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临床试验/NCT03100422
NCT03100422已完成不适用

Strategies of Therapy With the Exoskeleton Robot ARMinMulti VIT-ARMin

Swiss Federal Institute of Technology2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2017年5月1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
18
试验地点
2
主要终点
Fugl Meyer Assessment, upper extremity motor function

研究概览

简要总结

Neurological patients (e.g., after stroke) need long-term neurorehabilitation therapy of the arm with often limited, unsatisfactory outcome. Robots became a promising supplement or even alternative for neurorehabilitation training.

详细描述

The exoskeleton robot ARMin was further developed and software components adapted accordingly to offer a unique intensified and patient-tailored robot-aided training of the arm. The goal is to enhance treatment efficacy to an extent that the improvement in motor function is meaningful for the individual patient. The study objective is to compare ARMin therapy and a form of conventional occupational therapy that involves both arms regarding change in motor function.

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
Double (Investigator, Outcomes Assessor)

盲法说明

Lots will be drawn that assign to either robotic therapy or occupational therapy

入排标准

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

入选标准

  • - Aged ≥18 years
  • Ischemic cerebral vascular accident (CVA, stroke) in the sub-acute phase (one to twelve weeks post-stroke) as verified by brain imaging (CT or MRI)
  • Inpatient at Rehaklinik Zihlschlacht, Switzerland
  • Decreased arm motor function in one arm with a FMA of 8 to 20 points (out of 66)
  • No excessive spasticity of the affected arm (modified Ashworth Scale mAS ≤3) as assessed by the physician
  • No serious medical or psychiatric disorder as assessed by the physician
  • No serious orthopaedic, rheumatologic or other disease restricting movements of the paretic arm as assessed by the physician
  • No clinically significant shoulder subluxation (palpation <2 fingers) as assessed by the physician
  • No skin ulcerations at the paretic arm as assessed by the physician
  • Ability to communicate effectively with the examiner such that the validity of the patient's data could not be compromised as assessed by the physician
  • No history of cyber sickness (e.g., nausea when looking at a screen or playing computer games) as assessed by the physician
  • No pacemaker or other implanted electric device as verified by patient record
  • Bodyweight <120 kg
  • No serious cognitive defects or aphasia preventing effective use of ARMin as assessed by the physician

排除标准

  • 未提供

结局指标

主要结局

Fugl Meyer Assessment, upper extremity motor function

时间窗: from baseline to day 3 post-training

impairment based clinical test

次要结局

  • Motor Activity Log(from baseline to day 3 post-training)
  • handheld dynamometer(from baseline to day 3 post-training)
  • ARMin assessment time(from baseline to day 3 post-training)
  • ARMin assessment torques(from baseline to day 3 post-training)
  • Intrinsic Motivation Inventory(from baseline to day 3 post-training)
  • ARMin assessment positions(from baseline to day 3 post-training)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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