Study protocol - robot-assisted gait therapy using Lokomat Pro FreeD in patients in the subacute phase of ischemic stroke
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F21%3AA2202DCI" target="_blank" >RIV/61988987:17110/21:A2202DCI - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61988987:17110/21:A2302HL8
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>
Alternativní jazyky
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).
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30103 - Neurosciences (including psychophysiology)
Návaznosti výsledku
Projekt
—
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2021
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Ceska a Slovenska Neurologie a Neurochirurgie
ISSN
1210-7859
e-ISSN
—
Svazek periodika
84
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
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