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临床试验/ACTRN12608000457347
ACTRN12608000457347招募中未知

To investigate in stroke survivors undergoing inpatient rehabilitation, the degree of recovery of upper limb motor function that accrues from (A) usual care vs. (B) a non-robotic device (SMART Arm) alone + usual care vs. (C) SMART Arm with triggered electrical stimulation + usual care.

The University of Queensland0 个研究点目标入组 75 人开始时间: 2008年9月15日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
75

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
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Individuals will be included if they: have a diagnosis of first ever stroke which occurred within 3mths of the initial test date, be unable to independently perform a standardised reaching task, and be admitted to the Princess Alexandra Hospital (PAH) or QEII hospitals, Brisbane Australia.

排除标准

  • Individuals will be excluded if they have co-morbidities relating to the upper extremity that limit function, such as arthritis, brain injury, Parkinson disease or are unable to tolerate stimulation (e.g. due to hypersensitivity or a skin condition); if they are medically unstable; or are unable to understand the instructions or provide informed consent.

研究者

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