跳至主要内容
临床试验/NCT05194254
NCT05194254招募中不适用

MRI-Eye Tracking Pairing, a Tool for Assessing Social Cognition in Children With ASD

Centre Hospitalier Universitaire, Amiens1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2022年1月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
68
试验地点
1
主要终点
difference of mapping IRM-ET results between both patient groups

研究概览

简要总结

Most studies use static visual percepts that are less representative of joint attention versus an ecological environment. This has the consequence of decreasing the perception of an interaction with a social partner, which is an essential step in achieving joint attention. The originality of this study is to improve the design of visual percepts (in the form of video) in order to mimic an ecological environment as much as possible by using MRI-ET coupling. The second originality of this study is the longitudinal exploration of the neurodevelopment of social cognition in autistic children. Studies by the Redcay and Oberwelland teams observe different activations at different ages. The hypothesis is that the perception of joint attention varies over time in people with ASD. To date, there are no studies to determine the influence of childhood neurodevelopment in autistic people on the perception of joint attention. It would be unprecedented to use the MRI-ET pairing as a tool for assessing social cognition as a function of the development of children with ASD.

研究设计

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

入排标准

年龄范围
10 Years 至 20 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •For the group of people with Autism Spectrum Disorders (experimental group):
  • •Age between 10 to 20 years old
  • •Diagnosis of ASD (CARS) ≥ 30 performed at inclusion
  • •IQ test evaluation (regardless of the result) performed by a trained psychologist
  • •Obtaining informed oral and written consent after appropriate information
  • •Obtaining informed oral and written consent from the legal guardian after information
  • •Be affiliated with social security
  • •No contraindication to magnetic resonance imaging
  • •For the TD (Typical Development) group of people (control group):
  • •Age between 10 to 20 years old
  • •Diagnosis of ASD (CARS) <30 performed at inclusion
  • •IQ test evaluation (regardless of the result) performed by a trained psychologist
  • •Obtaining informed oral and written consent after appropriate information
  • •Obtaining informed oral and written consent from the legal guardian after information
  • •Be affiliated with social security
  • •No contraindication to magnetic resonance imaging

排除标准

  • •For all groups:
  • •Age outside the range 10 to 20 years
  • •Person with a contraindication to MRI (including claustrophobia, pace maker, neurosurgical clips, vascular clips, heart valves, ventriculoperitoneal valves, cochlear implant, neurostimulator, intraocular metal shards, joint prosthesis, etc.)
  • •Person suffering from major obesity (> 140 kg) not allowing him to enter the tunnel of the MRI machine (diameter <70cm)
  • •Pregnant or breastfeeding woman
  • •Person under guardianship or guardianship or deprived of liberty by a judicial or administrative decision
  • •For TD people (control group):
  • •Person with psychiatric disorders such as attention disorder with or without hyperactivity, depression, bipolar disorder and schizophrenia.
  • •Person with a neurological history such as epilepsy and / or neurovascular accident.

研究组 & 干预措施

ASD

Experimental

people with Autism Spectrum Disorders

干预措施: MRI-ET (Other)

TD

Active Comparator

Typical Development) group of people

干预措施: MRI-ET (Other)

结局指标

主要结局

difference of mapping IRM-ET results between both patient groups

时间窗: one day

both patient groups are : the group of people with Autism Spectrum Disorders and Typical Development group of people

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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