AI Article Synopsis

  • The study addresses the need for reliable assessment tools to evaluate early developmental skills in children with neurogenetic syndromes (NGS), suggesting the adaptation of existing measures to improve cost and efficiency.
  • Using Generalizability Theory, the researchers analyzed the reliability of the Communication and Symbolic Behavior Scales-Infant-Toddler Checklist (CSBS-ITC) on 172 children, showing adequate reliability across various NGS groups, especially for Prader-Willi and Williams syndromes.
  • Results indicated differences in error variance between NGS groups and low-risk controls, with the CSBS-ITC providing valuable insights into stability and change in developmental skills.

Article Abstract

Background: The lack of available measures that can reliably characterize early developmental skills in children with neurogenetic syndromes (NGS) poses a significant challenge for research on early development in these populations. Although syndrome-specific measures may sometimes be necessary, a more cost- and time-efficient solution would be to identify existing measures that are appropriate for use in special populations or optimize existing measures to be used in these groups. Reliability is an important metric of psychometric rigor to consider when auditing and optimizing assessment tools for NGS. In this study, we use Generalizability Theory, an extension of classical test theory, as a novel approach for more comprehensively characterizing the reliability of existing measures and making decisions about their use in the field of NGS research.

Methods: We conducted generalizability analyses on a popular early social communication screener, the Communication and Symbolic Behavior Scales-Infant-Toddler Checklist (CSBS-ITC), collected on 172 children (41 Angelman syndrome, 30 Prader-Willi syndrome, 42 Williams syndrome, 59 low-risk controls).

Results: Overall, the CSBS-ITC demonstrated at least adequate reliability in the NGS groups included in this study, particularly for the Prader-Willi and Williams syndrome groups. However, the sources of systematic error variance in the CSBS-ITC varied greatly between the low-risk control and NGS groups. Moreover, as unassessed in previous research, the CSBS-ITC demonstrated substantial differences in variance sources among the NGS groups. Reliability of CSBS-ITC scores was highest when averaging across all measurement points for a given child and was generally similar or better in the NGS groups compared to the low-risk control group.

Conclusions: Our findings suggest that the CSBS-ITC communicates different information about the reliability of stability versus change, in low-risk control and NGS samples, respectively, and that psychometric approaches like Generalizability Theory can provide more complete information about the reliability of existing measures and inform decisions about how measures are used in research on early development in NGS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275516PMC
http://dx.doi.org/10.1186/s11689-020-09318-1DOI Listing

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