Evidence map›Paper›PMID 41364294›Full record

ArticleJournal of patient-reported outcomes2025

Development and initial validation of the Communication Inventory Disability - Observer Reported (CID-OR): a measure of communication in CDKL5 deficiency disorder.

Jenny Downs, Jessica Keeley, Peter Jacoby, Sofia Benson-Goldberg, Sarah Pillar, Andrea Miele, Helen Leonard, Jacinta Saldaris, Eric D Marsh, Tim A Benke and 1 more

Abstract readValidation Study
In one paragraph

Article in Journal of patient-reported outcomes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Jenny DownsThe Kids Research Institute Australia, University of Western Australia, Perth, WA, Australia. Jenny.Downs@thekids.org.au.ORCID http://orcid.org/0000-0001-7358-9037
Jessica KeeleyThe Kids Research Institute Australia, University of Western Australia, Perth, WA, Australia.
Peter JacobyThe Kids Research Institute Australia, University of Western Australia, Perth, WA, Australia.
Sofia Benson-GoldbergSpecial Education and Clinical Sciences Department, College of Education, University of Oregon, Eugene, OR, USA.
Sarah PillarThe Kids Research Institute Australia, University of Western Australia, Perth, WA, Australia.
Andrea MieleDepartment of Pediatrics and Neurology, University of Colorado School of Medicine, Precision Medicine Institute, Children's Hospital Colorado, Aurora, CO, USA.
Helen LeonardThe Kids Research Institute Australia, University of Western Australia, Perth, WA, Australia.
Jacinta SaldarisThe Kids Research Institute Australia, University of Western Australia, Perth, WA, Australia.
Eric D MarshDivision of Neurology, Children's Hospital of Philadelphia, School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Tim A BenkeDepartment of Pediatrics and Neurology, University of Colorado School of Medicine, Children's Hospital Colorado, Aurora, CO, USA.
Scott T DemarestDepartment of Pediatrics and Neurology, University of Colorado School of Medicine, Precision Medicine Institute, Children's Hospital Colorado, Aurora, CO, USA.

Funding

Multi-Site Validation of Biomarkers and Core Clinical Outcome Measures for Clinical Trials Readiness in CDKL5 Deficiency DisorderU01NS114312 · NINDS · UNIVERSITY OF COLORADO DENVER · PI BENKE, TIMOTHY A, DOWNS, JENNY · 2021 to 2025
$4.7M
International Foundation for CDKL5 Research N/ANational Institute of Health U01NS114312NINDS NIH HHS U01 NS114312Stan Perron Charitable Foundation N/A
6 · The paper itself

Abstract

backgroundCDKL5 Deficiency Disorder (CDD) is a rare neurodevelopmental disorder characterised by early onset seizures combined with complex healthcare needs and developmental impairment that influence functional domains including communication. Communication is a high priority domain for families but currently used measures demonstrate floor effects. Emerging disease-modifying trials necessitate the precise and granular measurement of communication to determine drug efficacy. This study evaluated a new measure of communication for CDD called the Communication Inventory Disability – Observer Reported (CID-OR).

methodsCID-OR was developed using a communication framework for CDD created from qualitative data and informed through evaluation of current measures and consultation with clinical experts. Scores for items describing communicative purpose were derived from ratings of consistency and the mode of delivery. An online survey was administered to parents of people with CDD (n = 184) recruited from the International CDKL5 Clinical Research Network. Most caregivers (96%) completed the Communication and Symbolic Behavior Scales - Developmental Profile Infant Toddler Checklist (CSBS–DP ITC). A confirmatory factor analysis was conducted. Test-retest reliability and comparison of known groups were assessed using intraclass correlation coefficients and linear regression, respectively.

resultsThe median age of people with CDD was 9.8 (1–43) years. A single factor model was evaluated. For 34 items, item loadings were satisfactory. For the scale, internal consistency and goodness-of-fit statistics were satisfactory, except for the Root Mean Square Error of Approximation statistic. The distribution of CID-OR scores was less right skewed than for CSBS-DP ITC scores although there was a high correlation between CID-OR and CSBS scores (r = 0.89). Test-retest reliability was high (ICC 0.966).

conclusionPreliminary analysis suggests that CID-OR is a reliable and valid measure of communication in CDD. This new tool has strong potential to measure responsiveness to interventions in CDD and may extend to similar developmental and epileptic encephalopathy conditions.

Indexed as

CommunicationEpileptic SyndromesSpasms, InfantileAdolescentAdultChildChild, PreschoolFemaleHumansInfantMaleParentsPsychometricsReproducibility of ResultsSurveys and QuestionnairesCDKL5 deficiency disorderCommunicationDevelopmental and epileptic encephalopathyOutcome measurePsychometric

Identifiers

PMID41364294
PMCPMC12799820

What Socratic holds

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Registered trials

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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 Socratic graph.