Evidence map›Paper›PMID 41752831›Full record

ArticleLife (Basel, Switzerland)2026

Selective Motor Entropy Modulation and Targeted Augmentation for the Identification of Parkinsonian Gait Patterns Using Multimodal Gait Analysis.

Yacine Benyoucef, Jouhayna Harmouch, Borhan Asadi, Islem Melliti, Antonio Del Mastro, Pablo Herrero, Alberto Carcasona-Otal, Diego Lapuente-Hernández

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Article in Life (Basel, Switzerland), 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yacine BenyoucefSpacemedex, 930 Route des Dolines, 06560 Valbonne, France.
Jouhayna HarmouchSpacemedex, 930 Route des Dolines, 06560 Valbonne, France.
Borhan AsadiDepartment of Physiatry and Nursing, Faculty of Health Sciences, University of Zaragoza, 50009 Zaragoza, Spain.ORCID 0000-0001-7505-7958
Islem MellitiNational Institute of Technology and Applied Sciences, Centre Urbain Nord BP 676, Tunis 1080, Tunisia.
Antonio Del MastroAldebran/Mars Planet Technologies, Via Dalmine 10/A, 24035 Curno, BG, Italy.
Pablo HerreroDepartment of Physiatry and Nursing, Faculty of Health Sciences, University of Zaragoza, 50009 Zaragoza, Spain.ORCID 0000-0002-9201-0120
Alberto Carcasona-OtaliHealthy Research Group, IIS Aragon, 50009 Zaragoza, Spain.ORCID 0009-0003-8000-7084
Diego Lapuente-HernándezDepartment of Physiatry and Nursing, Faculty of Health Sciences, University of Zaragoza, 50009 Zaragoza, Spain.ORCID 0000-0002-6506-6081

Funding

EDIH 101083776
6 · The paper itself

Abstract

BACKGROUND/

objectivesParkinsonian gait is characterized by impaired motor adaptability, altered temporal organization, and reduced movement variability. While data augmentation is commonly used to mitigate class imbalance in gait-based machine learning models, conventional strategies often ignore physiological differences between healthy and pathological movements, potentially distorting meaningful motor dynamics. This study explores whether preserving healthy motor variability while selectively augmenting pathological gait signals can improve the robustness and physiological coherence of gait pattern classification models.

methodsEight patients with Parkinsonian gait patterns and forty-eight healthy participants performed walking tasks on the Motigravity platform under hypogravity conditions. Full-body kinematic data were acquired using wearable inertial sensors. A selective augmentation strategy based on smooth time-warping was applied exclusively to pathological gait segments (×5, σ = 0.2), while healthy gait signals were left unaltered to preserve natural motor variability. Model performance was evaluated using a hybrid convolutional neural network-long short-term memory (CNN-LSTM) architecture across multiple augmentation configurations.

resultsSelective augmentation of pathological gait signals achieved the highest classification performance (94.1% accuracy, AUC = 0.97), with balanced sensitivity (93.8%) and specificity (94.3%). Performance decreased when augmentation exceeded an optimal range of variability, suggesting that beneficial augmentation is constrained by physiologically plausible temporal dynamics.

conclusionsThese findings demonstrate that physiology-informed, selective data augmentation can improve gait pattern classification under constrained data conditions. Rather than supporting disease-specific diagnosis, this proof-of-concept study highlights the importance of respecting intrinsic differences in motor variability when designing augmentation strategies for clinical gait analysis. Future studies incorporating disease-control cohorts and subject-independent validation are required to assess specificity and clinical generalizability.

Indexed as

gait analysismotor entropymotor variabilityParkinsonian gaitselective data augmentationtime-series classificationwearable sensors

Identifiers

PMID41752831
PMCPMC12941575

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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.