Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/94307
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dc.contributorDepartment of Biomedical Engineering-
dc.creatorMcGeady, C-
dc.creatorAlam, M-
dc.creatorZheng, YP-
dc.creatorVučković, A-
dc.date.accessioned2022-08-11T02:01:46Z-
dc.date.available2022-08-11T02:01:46Z-
dc.identifier.urihttp://hdl.handle.net/10397/94307-
dc.language.isoenen_US
dc.publisherMolecular Diversity Preservation International (MDPI)en_US
dc.rights© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication McGeady, C., Alam, M., Zheng, Y. P., & Vučković, A. (2022). Effect of Cervical Transcutaneous Spinal Cord Stimulation on Sensorimotor Cortical Activity during Upper-Limb Movements in Healthy Individuals. Journal of Clinical Medicine, 11(4), 1043 is available at https://doi.org/10.3390/jcm11041043en_US
dc.subjectElectroencephalographyen_US
dc.subjectEvent-related desynchronisationen_US
dc.subjectNeuromodulationen_US
dc.subjectPosterior root muscle reflexen_US
dc.subjectRehabilitationen_US
dc.subjectTranscutaneous spinal cord stimulationen_US
dc.titleEffect of cervical transcutaneous spinal cord stimulation on sensorimotor cortical activity during upper-limb movements in healthy individualsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume11-
dc.identifier.issue4-
dc.identifier.doi10.3390/jcm11041043-
dcterms.abstractTranscutaneous spinal cord stimulation (tSCS) can improve upper-limb motor function after spinal cord injury. A number of studies have attempted to deduce the corticospinal mechanisms which are modulated following tSCS, with many relying on transcranial magnetic stimulation to provide measures of corticospinal excitability. Other metrics, such as cortical oscillations, may provide an alternative and complementary perspective on the physiological effect of tSCS. Hence, the present study recorded EEG from 30 healthy volunteers to investigate if and how cortical oscillatory dynamics are altered by 10 min of continuous cervical tSCS. Participants performed repetitive upper-limb movements and resting-state tasks while tSCS was delivered to the posterior side of the neck as EEG was recorded simultaneously. The intensity of tSCS was tailored to each participant based on their maximum tolerance (mean: 50 ± 20 mA). A control session was conducted without tSCS. Changes to sensorimotor cortical activity during movement were quantified in terms of eventrelated (de)synchronisation (ERD/ERS). Our analysis revealed that, on a group level, there was no consistency in terms of the direction of ERD modulation during tSCS, nor was there a dose-effect between tSCS and ERD/ERS. Resting-state oscillatory power was compared before and after tSCS but no statistically significant difference was found in terms of alpha peak frequency or alpha power. However, participants who received the highest stimulation intensities had significantly weakened ERD/ERS (10% ERS) compared to when tSCS was not applied (25% ERD; p = 0.016), suggestive of cortical inhibition. Overall, our results demonstrated that a single 10 min session of tSCS delivered to the cervical region of the spine was not sufficient to induce consistent changes in sensorimotor cortical activity among the entire cohort. However, under high intensities there may be an inhibitory effect at the cortical level. Future work should investigate, with a larger sample size, the effect of session duration and tSCS intensity on cortical oscillations.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of clinical medicine, Feb. 2022, v. 11, no. 4, 1043-
dcterms.isPartOfJournal of clinical medicine-
dcterms.issued2022-02-
dc.identifier.scopus2-s2.0-85124579063-
dc.identifier.eissn2077-0383-
dc.identifier.artn1043-
dc.description.validate202208 bckw-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera1628en_US
dc.identifier.SubFormID45655en_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextDepartmental General Research Fund; Telefield Charitable Funden_US
dc.description.pubStatusPublisheden_US
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