The effects of electromyography-assisted modelling in estimating musculotendon forces during gait in children with cerebral palsy

Journal Article (2019)
Authors

Kirsten Veerkamp (Gold Coast Centre for Orthopaedic Research, Vrije Universiteit Amsterdam)

Wouter Schallig (Universiteit van Amsterdam, Vrije Universiteit Amsterdam)

J. Harlaar (TU Delft - Biomechatronics & Human-Machine Control, Vrije Universiteit Amsterdam)

Claudio Pizzolato (Gold Coast Centre for Orthopaedic Research, Griffith University)

C. P. Carty (Children’s Health Queensland Hospital and Health Service, Gold Coast Centre for Orthopaedic Research)

David G. Lloyd (Griffith University)

M.M. van der Krogt (Vrije Universiteit Amsterdam)

Research Group
Biomechatronics & Human-Machine Control
Copyright
© 2019 Kirsten Veerkamp, Wouter Schallig, J. Harlaar, Claudio Pizzolato, Christopher P. Carty, David G. Lloyd, Marjolein M. van der Krogt
To reference this document use:
https://doi.org/10.1016/j.jbiomech.2019.05.026
More Info
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Publication Year
2019
Language
English
Copyright
© 2019 Kirsten Veerkamp, Wouter Schallig, J. Harlaar, Claudio Pizzolato, Christopher P. Carty, David G. Lloyd, Marjolein M. van der Krogt
Research Group
Biomechatronics & Human-Machine Control
Volume number
92
Pages (from-to)
45-53
DOI:
https://doi.org/10.1016/j.jbiomech.2019.05.026
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Abstract

Neuro-musculoskeletal modelling can provide insight into the aberrant muscle function during walking in those suffering cerebral palsy (CP). However, such modelling employs optimization to estimate muscle activation that may not account for disturbed motor control and muscle weakness in CP. This study evaluated different forms of neuro-musculoskeletal model personalization and optimization to estimate musculotendon forces during gait of nine children with CP (GMFCS I-II)and nine typically developing (TD)children. Data collection included 3D-kinematics, ground reaction forces, and electromyography (EMG)of eight lower limb muscles. Four different optimization methods estimated muscle activation and musculotendon forces of a scaled-generic musculoskeletal model for each child walking, i.e. (i)static optimization that minimized summed-excitation squared; (ii)static optimization with maximum isometric muscle forces scaled to body mass; (iii)an EMG-assisted approach using optimization to minimize summed-excitation squared while reducing tracking errors of experimental EMG-linear envelopes and joint moments; and (iv)EMG-assisted with musculotendon model parameters first personalized by calibration. Both static optimization approaches showed a relatively low model performance compared to EMG envelopes. EMG-assisted approaches performed much better, especially in CP, with only a minor mismatch in joint moments. Calibration did not affect model performance significantly, however it did affect musculotendon forces, especially in CP. A model more consistent with experimental measures is more likely to yield more physiologically representative results. Therefore, this study highlights the importance of calibrated EMG-assisted modelling when estimating musculotendon forces in TD children and even more so in children with CP.

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