Cognition affects gait adaptation after split-belt treadmill training in Parkinson's disease

Split-belt treadmill (SBTM) training has been proposed to improve gait symmetry and overall gait performance of patients with Parkinson's disease (PD). To determine whether patient's baseline features affect gait adaptation to SBTM in PD with freezing of gait (FOG). Twenty participants wit...

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Published inNeurobiology of disease Vol. 181; p. 106109
Main Authors Sasikumar, Sanskriti, Sorrento, Gianluca, Lang, Anthony E., Strafella, Antonio P., Fasano, Alfonso
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.06.2023
Elsevier
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Summary:Split-belt treadmill (SBTM) training has been proposed to improve gait symmetry and overall gait performance of patients with Parkinson's disease (PD). To determine whether patient's baseline features affect gait adaptation to SBTM in PD with freezing of gait (FOG). Twenty participants with idiopathic PD and treatment-resistant FOG underwent several clinical assessments including the Toronto Cognitive Assessment (TorCA) prior to treadmill training. Velocity of the treadmill was adjusted to over-ground walking speed. During SBTM training, the belt velocity on the least-affected side was reduced by 25%. Participants who adapted to SBTM training demonstrated cognitively intact TorCA scores (p < 0.001), particularly intact working memory (p < 0.001). After-effects correlated with normal total TorCA (p = 0.02), working memory and visuospatial (p < 0.001) function. Cognitive impairment, particularly impaired working memory, reduces gait adaptation and after-effects in PD with FOG. This is informative for trials studying prolonged effects of SBTM training in FOG. •A split-belt treadmill (SBTM) can target gait asymmetry in Parkinson's disease.•Gait adaptation to a SBTM relies on intact working memory.•After-effects duration from SBTM training requires intact visuospatial function.•Cognitive status influences trials studying prolonged effects of SBTM training.
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ISSN:0969-9961
1095-953X
DOI:10.1016/j.nbd.2023.106109