缺乏自愿兴趣和难以进行目光接触是 ASQ:SE 中最具辨别力的行为,可能暗示着发育迟缓:大规模评估结果。

IF 1.4 4区 心理学 Q4 CLINICAL NEUROLOGY Applied Neuropsychology: Child Pub Date : 2024-10-01 Epub Date: 2023-01-11 DOI:10.1080/21622965.2022.2156795
Luis Anunciação, Luisa Cito, Luciana Pessoa, Jane Squires, Kimberly Murphy, J Landeira-Fernandez
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引用次数: 0

摘要

背景:每个孩子都是独一无二的,但发育往往是按可预测的步骤和阶段进行的。及早发现面临发育迟缓的婴儿至关重要,这就促进了筛查工具的使用,以确定发育迟缓的风险。里约热内卢市使用年龄与阶段问卷对在教育机构注册的儿童进行了大规模评估:目标:我们研究了ASQ:SE的内部结构及其对12至60个月大儿童发育迟缓风险最具鉴别力的项目。我们利用八个锚定项目的判别参数轨迹来检验它们在整个发育过程中对社会情感能力延迟风险的提示作用:方法:通过项目反应理论(IRT)的 Samejima 分级反应模型分析了 79,332 名儿童(1-5 岁)的数据。计算了区分度(a)和阈值(b)参数,并通过最大似然法求得误差。数据/代码见 https://osf.io/by6sf/.Results:(a) 通过均方根近似误差和标准化均方根残差结果(RMSEA),项目反应理论分析支持数据的单维性。(b) 缺乏自愿兴趣是头 5 年最具区分性的风险行为。(c) 缺乏兴趣是最持久的危险行为。(d) 目光接触困难的信息量几乎与缺乏兴趣的信息量相当:结论:对事物缺乏主动兴趣应被视为与风险有关的重要行为,而眼神交流则是典型发育的重要方面。主要结果:ASQ:SE 是测量儿童发展的有效而可靠的工具。ASQ:SE 的内部结构与单维度解决方案非常吻合,儿童的年龄是 IRT 模型中区分参数的一个重要方面。
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Lack of voluntary interest and difficulty making eye contact are the most discriminative behaviors of the ASQ:SE and might suggest delays: Results from a large-scale assessment.

Background: Every child is unique, but development tends to occur in predictable steps and stages. The early identification of infants who face developmental delays is critical, boosting the use of screening tools to determine risks for delays. The city of Rio de Janeiro conducted a large-scale assessment of children who were enrolled in educational facilities using the Ages & Stages Questionnaires: Social-Emotional (ASQ:SE).

Objectives: We examined the internal structure of the ASQ:SE and its most discriminative items of risks of delays in development among 12- to 60-month-old children. The trajectory of the discrimination parameter of eight anchor items was used to check how well they inform the risk of social-emotional competence delays throughout development.

Methods: Data from 79,332 children (1-5 years) were analyzed via Samejima Graded Response model of Item Response Theory (IRT). The discrimination (a) and threshold (b) parameters were computed, and errors were achieved via maximum likelihood. Data/codes are available at https://osf.io/by6sf/.

Results: (a) Item Response Theory analyses supported the unidimensionality of data via the root mean square error of approximation and standardized root mean square residual results (RMSEA). (b) The lack of voluntary interest was the most discriminative risk behavior in the first 5 years. (c) Lack of interest was the most persistent risk behavior. (d) Difficulty making eye contact was nearly as informative as lack of interest.

Conclusion: Lack of voluntary interest in things should be considered a critical risk-related behavior, and making eye contact is a vital aspect of typical development. Both behaviors may be predictors of children's delays.MAIN OUTCOMESThe ASQ:SE is a valid and reliable tool to measure child development.The internal structure of the ASQ:SE is well-fitted with a unidimensional solution.A child's age is a vital aspect of the discrimination parameter of the IRT model.Lack of interest in things and difficulty making eye contact are critical risk-related behaviors.

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来源期刊
Applied Neuropsychology: Child
Applied Neuropsychology: Child CLINICAL NEUROLOGY-PSYCHOLOGY
CiteScore
4.00
自引率
5.90%
发文量
47
期刊介绍: Applied Neuropsychology: Child publishes clinical neuropsychological articles concerning assessment, brain functioning and neuroimaging, neuropsychological treatment, and rehabilitation in children. Full-length articles and brief communications are included. Case studies of child patients carefully assessing the nature, course, or treatment of clinical neuropsychological dysfunctions in the context of scientific literature, are suitable. Review manuscripts addressing critical issues are encouraged. Preference is given to papers of clinical relevance to others in the field. All submitted manuscripts are subject to initial appraisal by the Editor-in-Chief, and, if found suitable for further considerations are peer reviewed by independent, anonymous expert referees. All peer review is single-blind and submission is online via ScholarOne Manuscripts.
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