Evidence map›Paper›PMID 41124586›Full record

ArticleDevelopmental medicine and child neurology2026

Psychometric properties of functional mobility outcome measures in children with arthrogryposis multiplex congenita.

Ahlam Zidan, Laurie Snider, Emmanouil Rampakakis, Reggie Hamdy, Frank Rauch, Noémi Dahan-Oliel

Abstract read
In one paragraph

Article in Developmental medicine and child neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ahlam ZidanFaculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.ORCID 0000-0002-5210-0009
Laurie SniderFaculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.
Emmanouil RampakakisFaculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.ORCID 0000-0002-7427-8246
Reggie HamdyFaculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.
Frank RauchFaculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.ORCID 0000-0002-6261-0360
Noémi Dahan-OlielFaculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.ORCID 0000-0001-8567-7173

Funding

American Society for Bone and Mineral ResearchCentre for Interdisciplinary Research in RehabilitationFaculty of Medicine, McGill UniversityFonds de Recherche du Québec - Santé 267793Fonds de Recherche du Québec - Santé 329833Islamic Developmental Bank (IsDB)Shriners Hospitals for Children 79137Shriners Hospitals for Children 79150
6 · The paper itself

Abstract

aimTo establish the construct validity, agreement, and minimal important difference (MID) of widely used mobility measures in arthrogryposis multiplex congenita (AMC).

methodParticipants (n = 248, 126 males, mean age 10 years 10 months, standard deviation 3 years 11 months) with AMC were assessed using the Functional Mobility Scale (FMS), Gillette Functional Assessment Questionnaire (FAQ), Functional Independence Measure for Children (WeeFIM), and Patient-Reported Outcomes Measurement Information System (PROMIS). Convergent and discriminant validity were evaluated using Spearman's rank correlations, while known-groups validity was examined using analysis of variance. Cohen's kappa and distribution-based methods were used to estimate agreement and MIDs respectively.

resultsRobust convergent (ρ = 0.66-0.82, 95% confidence interval [CI] 0.54-0.86) and discriminant (ρ = 0.06-0.31, 95% CI -0.11 to 0.43) validity were found for all four mobility measures. Known-groups validity was supported by significant mean differences across AMC subtypes (amyoplasia, distal arthrogryposis, central nervous system/syndromic; p < 0.001). The measures also showed weak to good agreement in classifying mobility. A difference of one and two levels on the FMS and FAQ respectively, was found to be minimally important. For the PROMIS and WeeFIM, estimated MID values were 3.19 to 4.34 and 14.24 respectively.

interpretationThe robust construct validity, agreement, and MIDs provide clinicians and researchers with evidence-based benchmarks for assessing mobility in children with AMC.

Indexed as

ArthrogryposisMobility LimitationOutcome Assessment, Health CarePatient Reported Outcome MeasuresPsychometricsAdolescentChildChild, PreschoolDisability EvaluationFemaleHumansMaleReproducibility of Results

Identifiers

PMID41124586
PMCPMC13160398

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