Evidence map›Paper›PMID 32503425›Full record

ArticleJournal of neurodevelopmental disorders2020

Using generalizability theory to evaluate the comparative reliability of developmental measures in neurogenetic syndrome and low-risk populations.

Lisa R Hamrick, Alison M Haney, Bridgette L Kelleher, Sean P Lane

Open access · goldAbstract read
In one paragraph

Article in Journal of neurodevelopmental disorders, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Measurement properties of a patient-reported outcome scale for peptic ulcer: a validation study using classical test theory and generalizability theory.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Lisa R HamrickDepartment of Psychological Sciences, Purdue University, 703 Third Street, West Lafayette, IN, 47907, USA.ORCID 0000-0002-8372-5837
Alison M HaneyDepartment of Psychological Sciences, Purdue University, 703 Third Street, West Lafayette, IN, 47907, USA.
Bridgette L KelleherDepartment of Psychological Sciences, Purdue University, 703 Third Street, West Lafayette, IN, 47907, USA. bkelleher@purdue.edu.
Sean P LaneDepartment of Psychological Sciences, Purdue University, 703 Third Street, West Lafayette, IN, 47907, USA.
Purdue University West Lafayette · US

Funding

Toward a Generalized Framework and Flexible Software Environment for Power Analysis of Alcohol Treatment Randomized Controlled TrialsR01AA027264 · NIAAA · UNIVERSITY OF MISSOURI-COLUMBIA · PI HENNES, ERIN, LANE, SEAN P · 2018 to 2022
$3.4M
Telehealth Assessment of Syndromic Autism Risk in InfantsK23MH111955 · NIMH · PURDUE UNIVERSITY · PI KELLEHER, BRIDGETTE LYNNE · 2017 to 2021
$913k
Analysis of early vocalization features in children at high genetic risk for autismF31DC018219 · NIDCD · PURDUE UNIVERSITY · PI HAMRICK, LISA M · 2019 to 2021
$117k
NIAAA NIH HHS L30 AA027931NIAAA NIH HHS R01 AA027264NIDCD NIH HHS F31 DC018219NIDCD NIH HHS F31DC018219NIMH NIH HHS K23 MH111955NIMH NIH HHS K23MH111955
6 · The paper itself

Abstract

backgroundThe 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.

methodsWe 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).

resultsOverall, 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.

conclusionsOur 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.

Indexed as

Generalization, PsychologicalAnalysis of VarianceAngelman SyndromeChild, PreschoolCommunicationFemaleHumansInfantLongitudinal StudiesMalePrader-Willi SyndromePsychometricsReproducibility of ResultsRiskWilliams SyndromeAngelmanCommunication and Symbolic Behavior ScalesGeneralizability theoryNeurogeneticPrader-WilliReliabilitySocial communicationWilliams

Identifiers

PMID32503425
PMCPMC7275516
OpenAlexW3033938803

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.