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Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates

BACKGROUND: Brain-machine interfaces (BMI) have recently been integrated within motor rehabilitation therapies by actively involving the central nervous system (CNS) within the exercises. For instance, the online decoding of intention of motion of a limb from pre-movement EEG correlates is being use...

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Autores principales: López-Larraz, Eduardo, Montesano, Luis, Gil-Agudo, Ángel, Minguez, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247645/
https://www.ncbi.nlm.nih.gov/pubmed/25398273
http://dx.doi.org/10.1186/1743-0003-11-153
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author López-Larraz, Eduardo
Montesano, Luis
Gil-Agudo, Ángel
Minguez, Javier
author_facet López-Larraz, Eduardo
Montesano, Luis
Gil-Agudo, Ángel
Minguez, Javier
author_sort López-Larraz, Eduardo
collection PubMed
description BACKGROUND: Brain-machine interfaces (BMI) have recently been integrated within motor rehabilitation therapies by actively involving the central nervous system (CNS) within the exercises. For instance, the online decoding of intention of motion of a limb from pre-movement EEG correlates is being used to convert passive rehabilitation strategies into active ones mediated by robotics. As early stages of upper limb motor rehabilitation usually focus on analytic single-joint mobilizations, this paper investigates the feasibility of building BMI decoders for these specific types of movements. METHODS: Two different experiments were performed within this study. For the first one, six healthy subjects performed seven self-initiated upper-limb analytic movements, involving from proximal to distal articulations. For the second experiment, three spinal cord injury patients performed two of the previously studied movements with their healthy elbow and paralyzed wrist. In both cases EEG neural correlates such as the event-related desynchronization (ERD) and movement related cortical potentials (MRCP) were analyzed, as well as the accuracies of continuous decoders built using the pre-movement features of these correlates (i.e., the intention of motion was decoded before movement onset). RESULTS: The studied movements could be decoded in both healthy subjects and patients. For healthy subjects there were significant differences in the EEG correlates and decoding accuracies, dependent on the moving joint. Percentages of correctly anticipated trials ranged from 75% to 40% (with chance level being around 20%), with better performances for proximal than for distal movements. For the movements studied for the SCI patients the accuracies were similar to the ones of the healthy subjects. CONCLUSIONS: This paper shows how it is possible to build continuous decoders to detect movement intention from EEG correlates for seven different upper-limb analytic movements. Furthermore we report differences in accuracies among movements, which might have an impact on the design of the rehabilitation technologies that will integrate this new type of information. The applicability of the decoders was shown in a clinical population, with similar performances between healthy subjects and patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1743-0003-11-153) contains supplementary material, which is available to authorized users.
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spelling pubmed-42476452014-11-30 Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates López-Larraz, Eduardo Montesano, Luis Gil-Agudo, Ángel Minguez, Javier J Neuroeng Rehabil Research BACKGROUND: Brain-machine interfaces (BMI) have recently been integrated within motor rehabilitation therapies by actively involving the central nervous system (CNS) within the exercises. For instance, the online decoding of intention of motion of a limb from pre-movement EEG correlates is being used to convert passive rehabilitation strategies into active ones mediated by robotics. As early stages of upper limb motor rehabilitation usually focus on analytic single-joint mobilizations, this paper investigates the feasibility of building BMI decoders for these specific types of movements. METHODS: Two different experiments were performed within this study. For the first one, six healthy subjects performed seven self-initiated upper-limb analytic movements, involving from proximal to distal articulations. For the second experiment, three spinal cord injury patients performed two of the previously studied movements with their healthy elbow and paralyzed wrist. In both cases EEG neural correlates such as the event-related desynchronization (ERD) and movement related cortical potentials (MRCP) were analyzed, as well as the accuracies of continuous decoders built using the pre-movement features of these correlates (i.e., the intention of motion was decoded before movement onset). RESULTS: The studied movements could be decoded in both healthy subjects and patients. For healthy subjects there were significant differences in the EEG correlates and decoding accuracies, dependent on the moving joint. Percentages of correctly anticipated trials ranged from 75% to 40% (with chance level being around 20%), with better performances for proximal than for distal movements. For the movements studied for the SCI patients the accuracies were similar to the ones of the healthy subjects. CONCLUSIONS: This paper shows how it is possible to build continuous decoders to detect movement intention from EEG correlates for seven different upper-limb analytic movements. Furthermore we report differences in accuracies among movements, which might have an impact on the design of the rehabilitation technologies that will integrate this new type of information. The applicability of the decoders was shown in a clinical population, with similar performances between healthy subjects and patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1743-0003-11-153) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-15 /pmc/articles/PMC4247645/ /pubmed/25398273 http://dx.doi.org/10.1186/1743-0003-11-153 Text en © López-Larraz et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
López-Larraz, Eduardo
Montesano, Luis
Gil-Agudo, Ángel
Minguez, Javier
Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates
title Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates
title_full Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates
title_fullStr Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates
title_full_unstemmed Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates
title_short Continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement EEG correlates
title_sort continuous decoding of movement intention of upper limb self-initiated analytic movements from pre-movement eeg correlates
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247645/
https://www.ncbi.nlm.nih.gov/pubmed/25398273
http://dx.doi.org/10.1186/1743-0003-11-153
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