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临床试验/NCT01936298
NCT01936298已完成不适用

Robot-assisted Rehabilitation of Hand by Paralysis of the Upper Limb After Stroke

Chiara Mulé2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2013年9月1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
35
试验地点
2
主要终点
Change from Baseline of Perimeter edema

研究概览

简要总结

The investigators evaluate the effectiveness of the application of continuous passive motion device for hand rehabilitation in two classes of patients: with a residual active motion and without a residual active motion.

详细描述

We will conduct a double blind clinical trial. A sample size calculation were performed to determine the necessary number of subjects needed for this study and was based upon the results of a previous pilot study. All patients had functional impairments of their upper extremities after the stroke.

We hypothesized that the hand-rehabilitation oriented with robotics assistance, would improve edema by paralysis of the upper limb even in patient without sensory pathway recovery.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • a history of acute phase of stroke (less than 12 months post onset),
  • first stroke episode,
  • no history of peripheral nerve injury or musculoskeletal disease in the affected upper extremity,
  • no contracture of the affected wrist or fingers (Modified Ashworth<3),
  • no history of any invasive procedure (Botulinum toxin type A) for the treatment of spasticity for at least 6 months before the start of this study,
  • for P-ROM patients, the absence of active hand movements,
  • for the A-ROM patients, the presence of active hand movements.

排除标准

  • unstable medical disorders,
  • active Complex Regional Pain Syndrome (CRPS),
  • severe spatial neglect,
  • cognitive problems.

结局指标

主要结局

Change from Baseline of Perimeter edema

时间窗: 1 day after the treatment

次要结局

  • Change from Baseline of Visual analogue scale (VAS)(1 day after the treatment)
  • Change from Baseline of Modified Ashworth Scale for Grading Spasticity (MAS)(1 day after the treatment)
  • Change from Baseline of Range Of Motion (ROM)(1 day after the treatment)
  • Clinical Global Impression (CGI)(1 day after the treatment)

研究者

发起方
Chiara Mulé
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Chiara Mulé

Physiatrist Physician

Habilita, Ospedale di Sarnico

研究点 (2)

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