跳至主要内容
临床试验/NCT01225120
NCT01225120Unknown不适用

Amputee Gait Training Using Virtual Reality and Real-Time Feedback

Brooke Army Medical Center2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2007年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
66
试验地点
2
主要终点
Gait Biomechanics

研究概览

简要总结

The purpose of this repeated measures design gait training study is to develop and quantitatively assess the effectiveness of a virtual reality training environment using real-time feedback for modification of pelvic motion during gait.

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
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Unilateral traumatic trans-tibial or transfemoral amputation
  • Independent ambulation without an assistive device for a minimum of three months
  • Ability to ambulate continuously for a minimum of 15 minutes
  • Trans-femoral participants must use an ischial containment socket
  • VAS Pain scores on the involved side of less than 4/10
  • Sagittal plane ankle, knee and hip strength of 4 or greater on the uninvolved side as determined by manual muscle test.

排除标准

  • Blindness
  • TBI-Glascow Coma Scale score of 12 or lower at the time of injury
  • Cardiac or pulmonary problems limiting physical activity
  • PTSD or other psychological condition with symptoms that would be exacerbated by participation in the study.

结局指标

主要结局

Gait Biomechanics

时间窗: 3 weeks from initial post training

次要结局

未报告次要终点

研究者

申办方类型
Fed

研究点 (2)

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