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临床试验/NCT04920461
NCT04920461Unknown不适用

Visual-spatial and Visual-perceptual Disorders Following Cerebellar Strokes

Centre Hospitalier Universitaire de Besancon1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2020年4月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
42
试验地点
1
主要终点
Presence of Neuro-Visual Disorder

研究概览

简要总结

This study aims at assessing the proportion of patients suffering from neuro-visual troubles (visual-spatial and/or visual-perceptual ), after cerebellar strokes.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Signed informed consent form
  • •Being able to pass initial neuropsychological tests within 10 days after stroke

排除标准

  • •Previous central neural system/psychiatric/eye disease (including severe cranial trauma)
  • •Chronic alcoholism
  • •MRI contraindication.

研究组 & 干预措施

Additional MRI sequences

Experimental

干预措施: Additional MRI sequences (Device)

Additional MRI sequences

Experimental

干预措施: Neuropsychological assessment (Other)

结局指标

主要结局

Presence of Neuro-Visual Disorder

时间窗: Month 3

Presence of neuro-visual disorder will be confirmed by obtaining at least 2 pathological scores at following neuropsychological tests: * Rey \& Taylor figures (score from 0 to 36, maximum) * Judgment of Line Orientation (score from 0 to 36, maximum) * Weschler Adult Intelligence Scale (final score is intelligence quotient, with an average score is fixed at 100) * Test of Attentional Performance * Visual Object and Space Perception Battery (eight tests each designed to assess a particular aspect of object or space perception, while minimising the involvement of other cognitive skills) * Visual agnosia assesment protocole (noted on 10 points)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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