NCT02098135已完成不适用
Phase 1 Study of a Home Therapy and Assessment for Patients With Arm Impairments
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 14
- 试验地点
- 1
- 主要终点
- Numbers of participant which can perform the ArmeoSenso - training.
研究概览
简要总结
stroke, spinal cord injury, rehabilitation, home therapy, upper limb, arm, virtual reality, interia sensor,
- Trial with medical device
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •18 years old
- •Stroke or spinal cord injury in prehistory
- •Motor deficits of the upper limb (s)
- •Lifting the paretic arm against gravity possible AND
- •Minimum amount of movement in the horizontal plane of 20 x 20 cm
- •Ability and willingness to participate in the study
排除标准
- •Severe aphasia
- •Severe dementia
- •Severe depression
- •Relevant restriction of vision, which can not be compensated by aids (eg hemianopia)
研究组 & 干预措施
ArmeoSenso
Experimental
The ArmeoSenso system is an easy to set up and use upper limb rehabilitation system for the home environment. It consists of a motion capture system based on wearable sensors in combination with a personal computer as well as a therapy software that provides an ergonomic user interface, therapy games and automated assessments.
干预措施: ArmeoSenso (Device)
结局指标
主要结局
Numbers of participant which can perform the ArmeoSenso - training.
时间窗: 42 days
次要结局
- Improvement in the Arm function(42 days)
研究者
研究点 (1)
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