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The ReWalk ReStore™ soft robotic exosuit: a multi-site clinical trial of the safety, reliability, and feasibility of exosuit-augmented post-stroke gait rehabilitation.
Awad, Louis N; Esquenazi, Alberto; Francisco, Gerard E; Nolan, Karen J; Jayaraman, Arun.
Afiliación
  • Awad LN; Department of Physical Therapy & Athletic Training, Boston University, Boston, MA, USA. louawad@bu.edu.
  • Esquenazi A; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA. louawad@bu.edu.
  • Francisco GE; Department of PM&R, Harvard Medical School, Spaulding Rehabilitation Hospital, Boston, MA, USA. louawad@bu.edu.
  • Nolan KJ; Department of PM&R, MossRehab and Einstein Healthcare Network, Elkins Park, PA, USA.
  • Jayaraman A; Department of PM&R, University of Texas McGovern Medical School, TIRR Memorial Hermann, Houston, TX, USA.
J Neuroeng Rehabil ; 17(1): 80, 2020 06 18.
Article en En | MEDLINE | ID: mdl-32552775
ABSTRACT

BACKGROUND:

Atypical walking in the months and years after stroke constrain community reintegration and reduce mobility, health, and quality of life. The ReWalk ReStore™ is a soft robotic exosuit designed to assist the propulsion and ground clearance subtasks of post-stroke walking by actively assisting paretic ankle plantarflexion and dorsiflexion. Previous proof-of-concept evaluations of the technology demonstrated improved gait mechanics and energetics and faster and farther walking in users with post-stroke hemiparesis. We sought to determine the safety, reliability, and feasibility of using the ReStore™ during post-stroke rehabilitation.

METHODS:

A multi-site clinical trial (NCT03499210) was conducted in preparation for an application to the United States Food and Drug Administration (FDA). The study included 44 users with post-stroke hemiparesis who completed up to 5 days of training with the ReStore™ on the treadmill and over ground. In addition to primary and secondary endpoints of safety and device reliability across all training activities, an exploratory evaluation of the effect of multiple exposures to using the device on users' maximum walking speeds with and without the device was conducted prior to and following the five training visits.

RESULTS:

All 44 study participants completed safety and reliability evaluations. Thirty-six study participants completed all five training days. No device-related falls or serious adverse events were reported. A low rate of device malfunctions was reported by clinician-operators. Regardless of their reliance on ancillary assistive devices, after only 5 days of walking practice with the device, study participants increased both their device-assisted (Δ 0.10 ± 0.03 m/s) and unassisted (Δ 0.07 ± 0.03 m/s) maximum walking speeds (P's < 0.05).

CONCLUSIONS:

When used under the direction of a licensed physical therapist, the ReStore™ soft exosuit is safe and reliable for use during post-stroke gait rehabilitation to provide targeted assistance of both paretic ankle plantarflexion and dorsiflexion during treadmill and overground walking. TRIAL REGISTRATION NCT03499210. Prospectively registered on March 28, 2018.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Robótica / Trastornos Neurológicos de la Marcha / Dispositivo Exoesqueleto / Rehabilitación de Accidente Cerebrovascular Tipo de estudio: Clinical_trials / Etiology_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neuroeng Rehabil Asunto de la revista: ENGENHARIA BIOMEDICA / NEUROLOGIA / REABILITACAO Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Robótica / Trastornos Neurológicos de la Marcha / Dispositivo Exoesqueleto / Rehabilitación de Accidente Cerebrovascular Tipo de estudio: Clinical_trials / Etiology_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neuroeng Rehabil Asunto de la revista: ENGENHARIA BIOMEDICA / NEUROLOGIA / REABILITACAO Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos