Study protocol - robot-assisted gait therapy using Lokomat Pro FreeD in patients in the subacute phase of ischemic stroke

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F21%3AA2302HL8" target="_blank" >RIV/61988987:17110/21:A2302HL8 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61988987:17110/21:A2202DCI

Výsledek na webu

<a href="https://www.webofscience.com/wos/woscc/full-record/WOS:000738908000008" target="_blank" >https://www.webofscience.com/wos/woscc/full-record/WOS:000738908000008</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.48095/cccsnn2021361" target="_blank" >10.48095/cccsnn2021361</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Study protocol - robot-assisted gait therapy using Lokomat Pro FreeD in patients in the subacute phase of ischemic stroke

Popis výsledku v původním jazyce

Aim: Robot-assisted gait training represents a modern concept of neurorehabilitation in stroke patients. Our randomized interventional study aims to assess the additive effect of robot-assisted gait rehabilitation in subacute ischemic stroke patients and to compare its effect with patients undergoing standard institutional protocol-defi ned rehabilitation. The primary endpoint is the functional ambulation category. The secondary endpoints include gait time parameters (10 Meter Walk Test, Timed Up and Go), changes in body composition, modifi ed Rankin scale, Barthel index, Berg balance scale, and a questionnaire Falls Efficacy Scale - International. Radiological sub study evaluates the dynamics of brain structural changes and atrophy using MRI. Methods: This is a prospective randomized open monocentric study enrolling patients within 6 weeks from the onset of the firs ischemic stroke. Both groups are treated with conventional rehabilitation (physiotherapy, occupational therapy and mechanotherapy) for 60 min 5 times a week, a total of 15 times for 3 to 4 weeks (a total of 1,200 min). The Lokomat group undergoes robot-assisted gait training using the interventional exoskeleton for 20-50 minutes 5 times a week for a total of 15 times for 3 to 4 weeks (a total of 1,800 min). Data collection takes place over four time periods: pre-intervention (T0), mid-intervention (T1; day 8), post-rehabilitation assessment (T2; day 15), and 3 months post-intervention (T3).

Název v anglickém jazyce

Study protocol - robot-assisted gait therapy using Lokomat Pro FreeD in patients in the subacute phase of ischemic stroke

Popis výsledku anglicky

Aim: Robot-assisted gait training represents a modern concept of neurorehabilitation in stroke patients. Our randomized interventional study aims to assess the additive effect of robot-assisted gait rehabilitation in subacute ischemic stroke patients and to compare its effect with patients undergoing standard institutional protocol-defi ned rehabilitation. The primary endpoint is the functional ambulation category. The secondary endpoints include gait time parameters (10 Meter Walk Test, Timed Up and Go), changes in body composition, modifi ed Rankin scale, Barthel index, Berg balance scale, and a questionnaire Falls Efficacy Scale - International. Radiological sub study evaluates the dynamics of brain structural changes and atrophy using MRI. Methods: This is a prospective randomized open monocentric study enrolling patients within 6 weeks from the onset of the firs ischemic stroke. Both groups are treated with conventional rehabilitation (physiotherapy, occupational therapy and mechanotherapy) for 60 min 5 times a week, a total of 15 times for 3 to 4 weeks (a total of 1,200 min). The Lokomat group undergoes robot-assisted gait training using the interventional exoskeleton for 20-50 minutes 5 times a week for a total of 15 times for 3 to 4 weeks (a total of 1,800 min). Data collection takes place over four time periods: pre-intervention (T0), mid-intervention (T1; day 8), post-rehabilitation assessment (T2; day 15), and 3 months post-intervention (T3).

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30103 - Neurosciences (including psychophysiology)

Projekt

—

Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2021

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Ceska a Slovenska Neurologie a Neurochirurgie

ISSN

1210-7859

e-ISSN

—

Svazek periodika

—

Číslo periodika v rámci svazku

4

Stát vydavatele periodika

CZ - Česká republika

Počet stran výsledku

6

Strana od-do

361-366

Kód UT WoS článku

000738908000008

EID výsledku v databázi Scopus

—