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临床试验/ACTRN12613000132741
ACTRN12613000132741已完成不适用

Clinical research of Intelligent Stroke Rehabilitation System for upper-limb Impairment after stroke in cerebral infarction patients with severe upper-limb impairment

Philips Research Asia, Shanghai(PRAS)0 个研究点目标入组 26 人开始时间: 2013年2月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
26

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Educational / counselling / training

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • within 3 months of the first time onset of cerebral infarction
  • >= 18 years old
  • brain unilateral lesions focused in the middle cerebral artery, confirmed by CT or MRI
  • obvious unilateral hemiplegia: severe motor dysfunction in upper extremity, proximal Fugl-Meyer subscore (FM-prox, 0 to 46) 6–13, lower extremity Brunnstrom classification <= 4
  • With normal language understanding and cognitive function, and capable of signing informed consent and coordinating with the treating program.

排除标准

  • Patients with the following manifestations were excluded: heart, liver, kidney and lung failure, uncontrolled arrhythmia, malignant tumor, musculoskeletal disease significantly affecting the motor function and other neurological disorders, restrictions of upper limb movement, impaired vision, impaired hearing, laterality agnosia and apraxia, impaired cognitive function (Folstein Mini-Mental State Examination, MMSE <22 points), incapable of maintaining sitting homeostasis, serious upper extremity sensory disturbances, severe upper limb joint pain, significant shoulder subluxation, serious upper limb muscle spasms (Modified Ashworth scale = 3), upper limb skin bedsores, and severe hand edema

研究者

发起方
Philips Research Asia, Shanghai(PRAS)

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