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Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity

Introduction: Spasticity is a typical motor disorder in patients affected by stroke. Typically post-stroke rehabilitation consists of repetition of mobilization exercises on impaired limbs, aimed to reduce muscle hypertonia and mitigate spastic reflexes. It is currently strongly debated if the treat...

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Autores principales: Crea, Simona, Cempini, Marco, Mazzoleni, Stefano, Carrozza, Maria Chiara, Posteraro, Federico, Vitiello, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427118/
https://www.ncbi.nlm.nih.gov/pubmed/28553200
http://dx.doi.org/10.3389/fnins.2017.00261
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author Crea, Simona
Cempini, Marco
Mazzoleni, Stefano
Carrozza, Maria Chiara
Posteraro, Federico
Vitiello, Nicola
author_facet Crea, Simona
Cempini, Marco
Mazzoleni, Stefano
Carrozza, Maria Chiara
Posteraro, Federico
Vitiello, Nicola
author_sort Crea, Simona
collection PubMed
description Introduction: Spasticity is a typical motor disorder in patients affected by stroke. Typically post-stroke rehabilitation consists of repetition of mobilization exercises on impaired limbs, aimed to reduce muscle hypertonia and mitigate spastic reflexes. It is currently strongly debated if the treatment's effectiveness improves with the timeliness of its adoption; in particular, starting intensive rehabilitation as close as possible to the stroke event may counteract the growth and postpone the onset of spasticity. In this paper we present a phase-II clinical validation of a robotic exoskeleton in treating subacute post-stroke patients. Methods: Seventeen post-stroke patients participated in 10 daily rehabilitation sessions using the NEUROExos Elbow Module exoskeleton, each one lasting 45 min: the exercises consisted of isokinetic passive mobilization of the elbow, with torque threshold to detect excessive user's resistance to the movement. We investigated the safety by reporting possible adverse events, such as mechanical, electrical or software failures of the device or injuries or pain experienced by the patient. As regards the efficacy, the Modified Ashworth Scale, was identified as primary outcome measure and the NEEM metrics describing elbow joint resistance to passive extension (i.e., maximum extension torque and zero-torque angle) as secondary outcomes. Results: During the entire duration of the treatments no failures or adverse events for the patients were reported. No statistically significant differences were found in the Modified Ashworth Scale scores, between pre-treatment and post-treatment and between post-treatment and follow-up sessions, indicating the absence of spasticity increase throughout (14 days) and after (3–4 months follow-up) the treatment. Exoskeleton metrics confirmed the absence of significant difference in between pre- and post-treatment data, whereas intra-session data highlighted significant differences in the secondary outcomes, toward a decrease of the subject's joint resistance. Conclusions: The results show that our robotic exoskeleton can be safely used for prolonged sessions in post-stroke and suggest that intensive early rehabilitation treatment may prevent the occurrence of spasticity at a later stage. Moreover, the NEEM metrics were found to be reliable compared to the Modified Ashworth Scale and sensitive to revealing intra-session changes of elbow resistance to passive extension, in agreement with clinical evidences.
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spelling pubmed-54271182017-05-26 Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity Crea, Simona Cempini, Marco Mazzoleni, Stefano Carrozza, Maria Chiara Posteraro, Federico Vitiello, Nicola Front Neurosci Neuroscience Introduction: Spasticity is a typical motor disorder in patients affected by stroke. Typically post-stroke rehabilitation consists of repetition of mobilization exercises on impaired limbs, aimed to reduce muscle hypertonia and mitigate spastic reflexes. It is currently strongly debated if the treatment's effectiveness improves with the timeliness of its adoption; in particular, starting intensive rehabilitation as close as possible to the stroke event may counteract the growth and postpone the onset of spasticity. In this paper we present a phase-II clinical validation of a robotic exoskeleton in treating subacute post-stroke patients. Methods: Seventeen post-stroke patients participated in 10 daily rehabilitation sessions using the NEUROExos Elbow Module exoskeleton, each one lasting 45 min: the exercises consisted of isokinetic passive mobilization of the elbow, with torque threshold to detect excessive user's resistance to the movement. We investigated the safety by reporting possible adverse events, such as mechanical, electrical or software failures of the device or injuries or pain experienced by the patient. As regards the efficacy, the Modified Ashworth Scale, was identified as primary outcome measure and the NEEM metrics describing elbow joint resistance to passive extension (i.e., maximum extension torque and zero-torque angle) as secondary outcomes. Results: During the entire duration of the treatments no failures or adverse events for the patients were reported. No statistically significant differences were found in the Modified Ashworth Scale scores, between pre-treatment and post-treatment and between post-treatment and follow-up sessions, indicating the absence of spasticity increase throughout (14 days) and after (3–4 months follow-up) the treatment. Exoskeleton metrics confirmed the absence of significant difference in between pre- and post-treatment data, whereas intra-session data highlighted significant differences in the secondary outcomes, toward a decrease of the subject's joint resistance. Conclusions: The results show that our robotic exoskeleton can be safely used for prolonged sessions in post-stroke and suggest that intensive early rehabilitation treatment may prevent the occurrence of spasticity at a later stage. Moreover, the NEEM metrics were found to be reliable compared to the Modified Ashworth Scale and sensitive to revealing intra-session changes of elbow resistance to passive extension, in agreement with clinical evidences. Frontiers Media S.A. 2017-05-12 /pmc/articles/PMC5427118/ /pubmed/28553200 http://dx.doi.org/10.3389/fnins.2017.00261 Text en Copyright © 2017 Crea, Cempini, Mazzoleni, Carrozza, Posteraro and Vitiello. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Crea, Simona
Cempini, Marco
Mazzoleni, Stefano
Carrozza, Maria Chiara
Posteraro, Federico
Vitiello, Nicola
Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity
title Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity
title_full Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity
title_fullStr Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity
title_full_unstemmed Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity
title_short Phase-II Clinical Validation of a Powered Exoskeleton for the Treatment of Elbow Spasticity
title_sort phase-ii clinical validation of a powered exoskeleton for the treatment of elbow spasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427118/
https://www.ncbi.nlm.nih.gov/pubmed/28553200
http://dx.doi.org/10.3389/fnins.2017.00261
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