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临床试验/NCT02938754
NCT02938754已完成不适用

Motor and Cognitive Training With the Rehabilitation Gaming System for Patients Affected by Cerebral Palsy

Universitat Pompeu Fabra2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2016年11月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
2
主要终点
Change in motor function of the affected extremity as measured by MACS clinical scale

研究概览

简要总结

In this study the investigators evaluate the effectivity of Virtual Reality-based rehabilitation protocols for preventing motor deterioration in patients with cerebral palsy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
12 Years 至 50 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Children and Adult patients between 12- 50 years old diagnosed with CP according to Gross Motor Function Classification System (GMFCS). Level of disability between I and IV.
  • Ashworth modified clinical scale < 3 (Ashworth, 1964, Bohannon Bohannon and Smith, 1987).

排除标准

  • Severe visual impairment.
  • Severe cognitive impairment such as mental retardation which impedes the understanding of the task.

研究组 & 干预措施

VR-based motor training

Experimental

Subjects will perform 3 different training protocols in Virtual Reality that imply performing tasks of vertical and planar reaching and hitting spheres, or hockey pucks, spaced at different time, speed and color.

干预措施: VR-based motor training (Behavioral)

Conventional Therapy

Active Comparator

Subjects will perform conventional rehabilitation tasks for the upper-extremities that imply vertical and planar reaching movements.

干预措施: Conventional Therapy (Behavioral)

结局指标

主要结局

Change in motor function of the affected extremity as measured by MACS clinical scale

时间窗: Change from Baseline to week 5 (End of Treatment)

次要结局

  • Change in motor function of the affected extremity as measured by the Box and Blocks clinical scale(Change from Baseline to week 5 (End of Treatment))
  • Change in the amount of use of the affected arm during training as measured by the Virtual Reality system(Change from Baseline to week 5 (End of Treatment))
  • Change in attention and visuo-perceptive and visuo-constructional apraxia as measured by the WAIS-III scale(Change from Baseline to week 5 (End of Treatment))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paul Verschure

PhD

Universitat Pompeu Fabra

研究点 (2)

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