A Pre-Registered, Open Pipeline for Early Cerebral Palsy Risk Assessment from Infant Videos

Melanie Segado1,2,3, Laura A Prosser4,3, Andrea F Duncan4,5

  • 1Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, United States.

Insights

This study developed an automated pipeline for predicting Cerebral Palsy (CP) risk using General Movements Assessment (GMA) from infant videos. The approach enables broader data sharing and model training for more accessible CP screening tools.

Area of Science:

  • Neurology
  • Developmental Pediatrics
  • Biomedical Engineering

Background:

  • Cerebral Palsy (CP) affects 1 in 500 children, impacting motor control due to abnormal brain development.
  • Early detection via General Movements Assessment (GMA) at 3-4 months is crucial for CP risk assessment.
  • Current machine learning models for GMA prediction lack generalizability and require dataset-specific tuning, hindering clinical application and data sharing.

Purpose of the Study:

  • To develop a generalizable, end-to-end machine learning pipeline for predicting GMA scores from infant videos.
  • To overcome limitations of existing models, such as dataset-specific tuning and privacy constraints, enabling multi-site data aggregation.
  • To establish groundwork for robust, globally accessible CP screening tools, particularly for low-resource settings.

Main Methods:

  • An end-to-end pipeline was created using off-the-shelf pose estimation and general-purpose feature extraction.
  • Automated machine learning (AutoML) was employed, with no dataset-specific tuning.
  • The approach was applied to a new dataset of 1063 infants from a high-risk cohort, with evaluation on a locked validation set.

Main Results:

  • The model achieved moderate predictive accuracy for clinician-assessed GMA scores.
  • Key performance metrics included an Area Under the Receiver Operating Characteristic Curve (ROC-AUC) of 0.79 and an Area Under the Precision-Recall Curve (PR-AUC) of 0.34.
  • The performance is noteworthy given the 12% positive class prevalence in the dataset.

Conclusions:

  • The developed pipeline offers a generalizable approach for GMA-based CP risk prediction.
  • Open-sourcing code and de-identified data facilitates further research and development of CP screening tools.
  • This work supports the creation of robust, accessible CP screening solutions for diverse clinical settings.

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