Gait Characterization in Duchenne Muscular Dystrophy (DMD) Using a Single-Sensor Accelerometer: Classical Machine Learning and Deep Learning Approaches
Albara Ah Ramli, Xin Liu, Kelly Berndt, Erica Goude, Jiahui Hou, Lynea, B. Kaethler, Rex Liu, Amanda Lopez, Alina Nicorici, Corey Owens, David, Rodriguez, Jane Wang, Huanle Zhang, Daniel Aranki, Craig M. McDonald, Erik K., Henricson

TL;DR
This study uses smartphone accelerometers and machine learning to quantify and differentiate gait patterns in children with Duchenne Muscular Dystrophy from typically developing peers across various walking speeds.
Contribution
It introduces a novel approach combining consumer-grade accelerometers and ML to detect DMD gait features outside laboratory settings.
Findings
Reduced step length in DMD children
Greater mediolateral power in DMD gait
ML achieved up to 100% accuracy in classification
Abstract
Differences in gait patterns of children with Duchenne muscular dystrophy (DMD) and typically-developing (TD) peers are visible to the eye, but quantifications of those differences outside of the gait laboratory have been elusive. In this work, we measured vertical, mediolateral, and anteroposterior acceleration using a waist-worn iPhone accelerometer during ambulation across a typical range of velocities. Fifteen TD and fifteen DMD children from 3-16 years of age underwent eight walking/running activities, including five 25 meters walk/run speed-calibration tests at a slow walk to running speeds (SC-L1 to SC-L5), a 6-minute walk test (6MWT), a 100 meters fast-walk/jog/run (100MRW), and a free walk (FW). For clinical anchoring purposes, participants completed a Northstar Ambulatory Assessment (NSAA). We extracted temporospatial gait clinical features (CFs) and applied multiple machine…
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Taxonomy
TopicsMuscle Physiology and Disorders · Prosthetics and Rehabilitation Robotics · Muscle activation and electromyography studies
