跳至主要内容
临床试验/NCT04279158
NCT04279158招募中不适用

Attention Modulation of Local and Global Inhibition Mechanisms

Hospices Civils de Lyon2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2022年11月26日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
2
主要终点
error rate

研究概览

简要总结

Human behavior is both flexible and adapted to the environmental context through inhibition capabilities; the investigator control the subject's behavior by repressing inappropriate responses and selecting, among several possibilities, those that are appropriate. These mechanisms are not independent of attentional control. Attention acts as a selection filter for the investigator's behavior. This leads us to hypothesize that attention modulates the mechanisms of inhibition. Nevertheless, the different brain structures involved, as well as mechanisms underlying the interaction between inhibition and attention remain largely unknown.

Previous research has suggested that inhibition requires selective attention and, conversely, attentional mechanisms would result in the "deselection", or inhibition, of objects in space or irrelevant actions. Reconciling the literature on attention with the one on inhibition appears fundamental for the understanding of the instance to which the mechanisms of inhibition and the cognitive processes interact. Therefore, the goal of this research project will be to investigate how inhibition mechanisms are implemented in the brain and, in more detail, what determines the type of resulting inhibitory control: spatially localized or global. The investigator will test 3 different patient groups (optic ataxia, hemispatial neglect and attention-deficit hyperactivity disorder) compared to control.

In conclusion, this research project will aim to develop a theoretical model of the interaction between attentional control and inhibition mechanisms in order to improve diagnostic and rehabilitation tools in the future.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
8 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients and healthy subjects:
  • Inclusion Criteria:
  • male and female, age from 18 to 75 years included
  • normal vision or corrected vision
  • covered by social security
  • signed written informed consent

排除标准

  • unable to comply with requirements of the study (neurological, psychiatric, sensory or motor troubles)
  • adults under legal protection
  • Patient with hemispatial neglect:
  • Inclusion Criteria:
  • After a stroke (> 1 month ago), presence of a neurological impairment documented by brain imaging (standard of care) and by clinical symptoms.
  • The diagnosis will be dissociated from hemianopia by perimetry. The hemispatial neglect consists of a lack of perception and responsiveness concerning the controlesional visual hemifield.
  • Patient with optic ataxia:
  • After a stroke (> 1 month ago), presence of neurological injury in parietal cortex only, supported by a standard of care cerebral MRI
  • Present optic ataxia symptoms (The OA consists of pointing errors with the hand contralateral to the lesion (hand effect) and / or to visual targets presented in the field contralateral to the lesion (field effect)).
  • Patient (adult and children) with attention-deficit hyperactivity disorder:
  • present a diagnosis of ADHD subtype inattention or impulse / hyperactivity as established by a neuropsychologist.
  • Children will be between 8 and 18 years old
  • Adults will be between 18 and 75 years old.
  • Participants will not report any comorbid learning disabilities to ADHD.
  • For minors:
  • - Having obtained the written consent of the legal representative(s)
  • Healthy subjects
  • Inclusion Criteria:
  • - no known neurological injury

结局指标

主要结局

error rate

时间窗: at the end of the simulation passage, an average of 3 years

The investigator calculate the number of right and wrong answers (a correct answer is a saccade carried out when it is necessary and by reaching the target; a false answer is a saccade made at the wrong time and / or not reaching the target) to obtain the error rate.

次要结局

  • reaction time(at the end of the simulation passage, an average of 3 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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