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

PLOS Digit Health. 2025 Jan 13;4(1):e0000534. doi: 10.1371/journal.pdig.0000534. eCollection 2025 Jan.

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.

Design: Prospective, multicentre, non-interventional study.

Methods: Ninety-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.

Results: The 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.

Conclusion: The 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.

Grants and funding

Digital tablets used during the study were purchased using a grant from FONDATION EOVI MCD, Paris –France (grant number: EO5-001). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.