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临床试验/NCT03004144
NCT03004144已完成不适用

Impact of Robotic Assistive Forces on the Performance of Activities of Daily Living

University of Zurich2 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2016年10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
65
试验地点
2
主要终点
3-dimensional kinematic analyses resulting in a detailed movement profile for each of the performed tasks

研究概览

简要总结

This study is a cross-sectional study investigating the impact of assistive forces applied by the body-weight support system "the FLOAT" on the study participants. The study is conducted at the University Hospital Balgrist in Zurich over a period of around 3 years. During this time measurements on approximately 140 able bodied subjects and 60 patients with an incomplete spinal cord injury will take place. The study participants are invited for a single visit of around 140 min duration to the University Hospital Balgrist. During this visit the study participants will repeatedly perform various activities of daily living (free walking, standing up and sitting down, stair climbing and balancing) with and without assistive forces from the body-weight support system. While performing the tasks, the study participants' motions and muscle activities will be measured to evaluate the naturalness of their movements. In addition, the collected data permits us to compare different movement patterns and make conclusions about effective and optimal movement support. Obtaining this knowledge will help us to shape the therapy of these activities to be tailored to the patients and to train these movements with the help of the FLOAT under optimal 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
Basic Science
盲法
None

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

  • Individuals with incomplete spinal cord injury (AIS C-D) or able bodied persons
  • informed consent as documented by signature
  • bodyweight < 120 kg

排除标准

  • a significant psychiatric or orthopedic diagnose
  • any secondary neurological complications that may impact the outcome variables
  • dermatological conditions (pressure ulcers, etc.)
  • pacemaker or other implanted, electronic devices
  • contraindications for FLOAT training
  • inability or unwillingness to provide written informed consent or follow study procedures e.g. due to language problems
  • psychological disorders, dementia, etc.
  • known or suspected non-compliance, drug or alcohol abuse
  • enrolment of the investigator, his/her family members, employees and other dependent persons

结局指标

主要结局

3-dimensional kinematic analyses resulting in a detailed movement profile for each of the performed tasks

时间窗: Once (single visit) around 140 minutes duration

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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