Evidence map›Paper›PMID 42712201›Full record

ArticleMuscle & nerve2026

Construct Validity and Reliability of the OMNI Scale in Children and Adolescents With Neuromuscular Diseases.

Juliana Cardoso, Clara Corsete Tonoli, Beatriz Parra Buzzetti, Gabriela Barroso Davoli, Ana Claudia Mattiello-Sverzut

Abstract readValidation Study
In one paragraph

Article in Muscle & nerve, 2026. 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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Juliana CardosoDepartment of Health Science, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0001-5870-261X
Clara Corsete TonoliDepartment of Health Science, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0009-0005-2883-4677
Beatriz Parra BuzzettiDepartment of Health Science, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo, Brazil.
Gabriela Barroso DavoliDepartment of Health Science, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo, Brazil.
Ana Claudia Mattiello-SverzutDepartment of Health Science, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-4181-0718

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 88887.837023/2023-00Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/17596-4Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/04369-5Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/19878-2Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/09029-3
6 · The paper itself

Abstract

INTRODUCTION/

aimsChildren and adolescents with neuromuscular diseases often demonstrate muscle weakness and mobility limitations, which may increase perceived exertion during functional tasks. The OMNI scale was developed to assess perceived exertion in pediatric populations; however, its measurement properties in neuromuscular conditions remain unclear. This study aimed to examine the construct validity of the OMNI scale, using the Borg scale as a reference, and its inter-rater reliability during the 6-minute walk test (6MWT) in children and adolescents with Charcot-Marie-Tooth disease (CMT) and myopathies.

methodsConstruct validity was analyzed in 39 participants, and inter-rater reliability in 21 participants aged 4-18 years. Perceived exertion was assessed before, during, and after the 6MWT using the OMNI and Borg scales. Linear mixed-effects models examined construct validity. The intraclass correlation coefficient (ICC) and standard error of measurement (SEM) assessed reliability.

resultsA significant association was observed between Borg and OMNI scores (β = 0.82, p < 0.001). OMNI scores increased throughout the 6MWT, indicating changes in perceived exertion. Inter-rater reliability was moderate at the second minute (ICC = 0.67; 95% CI 0.34-0.85) and high at the end of the 6MWT (ICC = 0.75; 95% CI 0.48-0.89). The SEM was 1.74 points at the second minute and 1.32 points at the end of the 6MWT. DISCUSSION: The OMNI scale demonstrated good construct validity and acceptable inter-rater reliability, with low measurement error, supporting its clinical applicability. This suggests that the OMNI scale is a practical and reliable tool for monitoring perceived exertion in children and adolescents with neuromuscular diseases.

Indexed as

Charcot-Marie-Tooth DiseaseNeuromuscular DiseasesPhysical ExertionAdolescentChildChild, PreschoolFemaleHumansMaleReproducibility of ResultsWalk TestCharcot–Marie–Tooth diseaseDuchenne muscular dystrophymyopathyphysical exertionrehabilitation

Identifiers

PMID42712201
PMCPMC13644902

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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 OpenQuestion graph.