Q3142425 (Q3142425): Difference between revisions
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(Created claim: summary (P836): The recovery of walking capacity is one of the main objectives of rehabilitation in people with incomplete spinal injury. Robotic therapy emerges from the new concepts of neuroplasticity. One of the most innovative contributions in this field is robotic exoskeletons. However, there is not enough scientific evidence about its clinical use. The objective of this proposal is to assess the effectiveness of a new model of robotic exoskeleton (Exo H2)...) |
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The recovery of walking capacity is one of the main objectives of rehabilitation in people with incomplete spinal injury. Robotic therapy emerges from the new concepts of neuroplasticity. One of the most innovative contributions in this field is robotic exoskeletons. However, there is not enough scientific evidence about its clinical use. The objective of this proposal is to assess the effectiveness of a new model of robotic exoskeleton (Exo H2) developed by the CSIC and in which the HNP participated in the context of the project HYPER of the Consolider 2009 call for the rehabilitation of the march of people with incomplete spinal injury. For this purpose, a multicenter study is proposed, in which the National Hospital of Paraplegics and the Guttmann Institute will participate. 2 groups of randomised patients with an incomplete spinal lesion in subacute phase who can initiate re-education of the gait will be obtained. In one group, a march rehabilitation protocol based on Exo H2 will be applied, and in the other group the traditional therapy that will act as a control group will be applied. Both patient groups will be evaluated for a physical examination including functional gait scales (10 MWT, 6mWT, WISCI, SCIM) and a biomechanical gait analysis using kinetic and kinematic techniques. An initial evaluation will be performed, another at the end of the procedure and another 6 weeks after the end of the treatment. (English) | |||||||||||||||
Property / summary: The recovery of walking capacity is one of the main objectives of rehabilitation in people with incomplete spinal injury. Robotic therapy emerges from the new concepts of neuroplasticity. One of the most innovative contributions in this field is robotic exoskeletons. However, there is not enough scientific evidence about its clinical use. The objective of this proposal is to assess the effectiveness of a new model of robotic exoskeleton (Exo H2) developed by the CSIC and in which the HNP participated in the context of the project HYPER of the Consolider 2009 call for the rehabilitation of the march of people with incomplete spinal injury. For this purpose, a multicenter study is proposed, in which the National Hospital of Paraplegics and the Guttmann Institute will participate. 2 groups of randomised patients with an incomplete spinal lesion in subacute phase who can initiate re-education of the gait will be obtained. In one group, a march rehabilitation protocol based on Exo H2 will be applied, and in the other group the traditional therapy that will act as a control group will be applied. Both patient groups will be evaluated for a physical examination including functional gait scales (10 MWT, 6mWT, WISCI, SCIM) and a biomechanical gait analysis using kinetic and kinematic techniques. An initial evaluation will be performed, another at the end of the procedure and another 6 weeks after the end of the treatment. (English) / rank | |||||||||||||||
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Property / summary: The recovery of walking capacity is one of the main objectives of rehabilitation in people with incomplete spinal injury. Robotic therapy emerges from the new concepts of neuroplasticity. One of the most innovative contributions in this field is robotic exoskeletons. However, there is not enough scientific evidence about its clinical use. The objective of this proposal is to assess the effectiveness of a new model of robotic exoskeleton (Exo H2) developed by the CSIC and in which the HNP participated in the context of the project HYPER of the Consolider 2009 call for the rehabilitation of the march of people with incomplete spinal injury. For this purpose, a multicenter study is proposed, in which the National Hospital of Paraplegics and the Guttmann Institute will participate. 2 groups of randomised patients with an incomplete spinal lesion in subacute phase who can initiate re-education of the gait will be obtained. In one group, a march rehabilitation protocol based on Exo H2 will be applied, and in the other group the traditional therapy that will act as a control group will be applied. Both patient groups will be evaluated for a physical examination including functional gait scales (10 MWT, 6mWT, WISCI, SCIM) and a biomechanical gait analysis using kinetic and kinematic techniques. An initial evaluation will be performed, another at the end of the procedure and another 6 weeks after the end of the treatment. (English) / qualifier | |||||||||||||||
point in time: 12 October 2021
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Revision as of 13:57, 12 October 2021
Project Q3142425 in Spain
Language | Label | Description | Also known as |
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English | No label defined |
Project Q3142425 in Spain |
Statements
65,200.0 Euro
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81,500.0 Euro
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80.0 percent
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1 January 2016
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16 December 2018
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FUNDACION DEL HOSPITAL NACIONAL DE PARAPLEJICOS
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45168
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La recuperación de la capacidad de deambulación es uno de los principales objetivos de la rehabilitación en personas con lesión medular incompleta. De la mano de los nuevos conceptos de neuroplasticidad surge la terapia robótica. Uno de las aportaciones más novedosas en este campo son los exoesqueletos robotizados. Sin embargo, no hay suficiente evidencia científica sobre su uso clínico. El objetivo de esta propuesta es valorar la eficacia de un nuevo modelo de exoesqueleto robotizado (Exo H2) desarrollado por el CSIC y en cuyo desarrollo participó el HNP en el contexto del proyecto HYPER de la convocatoria Consolider 2009 en la rehabilitación de la marcha de las personas con lesión medular incompleta. Para ello, se propone un estudio multicéntrico, en el que participarán el Hospital Nacional de Parapléjicos y el Institut Guttmann. Se obtendrán 2 grupos de pacientes aleatorizados con una lesión medular incompleta en fase subaguda que puedan iniciar la reeeducación de la marcha. En un grupo se aplicará un protocolo de rehabilitación de la marcha basado en el Exo H2 y en el otro se aplicará la terapia tradicional que actuará como grupo control. A ambos grupos de pacientes se les evaluará realizando un examen físico incluyendo escalas funcionales de la marcha (10 MWT, 6mWT, WISCI, SCIM) y un análisis biomecánico de la marcha con técnicas cinéticas y cinemáticas. Se realizará una evaluación inicial, otra al finalizar la intervención y otra 6 semanas después de terminado el tratamiento. (Spanish)
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The recovery of walking capacity is one of the main objectives of rehabilitation in people with incomplete spinal injury. Robotic therapy emerges from the new concepts of neuroplasticity. One of the most innovative contributions in this field is robotic exoskeletons. However, there is not enough scientific evidence about its clinical use. The objective of this proposal is to assess the effectiveness of a new model of robotic exoskeleton (Exo H2) developed by the CSIC and in which the HNP participated in the context of the project HYPER of the Consolider 2009 call for the rehabilitation of the march of people with incomplete spinal injury. For this purpose, a multicenter study is proposed, in which the National Hospital of Paraplegics and the Guttmann Institute will participate. 2 groups of randomised patients with an incomplete spinal lesion in subacute phase who can initiate re-education of the gait will be obtained. In one group, a march rehabilitation protocol based on Exo H2 will be applied, and in the other group the traditional therapy that will act as a control group will be applied. Both patient groups will be evaluated for a physical examination including functional gait scales (10 MWT, 6mWT, WISCI, SCIM) and a biomechanical gait analysis using kinetic and kinematic techniques. An initial evaluation will be performed, another at the end of the procedure and another 6 weeks after the end of the treatment. (English)
12 October 2021
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Toledo
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Identifiers
PI15_01437
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