Evidence map›Paper›PMID 41402879›Full record

ReviewResearch involvement and engagement2025

Gross motor functional classification for arthrogryposis multiplex congenita: protocol for co-development involving public with lived and professional experience.

Clarice R S Araujo, Lauren Hyer, Susan E Sienko, Cathleen Buckon, Camille Costa, Daniel Natera-de Benito, Maureen Donohoe, Kristen Donlevie, Melissa Emblin, Alicja Fafara and 3 more

Abstract readReview
In one paragraph

Review in Research involvement and engagement, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Clarice R S AraujoShriners Hospitals for Children, Montreal, Canada. clarice.araujo@shrinenet.org.ORCID http://orcid.org/0000-0002-4590-9088
Lauren HyerShriners Children's, Greenville, South Carolina, USA.ORCID http://orcid.org/0000-0003-3569-2513
Susan E SienkoShriners Children's, Portland, Oregon, USA.ORCID http://orcid.org/0000-0002-6095-6034
Cathleen BuckonShriners Children's, Portland, Oregon, USA.
Camille CostaShriners Hospitals for Children, Montreal, Canada.ORCID http://orcid.org/0009-0007-0505-3178
Daniel Natera-de BenitoNeuromuscular Unit, Department of Neurology, Hospital Sant Joan de Déu, Barcelona, Spain; Group of Applied Research in Neuromuscular Diseases, Institut de Recerca Sant Joan de Déu, Barcelona, Spain; Center for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain.ORCID http://orcid.org/0000-0001-7764-2085
Maureen DonohoeNemours Alfred I. Dupont, Delaware, Ohio, USA.ORCID http://orcid.org/0000-0001-8878-1857
Kristen DonlevieNAPA Center, Boston, Massachusetts, USA.
Melissa EmblinFamily Representative, Montreal, Canada.
Alicja FafaraInstitute of Physiotherapy, Jagiellonian University Medical College, Krakow, Poland.ORCID http://orcid.org/0000-0003-0641-846X
Jennifer C SullivanOregon Health & Science University, Portland, Oregon, USA.
Noémi Dahan-OlielShriners Hospitals for Children, Montreal, Canada.ORCID http://orcid.org/0000-0001-8567-7173
AMC Registry Team members

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildren with arthrogryposis multiplex congenita (AMC), a group of over 400 conditions characterized by congenital joint contractures, present with a wide range of gross motor functioning and mobility due to the heterogeneity of underlying diagnoses and physical involvement. Existing classification systems for AMC focus primarily on etiology and anatomical distribution but do not describe differences in gross motor functioning. In contrast, condition-specific functional classification systems have improved communication, treatment planning, and research by stratifying individuals based on functional ability. To date, no such classification system exists for AMC. This study aims to co-develop and evaluate the Gross Motor Functional Classification for Arthrogryposis Multiplex Congenita (GMFC-AMC), a condition-specific tool to support clinical and research needs.

methodsThis multi-phase study involves stakeholders with lived and professional experience in AMC from multiple countries. Phase 1 includes the initial drafting of the GMFC-AMC by an expert panel. In Phase 2, nominal group techniques are used to refine the draft. Phase 3 employs Delphi surveys to achieve international consensus on relevance, clarity, and comprehensibility. In Phase 4, the GMFC-AMC is translated and culturally adapted into French and Spanish following a structured cross-cultural adaptation process. Finally, Phase 5 evaluates reliability and construct validity across three languages. Inter-rater and test-retest reliability will be examined using video ratings of children with AMC. Construct validity will be assessed through correlations with established measures, including the Gillette Functional Assessment Questionnaire and the Pediatric Evaluation of Disability Inventory – Computer Adaptive Test. DISCUSSION: The GMFC-AMC will address a critical gap in functional classification for children and youth with AMC by providing a standardized language for describing gross motor functioning. By engaging international stakeholders throughout the development process and ensuring rigorous testing of its psychometric properties, the GMFC-AMC is expected to be a reliable, valid, and meaningful tool across diverse clinical and cultural contexts. This classification will facilitate clearer communication, improve care planning, and enable stratification for future longitudinal and interventional studies in AMC populations.

trial registrationClinical trial number not applicable.

Indexed as

Arthrogryposis multiplex congenitaChildrenDisabilityFunctional classificationGross motorMobilityYouth

Identifiers

PMID41402879
PMCPMC12884608

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.