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Fatigue-induced changes of impedance and performance in target tracking

Kinematic variability is caused, in part, by force fluctuations. It has been shown empirically and numerically that the effects of force fluctuations on kinematics can be suppressed by increasing joint impedance. Given that force variability increases with muscular fatigue, we hypothesized that join...

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Detalles Bibliográficos
Autores principales: Selen, L. P. J., Beek, P. J., van Dieën, J. H.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1914220/
https://www.ncbi.nlm.nih.gov/pubmed/17342476
http://dx.doi.org/10.1007/s00221-007-0909-0
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author Selen, L. P. J.
Beek, P. J.
van Dieën, J. H.
author_facet Selen, L. P. J.
Beek, P. J.
van Dieën, J. H.
author_sort Selen, L. P. J.
collection PubMed
description Kinematic variability is caused, in part, by force fluctuations. It has been shown empirically and numerically that the effects of force fluctuations on kinematics can be suppressed by increasing joint impedance. Given that force variability increases with muscular fatigue, we hypothesized that joint impedance would increase with fatigue to retain a prescribed accuracy level. To test this hypothesis, subjects tracked a target by elbow flexion and extension both with fatigued and unfatigued elbow flexor and extensor muscles. Joint impedance was estimated from controlled perturbations to the elbow. Contrary to the hypothesis, elbow impedance decreased, whereas performance, expressed as the time-on-target, was unaffected by fatigue. Further analysis of the data revealed that subjects changed their control strategy with increasing fatigue. Although their overall kinematic variability increased, task performance was retained by staying closer to the center of the target when fatigued. In conclusion, the present study reveals a limitation of impedance modulation in the control of movement variability.
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spelling pubmed-19142202007-07-12 Fatigue-induced changes of impedance and performance in target tracking Selen, L. P. J. Beek, P. J. van Dieën, J. H. Exp Brain Res Research Article Kinematic variability is caused, in part, by force fluctuations. It has been shown empirically and numerically that the effects of force fluctuations on kinematics can be suppressed by increasing joint impedance. Given that force variability increases with muscular fatigue, we hypothesized that joint impedance would increase with fatigue to retain a prescribed accuracy level. To test this hypothesis, subjects tracked a target by elbow flexion and extension both with fatigued and unfatigued elbow flexor and extensor muscles. Joint impedance was estimated from controlled perturbations to the elbow. Contrary to the hypothesis, elbow impedance decreased, whereas performance, expressed as the time-on-target, was unaffected by fatigue. Further analysis of the data revealed that subjects changed their control strategy with increasing fatigue. Although their overall kinematic variability increased, task performance was retained by staying closer to the center of the target when fatigued. In conclusion, the present study reveals a limitation of impedance modulation in the control of movement variability. Springer-Verlag 2007-03-07 2007-07 /pmc/articles/PMC1914220/ /pubmed/17342476 http://dx.doi.org/10.1007/s00221-007-0909-0 Text en © Springer-Verlag 2007
spellingShingle Research Article
Selen, L. P. J.
Beek, P. J.
van Dieën, J. H.
Fatigue-induced changes of impedance and performance in target tracking
title Fatigue-induced changes of impedance and performance in target tracking
title_full Fatigue-induced changes of impedance and performance in target tracking
title_fullStr Fatigue-induced changes of impedance and performance in target tracking
title_full_unstemmed Fatigue-induced changes of impedance and performance in target tracking
title_short Fatigue-induced changes of impedance and performance in target tracking
title_sort fatigue-induced changes of impedance and performance in target tracking
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1914220/
https://www.ncbi.nlm.nih.gov/pubmed/17342476
http://dx.doi.org/10.1007/s00221-007-0909-0
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