Automated identification of abnormal infant movements from smart phone videos

PLOS Digit Health. 2024 Feb 22;3(2):e0000432. doi: 10.1371/journal.pdig.0000432. eCollection 2024 Feb.

Abstract

Cerebral palsy (CP) is the most common cause of physical disability during childhood, occurring at a rate of 2.1 per 1000 live births. Early diagnosis is key to improving functional outcomes for children with CP. The General Movements (GMs) Assessment has high predictive validity for the detection of CP and is routinely used in high-risk infants but only 50% of infants with CP have overt risk factors when they are born. The implementation of CP screening programs represents an important endeavour, but feasibility is limited by access to trained GMs assessors. To facilitate progress towards this goal, we report a deep-learning framework for automating the GMs Assessment. We acquired 503 videos captured by parents and caregivers at home of infants aged between 12- and 18-weeks term-corrected age using a dedicated smartphone app. Using a deep learning algorithm, we automatically labelled and tracked 18 key body points in each video. We designed a custom pipeline to adjust for camera movement and infant size and trained a second machine learning algorithm to predict GMs classification from body point movement. Our automated body point labelling approach achieved human-level accuracy (mean ± SD error of 3.7 ± 5.2% of infant length) compared to gold-standard human annotation. Using body point tracking data, our prediction model achieved a cross-validated area under the curve (mean ± S.D.) of 0.80 ± 0.08 in unseen test data for predicting expert GMs classification with a sensitivity of 76% ± 15% for abnormal GMs and a negative predictive value of 94% ± 3%. This work highlights the potential for automated GMs screening programs to detect abnormal movements in infants as early as three months term-corrected age using digital technologies.

Grants and funding

This work was supported by the Murdoch Children’s Research Institute (Clinician Scientist Fellowship to EP), Rebecca L Cooper Medical Research Foundation (PG2019421 to GB), National Health and Medical Research Council Investigator Grant (1194497 to GB; 2016390 to JC), NVIDIA Corporation Hardware Grant program and The Royal Children’s Hospital Foundation, Melbourne. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.