)
时间窗: From time of enrollment to end of intervention at 3 days
Intervention Appropriateness Measure (IAM)
时间窗: From time of enrollment to end of intervention at 3 days
次要结局
未报告次要终点
研究者
Pauline Go
Principal Investigator
Milton S. Hershey Medical Center