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临床试验/NCT03203772
NCT03203772已完成不适用

Management of Pain in Limb Neuropathic Conditions Through Immersive Virtual Reality

Loma Linda University2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2016年8月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
2
主要终点
Pain Relief with Virtual Reality Therapy: Visual Analog Scale

研究概览

简要总结

Investigating how neuropathic limb pain, including phantom limb pain or complex regional pain syndrome, is affected by virtual reality. While several studies have looked into virtual reality for treating this type of pain, few have used the latest immersive virtual reality hardware combined with motion control for an engaging virtual mirror therapy experience. The investigators are interested in studying the use of virtual reality as an alternative treatment option for these conditions.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of complex regional pain syndrome or phantom limb pain in an upper or lower limb

排除标准

  • Cognitive impairment leading to inability to make own medical decisions
  • Complete inability to utilize leg or arm muscles that are needed for motion controller tracking
  • History of seizures within the last year

结局指标

主要结局

Pain Relief with Virtual Reality Therapy: Visual Analog Scale

时间窗: Change from initial scores prior to virtual reality exposure to immediately prior to and following virtual reality sessions, and up to 8 weeks following last sessions

Change in Visual Analog Pain Scale will be measured. This will be done by obtaining pain scale scores immediately prior to therapy session, immediately following therapy, and several weeks post last therapy session.

Pain Relief with Virtual Reality Therapy: Short-Form McGill Pain Scale

时间窗: Change from initial scores prior to virtual reality exposure to immediately prior to and following virtual reality sessions, and up to 8 weeks following last sessions

Change in Short-Form McGill Pain Questionnaire will be measured. This will be done by obtaining pain scale scores immediately prior to therapy session, immediately following therapy, and several weeks post last therapy session.

Feasibility of Virtual Reality Environment Use Questionnaire

时间窗: Immediately following final virtual reality session

Using a questionnaire, feedback over participant self-reported tolerance of the virtual reality environment, participant likelihood of recommending this therapy to others with similar conditions, reported sense of presence in presented scenario(s), comfort of virtual reality devices, impact on self-reported functional ability outside of clinic, and overall impression of virtual reality therapy will be recorded.

Pain Relief with Virtual Reality Therapy: Wong-Baker Scale

时间窗: Change from initial scores prior to virtual reality exposure to immediately prior to and following virtual reality sessions, and up to 8 weeks following last sessions

Change in Wong-Baker Faces pain scale will be measured. This will be done by obtaining pain scale scores immediately prior to therapy session, immediately following therapy, and several weeks post last therapy session.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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