Evidence map›Paper›PMID 39804823›Full record

ArticlePLOS digital health2025

Use of assistive technology to assess distal motor function in subjects with neuromuscular disease.

Dominique Vincent-Genod, Sylvain Roche, Aurélie Barrière, Capucine de Lattre, Marie Tinat, Eelke Venema, Emmeline Lagrange, Adriana Gomes Lisboa de Souza, Guillaume Thomann, Justine Coton and 4 more

Abstract read
In one paragraph

Article in PLOS digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

14 authors.

Dominique Vincent-GenodCentre Référent Maladies Rares Neuromusculaires, Service de Médecine Physique et de Réadaptation Pédiatrique des Hospices Civils de Lyon - Hôpital Femme Mère Enfant, Bron, France.ORCID https://orcid.org/0000-0001-8564-7644
Sylvain RocheService de Biostatistique-Bioinformatique, Pôle Santé Publique des Hospices Civils de Lyon, Lyon, France.
Aurélie BarrièreCentre Référent Maladies Rares Neuromusculaires des Hospices Civils de Lyon, Hôpital de la Croix Rousse, Lyon, France.
Capucine de LattreCentre Référent Maladies Rares Neuromusculaires des Hospices Civils de Lyon, Hôpital de la Croix Rousse, Lyon, France.
Marie TinatCentre Référent Maladies Rares Neuromusculaires, Service de Médecine Physique et de Réadaptation Pédiatrique des Hospices Civils de Lyon - Hôpital Femme Mère Enfant, Bron, France.
Eelke VenemaConsultations Maladies Rares Neuromusculaires du CHU Michallon, Grenoble, France.
Emmeline LagrangeConsultations Maladies Rares Neuromusculaires du CHU Michallon, Grenoble, France.
Adriana Gomes Lisboa de SouzaUniversité. Grenoble Alpes, CNRS, Grenoble INP, Institute of Engineering Univ. Grenoble Alpes, G-SCOP, Grenoble, France.
Guillaume ThomannUniversité. Grenoble Alpes, CNRS, Grenoble INP, Institute of Engineering Univ. Grenoble Alpes, G-SCOP, Grenoble, France.ORCID https://orcid.org/0000-0001-7676-6262
Justine CotonUniversité. Grenoble Alpes, CNRS, Grenoble INP, Institute of Engineering Univ. Grenoble Alpes, G-SCOP, Grenoble, France.
Vincent GautheronUniversité Jean Monnet Saint-Etienne, Lyon 1, Université Savoie Mont-Blanc, Laboratoire Interuniversitaire de Biologie de la Motricité, Saint-Étienne, France.
Léonard FéassonUniversité Jean Monnet Saint-Etienne, Lyon 1, Université Savoie Mont-Blanc, Laboratoire Interuniversitaire de Biologie de la Motricité, Saint-Étienne, France.
Pascal RippertPôle Santé Publique, Service de Recherche et épidémiologie cliniques, Hospices Civils de Lyon, Lyon, France.ORCID https://orcid.org/0000-0003-0185-0659
Carole VuillerotCentre Référent Maladies Rares Neuromusculaires, Service de Médecine Physique et de Réadaptation Pédiatrique des Hospices Civils de Lyon - Hôpital Femme Mère Enfant, Bron, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the 32 items of the Motor Function Measure scale, 3 concern the assessment of hand function on a paper-based support. Their characteristics make it possible to envisage the use of a tablet instead of the original paper-based support for their completion. This would then make it possible to automate the score to reduce intra- and inter-individual variability. The main objective of the present study was to validate the digital completion of items 18, 19, and 22 by measuring the agreement of the scores obtained using a digital tablet with those obtained using the original paper-based support in children and adults with various neuromuscular diseases (NMD). The secondary objective is to calibrate an algorithm for the automatic items scoring.

designProspective, multicentre, non-interventional study.

methodsNinety-eight subjects aged 5 to 60 years with a confirmed NMD completed MFM items 18, 19, and 22 both on a paper support and a digital tablet.

resultsThe median age of included subjects was 16.2 years. Agreement between scores as assessed using the weighted Kappa coefficient was almost perfect for the scores of items 18 and 22 (K = 0.93, and 0.95, respectively) and substantial for item 19 (K = 0.70). In all cases of disagreement, the difference was of 1 point. The most frequent disagreement concerned item 19; mainly in the direction of a scoring of 1 point less on the tablet. An automatic analysis algorithm was tested on 82 recordings to suggest improvements.

conclusionThe switch from original paper-based support to the tablet results in minimal and acceptable differences, and maintains a valid and reproducible measure of the 3 items. The developed algorithm for automatic scoring appears feasible with the perspective to include them in a digital application that will make it easier to monitor patients.

Identifiers

PMID39804823
PMCPMC11729976

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.