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Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial

Detecting neuroplastic changes during locomotor neurorehabilitation is crucial for independent primal motor behaviours. However, long-term locomotor training-related neuroplasticity remains unexplored. We compared the effects of end-effector robot-assisted gait training (E-RAGT) and bodyweight-suppo...

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Autores principales: Kim, Hayeon, Park, Gyulee, Shin, Joon-Ho, You, Joshua H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385173/
https://www.ncbi.nlm.nih.gov/pubmed/32719420
http://dx.doi.org/10.1038/s41598-020-69367-3
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author Kim, Hayeon
Park, Gyulee
Shin, Joon-Ho
You, Joshua H.
author_facet Kim, Hayeon
Park, Gyulee
Shin, Joon-Ho
You, Joshua H.
author_sort Kim, Hayeon
collection PubMed
description Detecting neuroplastic changes during locomotor neurorehabilitation is crucial for independent primal motor behaviours. However, long-term locomotor training-related neuroplasticity remains unexplored. We compared the effects of end-effector robot-assisted gait training (E-RAGT) and bodyweight-supported treadmill training (BWST) on cortical activation in individuals with hemiparetic stroke. Twenty-three men and five women aged 53.2 ± 11.2 years were recruited and randomly assigned to participate in E-RAGT (n = 14) or BWST (n = 14) for 30 min/day, 5 days/week, for 4 weeks. Cortical activity, lower limb motor function, and gait speed were evaluated before and after training. Activation of the primary sensorimotor cortex, supplementary motor area, and premotor cortex in the affected hemisphere significantly increased only in the E-RAGT group, although there were no significant between-group differences. Clinical outcomes, including the Fugl-Meyer assessment (FMA), timed up and go test, and 10-m walk test scores, improved after training in both groups, with significantly better FMA scores in the E-RAGT group than in the BWST group. These findings suggest that E-RAGT effectively improves neuroplastic outcomes in hemiparetic stroke, although its superiority over conventional training remains unclear. This may have clinical implications and provides insight for clinicians interested in locomotor neurorehabilitation after hemiparetic stroke. Trial Registration: ClinicalTrials.gov Identifier NCT04054739 (12/08/2019).
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spelling pubmed-73851732020-07-28 Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial Kim, Hayeon Park, Gyulee Shin, Joon-Ho You, Joshua H. Sci Rep Article Detecting neuroplastic changes during locomotor neurorehabilitation is crucial for independent primal motor behaviours. However, long-term locomotor training-related neuroplasticity remains unexplored. We compared the effects of end-effector robot-assisted gait training (E-RAGT) and bodyweight-supported treadmill training (BWST) on cortical activation in individuals with hemiparetic stroke. Twenty-three men and five women aged 53.2 ± 11.2 years were recruited and randomly assigned to participate in E-RAGT (n = 14) or BWST (n = 14) for 30 min/day, 5 days/week, for 4 weeks. Cortical activity, lower limb motor function, and gait speed were evaluated before and after training. Activation of the primary sensorimotor cortex, supplementary motor area, and premotor cortex in the affected hemisphere significantly increased only in the E-RAGT group, although there were no significant between-group differences. Clinical outcomes, including the Fugl-Meyer assessment (FMA), timed up and go test, and 10-m walk test scores, improved after training in both groups, with significantly better FMA scores in the E-RAGT group than in the BWST group. These findings suggest that E-RAGT effectively improves neuroplastic outcomes in hemiparetic stroke, although its superiority over conventional training remains unclear. This may have clinical implications and provides insight for clinicians interested in locomotor neurorehabilitation after hemiparetic stroke. Trial Registration: ClinicalTrials.gov Identifier NCT04054739 (12/08/2019). Nature Publishing Group UK 2020-07-27 /pmc/articles/PMC7385173/ /pubmed/32719420 http://dx.doi.org/10.1038/s41598-020-69367-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Hayeon
Park, Gyulee
Shin, Joon-Ho
You, Joshua H.
Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial
title Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial
title_full Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial
title_fullStr Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial
title_full_unstemmed Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial
title_short Neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial
title_sort neuroplastic effects of end-effector robotic gait training for hemiparetic stroke: a randomised controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385173/
https://www.ncbi.nlm.nih.gov/pubmed/32719420
http://dx.doi.org/10.1038/s41598-020-69367-3
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