Evaluation of the Performance of VRP-Clinic in Healthy Subjects in the Support of Rehabilitation
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 20
- 试验地点
- 2
- 主要终点
- Number of VRP-Clinic Neck Movements That the Assessing Clinician Recognizes as Rehabilitation Movements
研究概览
简要总结
The current study is designed to evaluate neck movements performed according to the VRP-Clinic software, and to verify that they promote physical activities that correspond with physical rehabilitation.
详细描述
The study will take place at Shaare Zedek Medical Center (SZMC). The study will include a single visit.
Each subject will put on the VR headset and perform a series of neck movements guided by graphic instructions appearing in the VR environment. The session will be recorded with a video camera which will subsequently be viewed and evaluated by clinicians. The clinicians will identify each movement seen on the video from a predefined list and determine if such a movement is recommended as part of a rehabilitation training program.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy male or female
排除标准
- •History of neck related disorders (Whiplash, disc degeneration disease or other acute cervical spine conditions)
- •Current neck pain
- •Under medical treatment or observation for any health-related issue during the study
- •Recent trauma
- •Oncology background
- •Acute disease/illness
- •Using drugs that could potentially affect physical function and balance (such as corticosteroids, antipsychotics or antidepressants)
- •Vision problems that require glasses (not all frame types can fit into the headset)
研究组 & 干预措施
VRP-Clinic
VRP-Clinic software on a virtual reality platform
干预措施: VRP-Clinic (Other)
结局指标
主要结局
Number of VRP-Clinic Neck Movements That the Assessing Clinician Recognizes as Rehabilitation Movements
时间窗: Up to 2 weeks after the session
The movements are recorded on video and sent to clinicians for evaluation after the session is completed. The movements are then evaluated by the clinicians according to a predetermined list.
次要结局
- Number of Participants With Any Adverse Event Occurring During the Study(through study completion, an average of 2 weeks)