Auto-Gait: Automatic Ataxia Risk Assessment with Computer Vision on Gait
Task Videos
- URL: http://arxiv.org/abs/2203.08215v1
- Date: Tue, 15 Mar 2022 19:28:10 GMT
- Title: Auto-Gait: Automatic Ataxia Risk Assessment with Computer Vision on Gait
Task Videos
- Abstract summary: We collected 155 videos from 89 participants, 24 controls and 65 diagnosed with (or are pre-manifest) spinocerebellar ataxias (SCAs)
We developed a method to separate the participants from their surroundings and constructed several features to capture gait characteristics like step width, step length, swing, stability, speed, etc.
Our risk-prediction model achieves 83.06% accuracy and an 80.23% F1 score. Similarly, our severity-assessment model achieves a mean absolute error (MAE) score of 0.6225 and a Pearson's correlation coefficient score of 0.7268.
- Score: 3.2268662749172097
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: In this paper, we investigated whether we can 1) detect participants with
ataxia-specific gait characteristics (risk-prediction), and 2) assess severity
of ataxia from gait (severity-assessment). We collected 155 videos from 89
participants, 24 controls and 65 diagnosed with (or are pre-manifest)
spinocerebellar ataxias (SCAs), performing the gait task of the Scale for the
Assessment and Rating of Ataxia (SARA) from 11 medical sites located in 8
different states in the United States. We developed a method to separate the
participants from their surroundings and constructed several features to
capture gait characteristics like step width, step length, swing, stability,
speed, etc. Our risk-prediction model achieves 83.06% accuracy and an 80.23% F1
score. Similarly, our severity-assessment model achieves a mean absolute error
(MAE) score of 0.6225 and a Pearson's correlation coefficient score of 0.7268.
Our models still performed competitively when evaluated on data from sites not
used during training. Furthermore, through feature importance analysis, we
found that our models associate wider steps, decreased walking speed, and
increased instability with greater ataxia severity, which is consistent with
previously established clinical knowledge. Our models create possibilities for
remote ataxia assessment in non-clinical settings in the future, which could
significantly improve accessibility of ataxia care. Furthermore, our underlying
dataset was assembled from a geographically diverse cohort, highlighting its
potential to further increase equity. The code used in this study is open to
the public, and the anonymized body pose landmark dataset could be released
upon approval from our Institutional Review Board (IRB).
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