跳至主要内容
临床试验/KCT0002696
KCT0002696招募中未知

Safety and effect on shoulder joint of a novel shoulder rehabilitation device

Wonkwang University Hospital0 个研究点目标入组 36 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
36

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
20(Year) 至 80(Year)(—)
性别
All

入选标准

  • Subacute stroke patients who reported hemiplegic shoulder pain with a minimum visual analogue scale (VAS) of 3 points (0-10 point scale) were recruited for 12 months consecutively from July, 2016.

排除标准

  • 1) significant cognitive impairment (Korean version of Mini-Mental State Examination, K-MMSE <15) or language deficits that might affect the reliability of responses to outcome measure scales, 2) pre-existing shoulder pain prior to stroke, and 3) definite shoulder dislocation of affected limb as seen on radiographs due to safety concern.

研究者

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