On Gait Consistency Quantification Through ARX Residual Modeling and Kernel Two-Sample Testing

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Abstract

Objective: The quantification of the way an individual walks is key to the understanding of diseases affecting the neuromuscular system. More specifically, to improve diagnostics and treatment plans, there is a continuous interest in quantifying gait consistency, allowing clinicians to distinguish natural variability of the gait patterns from disease progression or treatment effects. To this end, the current article presents a novel objective method for assessing the consistency of an individual's gait, consisting of two major components. Methods: Firstly, inertial sensor accelerometer data from both shanks and the lower back is used to fit an AutoRegressive with eXogenous input model. The model residuals are then used as a key feature for gait consistency monitoring. Secondly, the non-parametric maximum mean discrepancy hypothesis test is introduced to measure differences in the distributions of the residuals as a measure of gait consistency. As a paradigmatic case, gait consistency was evaluated both in a single walking test and between tests at different time points in healthy individuals and those affected by multiple sclerosis (MS). Results: It was found that MS patients experienced difficulties maintaining a consistent gait, even when the retest was performed one-hour apart and all external factors were controlled. When the retest was performed one-week apart, both healthy and MS individuals displayed inconsistent gait patterns. Conclusion: Gait consistency has been successfully quantified for both healthy and MS individuals. Significance: This newly proposed approach revealed the detrimental effects of varying assessment conditions on gait pattern consistency, indicating potential masking effects at follow-up assessments.

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APA

Stihi, A., Rogers, T. J., Mazza, C., & Cross, E. J. (2024). On Gait Consistency Quantification Through ARX Residual Modeling and Kernel Two-Sample Testing. IEEE Transactions on Biomedical Engineering, 71(3), 720–731. https://doi.org/10.1109/TBME.2023.3316474

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