跳至主要内容
临床试验/NCT01225432
NCT01225432Unknown不适用

The Effect of Gait Training Using Virtual Reality and Real-Time Feedback on Physiological and Functional Gait Performance in Persons With a Traumatic Lower Extremity Amputation

Brooke Army Medical Center1 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1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
66
试验地点
1
主要终点
Gait Oxygen Consumption

研究概览

简要总结

To assess the carryover effect of an innovative new gait training program on physiological and functional gait performance in persons with a traumatic lower extremity amputation. A second objective is to clarify the relationship between gait biomechanics (joint and sgment kinematics and energy cost.

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.

研究组 & 干预措施

Gait Training

Experimental

干预措施: Gait Training (Other)

结局指标

主要结局

Gait Oxygen Consumption

时间窗: 3 weeks later from first post training testing

Gait Oxygen Consumption

时间窗: Immediately prior to start of 3 week training.

Gait Oxygen Consumption

时间窗: Immediately post training

Gait Oxygen Consumption

时间窗: 3 weeks

次要结局

未报告次要终点

研究者

申办方类型
Fed

研究点 (1)

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