Institut Català de la Salut
[de Gorostegui A] PhD Program in Neuroscience, Universidad Autonoma de Madrid-Cajal Institute, Madrid, Spain. Department of Anatomy, Histology & Neuroscience, School of Medicine, Universidad Autónoma de Madrid (UAM), Madrid, Spain. [Zanin M] Instituto de Física Interdisciplinar y Sistemas Complejos IFISC (CSIC-UIB), Campus UIB, Palma de Mallorca, Spain. [Martín-Gonzalo JA] Escuela Universitaria de Fisioterapia de la ONCE, Universidad Autónoma de Madrid, Madrid, Spain. [López-López J] Department of Rehabilitation, Hospital Universitario Infanta Sofía, Madrid, Spain. Fundación para la Investigación e Innovación Biomédica del Hospital Universitario Infanta Sofía y Hospital del Henares, Madrid, Spain. Departamento de Medicina, Salud y Deporte, Universidad Europea de Madrid, Villaviciosa de Odón, Madrid, Spain. [Gómez-Andrés D] Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Servei de Neurologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Kiernan D] Movement Analysis Laboratory, Central Remedial Clinic, Clontarf, Dublin, Ireland
Vall d'Hebron Barcelona Hospital Campus
2025-09-16T12:24:03Z
2025-09-16T12:24:03Z
2025-07
Cerebral palsy; Deep learning; Entropy
Parálisis cerebral; Aprendizaje profundo; Entropía
Paràlisi cerebral; Aprenentatge profund; Entropia
The use of gait analysis to differentiate among paediatric populations with neurological and developmental conditions such as idiopathic toe walking (ITW), cerebral palsy (CP), and hereditary spastic paraplegia (HSP) remains challenging due to the insufficient precision of current diagnostic approaches, leading in some cases to misdiagnosis. Existing methods often isolate the analysis of gait variables, overlooking the whole complexity of biomechanical patterns and variations in motor control strategies. While previous studies have explored the use of statistical physics principles for the analysis of impaired gait patterns, gaps remain in integrating both kinematic and kinetic information or benchmarking these approaches against Deep Learning models. This study evaluates the robustness of statistical physics metrics in differentiating between normal and abnormal gait patterns and quantifies how the data source affects model performance. The analysis was conducted using gait data sets from two research institutions in Madrid and Dublin, with a total of 81 children with ITW, 300 with CP, 20 with HSP, and 127 typically developing children as controls. From each kinematic and kinetic time series, Shannon’s entropy, permutation entropy, weighted permutation entropy, and time irreversibility metrics were derived and used with Random Forest models. The classification accuracy of these features was compared to a ResNet Deep Learning model. Further analyses explored the effects of inter-laboratory comparisons and the spatiotemporal resolution of time series on classification performance and evaluated the impact of age and walking speed with linear mixed models. The results revealed that statistical physics metrics were able to differentiate among impaired gait patterns, achieving classification scores comparable to ResNet. The effects of walking speed and age on gait predictability and temporal organisation were observed as disease-specific patterns. However, performance differences across laboratories limit the generalisation of the trained models. These findings highlight the value of statistical physics metrics in the classification of children with different toe walking conditions and point towards the need of multimetric integration to improve diagnostic accuracy and gain a more comprehensive understanding of gait disorders.
This research study was funded by Escuela Universitaria de Fisioterapia ONCE-UAM and TACTIC project—FORTALECE ISCIII grant No. FORT23/00034 and grant CNS2023-144775 funded by MICIU/AEI/10.13039/501100011033 by “European Union NextGenerationEU/PRTR”. This project also received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (Grant Agreement No. 851255). This work was partially supported by María de Maeztu project CEX2021-001164-M funded by MCIN/AEI/10.13039/501100011033 and FEDER, EU. This research study was supported by a grant for an international stay within the Universidad Autónoma de Madrid travel grants program for participation in International Research Conferences.
Article
Versió publicada
Anglès
Caminades; Infants; Paràlisi cerebral; Paràlisi espàstica; Entropia; Aprenentatge profund; DISEASES::Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Brain Damage, Chronic::Cerebral Palsy; NAMED GROUPS::Persons::Age Groups::Child; PHENOMENA AND PROCESSES::Mathematical Concepts::Algorithms::Artificial Intelligence::Machine Learning::Deep Learning; PHENOMENA AND PROCESSES::Physical Phenomena::Thermodynamics::Entropy; DISEASES::Nervous System Diseases::Nervous System Malformations::Hereditary Sensory and Motor Neuropathy::Spastic Paraplegia, Hereditary; PHENOMENA AND PROCESSES::Musculoskeletal and Neural Physiological Phenomena::Musculoskeletal Physiological Phenomena::Movement::Locomotion::Walking::Gait; ENFERMEDADES::enfermedades del sistema nervioso::enfermedades del sistema nervioso central::enfermedades cerebrales::daño encefálico crónico::parálisis cerebral; DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::niño; FENÓMENOS Y PROCESOS::conceptos matemáticos::algoritmos::inteligencia artificial::aprendizaje automático::aprendizaje profundo; FENÓMENOS Y PROCESOS::fenómenos físicos::termodinámica::entropía; ENFERMEDADES::enfermedades del sistema nervioso::malformaciones del sistema nervioso::neuropatía sensitiva y motora hereditaria::paraplejía espástica hereditaria; FENÓMENOS Y PROCESOS::fenómenos fisiológicos nerviosos y musculoesqueléticos::fenómenos fisiológicos musculoesqueléticos::movimiento::locomoción::caminata::marcha
MDPI
Sensors;25(13)
https://doi.org/10.3390/s25134235
info:eu-repo/grantAgreement/EC/H2020/851255
Attribution 4.0 International
http://creativecommons.org/licenses/by/4.0/
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