Abstract

Background: Objective gait assessment is key for the follow-up of patients with progressive multiple sclerosis (pMS). Inertial measurement units (IMUs) provide reliable and yet easy quantitative gait assessment in routine clinical settings. However, to the best of our knowledge, no automated step-detection algorithm performs well in detecting severely altered pMS gait.Method: This article elaborates on a step-detection method based on personalized templates tested against a gold standard. Twenty-two individuals with pMS and 10 young healthy subjects (HSs) were instructed to walk on an electronic walkway wearing synchronized IMUs. Templates were derived from the IMU signals by using Initial and Final Contact times given by the walkway. These were used to detect steps from other gait trials of the same individual (intra-individual template-based detection, IITD) or another participant from the same group (pMS or HS) (intra-group template-based detection, IGTD). All participants were seen twice with a 6-month interval, with two measurements performed at each visit. Performance and accuracy metrics were computed, along with a similarity index (SId), which was computed as the mean distance between detected steps and their respective closest template.Results: For HS participants, both the IITD and the IGTD algorithms had precision and recall of 1.00 for detecting steps. For pMS participants, precision and recall ranged from 0.94 to 1.00 for IITD and 0.85 to 0.95 for IGTD depending on the level of disability. The SId was correlated with performance and the accuracy of the result. An SId threshold of 0.957 (IITD) and 0.963 (IGTD) could rule out decreased performance (F-measure ≤ 0.95), with negative predictive values of 0.99 and 0.96 with the IITD and IGTD algorithms. Also, the SId computed with the IITD and IGTD algorithms could distinguish individuals showing changes at 6-month follow-up.Conclusion: This personalized step-detection method has high performance for detecting steps in pMS individuals with severely altered gait. The algorithm can be self-evaluating with the SI, which gives a measure of the confidence the clinician can have in the detection. What is more, the SId can be used as a biomarker of change in disease severity occurring between the two measurement times.

Highlights

  • Multiple sclerosis (MS) is a demyelinating disease of the central nervous system with varying clinical presentation and progression

  • We derived a measure of similarity between templates and detected steps, the similarity index (SId) [28], and we show that this measure is a marker of the performance and accuracy of the algorithm, providing the clinician with an indicator of confidence in detecting steps of individuals with progressive multiple sclerosis (pMS)

  • We present two main configurations: intra-individual template-based detection (IITD) where the reference and detection trials belong to the same subject and intra-group template-based detection (IGTD) where they belong to different subjects

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Summary

Introduction

Multiple sclerosis (MS) is a demyelinating disease of the central nervous system with varying clinical presentation and progression. Objective gait assessment is needed in both routine clinical care and clinical research trials to improve gait and balance follow-up in people with MS. Stopwatch-timed tests and clinical scales are used in routine daily practice to assess gait impairments. They are prone to practice effects [2] and variability [3, 4]. We need objective and easy-to-perform gait assessment tools to detect such alterations. Objective gait assessment is key for the follow-up of patients with progressive multiple sclerosis (pMS). Inertial measurement units (IMUs) provide reliable and yet easy quantitative gait assessment in routine clinical settings. To the best of our knowledge, no automated step-detection algorithm performs well in detecting severely altered pMS gait

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