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临床试验/KCT0007230
KCT0007230尚未招募未知

Comparative analysis study on passive and active robotic devices to change arm functionality through proximal upper extremity assistance in patients with spinal cord injury

ational Rehabilitation Center0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19?(Year) 至 o Limit(—)
性别
All

入选标准

  • 1. Chronic patients more than 3 months after onset
  • 2. Tetraplegia patients (C2-T1)
  • 3. A patient with weakness in the muscle strength of the proximal part of the upper extremity.
  • 4. If the proximal part of the upper extremity is good, endurance is low, and there is a limitation in performing daily activities such as eating and grooming.
  • 5. Patients with shoulder and elbow range of motion of more than 90 degrees and 50 degrees, respectively.
  • 6. Those who can sit tolerance for more than 30 minutes.

排除标准

  • 1. Those with severe contracture problems in the upper extremities
  • 2. Patients with obvious diseases that can cause muscle weakness due to abnormalities in the central nervous system other than spinal cord injury (eg, neuromyalgia)
  • 3. Those who have difficulty following the therapist's instructions due to cognitive problems.
  • 4. Those who have limited upper extremity movement due to stiffness of MAS 3 or higher
  • 5. A person who can independently carry out daily life activities

研究者

发起方
ational Rehabilitation Center

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