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临床试验/NCT02471248
NCT02471248已完成不适用

Interactive Exoskeleton Robot for Walking - Ankle Joint

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2015年5月27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
25
试验地点
1
主要终点
Functional Ambulation Category

研究概览

简要总结

A novel interactive exoskeleton robotic system with embedded force and motion sensors will be developed to facilitate walking of stroke patients with hemiparesis. The robot will synchronise with the gait pattern of the stroke patient to provide assistance in ankle dorsiflexion during swing phase. It is hypothesised that the robot can facilitate stable and longer walking distance for stroke patients with drop foot problem. It can be applied on unilateral side, which is suitable for stroke patients with hemiparesis. The whole system design is lightweight, compact, comfortable, and user-friendly in hospital or at home settings.

详细描述

In this clinical trial, participated stroke patients will be divided into two groups: Robotic group and Sham group. Stroke patients in both groups will participate in a 20-session gait training program, which includes overground walking and stair climbing exercises. Robotic group will walk with the powered Ankle Robot, which provide ankle dorsiflexion support during swing phase of walking; Sham group will walk with the Ankle Robot with very low assistance level, which provide only tactile feedback but no ankle support in order to evaluate the placebo effect. A series of clinical assessments will be carried out to assess the functional recovery in stroke patients before and after the gait training program.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ischemic or hemorrphagic stroke with drop foot problem.
  • Sufficient cognition to follow simple instructions and to understand the content and purpose of the study. (Mini-Mental State Examination > 21)
  • Capable of standing and walking independently for an extended period of time. (Functional Ambulation Category > 3, Berg Balance Scale > 40)

排除标准

  • Any medical or psychological dysfunctions that would affect their ability to comply with test study protocol, such as lower back pain, neuralgia, rotational vertigo, muscloskeletal disorders, injuries, and pregnancy.
  • Any severe contractures in hip, knee, or ankle joint that would preclude passive range of motion in the lower extremity.
  • Participation in any therapeutic treatment ("outside therapy") performed with the lower extremity during the planned study, including the baseline and the follow-up.

结局指标

主要结局

Functional Ambulation Category

时间窗: 3-month follow-up

Assesses postural stability during various walking tasks

6-minute Walk Test

时间窗: 3-month follow-up

Assesses distance walked over 6 minutes as a sub-maximal test of aerobic capacity/endurance

次要结局

  • Berg Balance Scale(3-month follow-up)
  • Fugl-Meyer Assessment of Motor Recovery after Stroke (Lower Extremity)(3-month follow-up)
  • Kinematic and Kinetic Gait Motion Capture(3-month follow-up)
  • Timed 10 Meter Walk Test(3-month follow-up)
  • Modified Ashworth Scale(3-month follow-up)
  • Subjective Feedback Questionnaire(3-month follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Raymond KY Tong

Professor

Chinese University of Hong Kong

研究点 (1)

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