Please use this identifier to cite or link to this item:
http://hdl.handle.net/1893/35485
Appears in Collections: | Psychology Journal Articles |
Peer Review Status: | Refereed |
Title: | Non invasive brain stimulation in Stroke patients (NIBS) A prospective randomized open blinded end-point (PROBE) feasibility trial using transcranial direct current stimulation (tDCS) in post stroke hemispatial neglect |
Author(s): | Learmonth, G. Benwell, C.S.Y. Märker, G. Dascalu, D. Checketts, M. Santosh, C. Barber, M. Walters, M. Muir, K.W. Harvey, M. |
Contact Email: | gemma.learmonth@stir.ac.uk |
Issue Date: | 2021 |
Date Deposited: | 20-Oct-2023 |
Citation: | Learmonth G, Benwell C, Märker G, Dascalu D, Checketts M, Santosh C, Barber M, Walters M, Muir K & Harvey M (2021) Non invasive brain stimulation in Stroke patients (NIBS) A prospective randomized open blinded end-point (PROBE) feasibility trial using transcranial direct current stimulation (tDCS) in post stroke hemispatial neglect. <i>Neuropsychological Rehabilitation</i>, 31, pp. 1163-1189. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85086854524&doi=10.1080%2f09602011.2020.1767161&partnerID=40&md5=0ceb5bfb9ae0c887e661a2ada5e04881; https://doi.org/10.1080/09602011.2020.1767161 |
Abstract: | Up to 80% of people who experience a right-hemisphere stroke suffer from hemispatial neglect. This syndrome is debilitating and impedes rehabilitation. We carried out a clinical feasibility trial of transcranial direct current stimulation (tDCS) and a behavioural rehabilitation programme, alone or in combination, in patients with neglect. Patients >4 weeks post right hemisphere stroke were randomized to 10 sessions of tDCS, 10 sessions of a behavioural intervention, combined intervention, or a control task. Primary outcomes were recruitment and retention rates, with secondary outcomes effect sizes on measures of neglect and quality of life, assessed directly after the interventions, and at 6 months follow up. Of 288 confirmed stroke cases referred (representing 7% of confirmed strokes), we randomized 8% (0.6% of stroke cases overall). The largest number of exclusions (91/288 (34%)) were due to medical comorbidities that prevented patients from undergoing 10 intervention sessions. We recruited 24 patients over 29 months, with 87% completing immediate post-intervention and 67% 6 month evaluations. We established poor feasibility of a clinical trial requiring repeated hospital-based tDCS within a UK hospital healthcare setting, either with or without behavioural training, over a sustained time period. Future trials should consider intensity, duration and location of tDCS neglect interventions. |
URL: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85086854524&doi=10.1080%2f09602011.2020.1767161&partnerID=40&md5=0ceb5bfb9ae0c887e661a2ada5e04881 |
DOI Link: | 10.1080/09602011.2020.1767161 |
Rights: | © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis GroupThis is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivativesLicense (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproductionin any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way |
Licence URL(s): | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
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File | Description | Size | Format | |
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Non-invasive brain stimulation in Stroke patients NIBS A prospective randomized open blinded end-point PROBE feasibility trial using transcranial.pdf | Fulltext - Published Version | 3.32 MB | Adobe PDF | View/Open |
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