Contribution of Virtual Reality to the Well-being of Elderly Patients Hospitalized in SMR
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 主要终点
- WHO-5
研究概览
简要总结
The objective of this clinical trial is to evaluate the effect of using virtual reality on the well-being of elderly patients hospitalized in SMR for 3 weeks. The study also allows to evaluate the effect of VR on apathy, and the autonomy of patients hospitalized in the SMR department for 3 weeks.
详细描述
Patients meeting the inclusion criteria and agreeing to participate in the study will be enrolled and then randomized to either the VR immersion group or the control group. Patients included in the protocol will not undergo any changes to their care. Patients in the experimental group will receive 12 virtual reality sessions in addition to their usual care.
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
- 70 Years 至 —（Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •People hospitalized in the SMR unit at La Porte Verte Hospital for a minimum of 3 weeks,
- •People with preserved or slightly impaired cognitive status with an MMSE ≥ 20,
- •People who have been informed and have signed written informed consent
排除标准
- •People under guardianship or curatorship,
- •People with difficulty understanding the VR study and materials,
- •People with vision problems that impact the use of VR,
- •People with hearing problems that impact the use of VR,
- •People with epilepsy,
- •People at risk of nausea and dizziness when using the VR headset,
- •People who cannot tolerate the VR headset,
- •Not affiliated with a social security scheme.
- •People receiving care with reflexology and relaxation massage
研究组 & 干预措施
VR group
干预措施: Virtual Reality (Other)
contrrol arm
结局指标
主要结局
WHO-5
时间窗: 4 times throughout of study at baseline and after each VR session
measure well-being. The score is between 0-100 a high score means better wellness
次要结局
未报告次要终点