NCT06149468招募中不适用
CAP48 Medical Research Project: Autism Spectrum Disorders in Children and Adolescents
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 500
- 试验地点
- 1
- 主要终点
- Creation of an ADS register
研究概览
简要总结
Evaluation and follow-up of children diagnosed with an autism spectrum disorder in French-speaking Belgium in order to optimize diagnostic protocols, the quality of care required and its accessibility, and to determine the impact of an autism spectrum disorder on schooling, family and society.
详细描述
The aims of the research project:
- To collect a wide range of data in order to improve knowledge of children with autism spectrum disorder (ASD) in French-speaking Belgium by prospectively including all children and adolescents making a request to the centres of reference. The creation of a common database will make it possible to collect general socio-demographic, geographical and epidemiological data, to characterise the different profiles and to accurately monitor developmental trajectories.
- Evaluate the feasibility and practical implementation of the treatment proposed following a diagnosis of ASD in a child.
- Implement protocols to improve the quality of care for beneficiaries.
- To enable the development of fundamental research protocols. Many questions remain unanswered about the genetic, neuro-cognitive and linguistic characteristics of autism. Only rigorous studies carried out on large, carefully defined samples can advance research.
- Increase public knowledge and understanding of the ASD.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- — 至 18 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •children/adolescents (under 18 years of age) who apply to an autism reference center or who are followed up in an autism reference center from French-speaking region of Belgium.
排除标准
- •refusal by the family to allow their child's data to be included in the database.
结局指标
主要结局
Creation of an ADS register
时间窗: Throughout the entire study, approximately during 5 years
creation of a common ASD register to collect general sociodemographic, geographic and epidemiological data, characterize the different patient profiles and accurately track development trajectories
次要结局
- Schooling evaluation(Throughout the entire study, approximately during 5 years)
- Protocols development(Throughout the entire study, approximately during 5 years)
- Feasability assessment(Throughout the entire study, approximately during 5 years)
研究者
研究点 (1)
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