跳至主要内容
临床试验/JPRN-jRCTs032200451
JPRN-jRCTs032200451招募中1 期

The Assessment of the unilateral spatial neglect using the immersive VR method in peripersonal space and extrapersonal space

Wada Naoki0 个研究点目标入组 40 人开始时间: 2021年3月31日最近更新:

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 40age old 至 <= 79age old(—)
性别
All

入选标准

  • patient group
  • 1) with ages ranging from 40 to 79.
  • 2) male and female.
  • 3) presence of a first-time right hemisphere stroke (cerebral infarction or cerebral hemorrhage).
  • 4) even if the patients have aphasia, they can understand the instructions and perform the tests.
  • 5) more than 2 weeks after onset and be in a stable condition.
  • 6) can sit independently on chair or in wheelchair.
  • 7) signed informed patients or family consent.
  • healthy group
  • 1) with ages ranging from 40 to 79.
  • 2) male and female.
  • 3) signed informed subjects or family consent.

排除标准

  • patient group
  • 1) a history of major neurological disorders other than stroke.
  • 2) a history of major psychiatric disorders.
  • 3) with head injury.
  • 4) with disturbance of consciousness.
  • 5) with cognitive disorders (the score of Mini-Mental State Examination under 23).
  • 6) presence of visual impairment (e.g. visual field deficit, damage to the optic radiation and the occipital lobe).
  • 7) judged to be unsuitable to the assessment by doctors in the team. The study was approved by the local ethics committee at the hospital, and written informed consent was obtained from all subjects.
  • healthy group
  • 1) a history of major neurological disorders other than stroke.
  • 2) a history of major psychiatric disorders.
  • 3) with head injury.
  • 4) with disturbance of consciousness.
  • 5) with cognitive disorders (the score of Mini-Mental State Examination under 23).
  • 6) presence of visual impairment (e.g. visual field deficit, damage to the optic radiation and the occipital lobe).
  • 7) judged to be unsuitable to the assessment by doctors in the team. The study was approved by the local ethics committee at the hospital, and written informed consent was obtained from all subjects.

研究者

发起方
Wada Naoki

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