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Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?

Studies using transcranial direct current stimulation (tDCS) typically incorporate a fade‐in, short‐stimulation, fade‐out sham (placebo) protocol, which is assumed to be indistinct from a 10–30 min active protocol on the scalp. However, many studies report that participants can dissociate active sti...

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Detalles Bibliográficos
Autores principales: Turner, Christopher, Jackson, Catherine, Learmonth, Gemma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048983/
https://www.ncbi.nlm.nih.gov/pubmed/33098709
http://dx.doi.org/10.1111/ejn.15018
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author Turner, Christopher
Jackson, Catherine
Learmonth, Gemma
author_facet Turner, Christopher
Jackson, Catherine
Learmonth, Gemma
author_sort Turner, Christopher
collection PubMed
description Studies using transcranial direct current stimulation (tDCS) typically incorporate a fade‐in, short‐stimulation, fade‐out sham (placebo) protocol, which is assumed to be indistinct from a 10–30 min active protocol on the scalp. However, many studies report that participants can dissociate active stimulation from sham, even during low‐intensity 1 mA currents. We recently identified differences in the perception of an active (10 min of 1 mA) and a sham (20 s of 1 mA) protocol that lasted for 5 min after the cessation of sham. In the present study we assessed whether delivery of a higher‐intensity 2 mA current would exacerbate these differences. Two protocols were delivered to 32 adults in a double‐blinded, within‐subjects design (active: 10 min of 2 mA, and sham: 20 s of 2 mA), with the anode over the left primary motor cortex and the cathode on the right forehead. Participants were asked “Is the stimulation on?” and “How sure are you?” at 30 s intervals during and after stimulation. The differences between active and sham were more consistent and sustained during 2 mA than during 1 mA. We then quantified how well participants were able to track the presence and absence of stimulation (i.e. their sensitivity) during the experiment using cross‐correlations. Current strength was a good classifier of sensitivity during active tDCS, but exhibited only moderate specificity during sham. The accuracy of the end‐of‐study guess was no better than chance at predicting sensitivity. Our results indicate that the traditional end‐of‐study guess poorly reflects the sensitivity of participants to stimulation, and may not be a valid method of assessing sham blinding.
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spelling pubmed-80489832021-04-20 Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation? Turner, Christopher Jackson, Catherine Learmonth, Gemma Eur J Neurosci Systems Neuroscience Studies using transcranial direct current stimulation (tDCS) typically incorporate a fade‐in, short‐stimulation, fade‐out sham (placebo) protocol, which is assumed to be indistinct from a 10–30 min active protocol on the scalp. However, many studies report that participants can dissociate active stimulation from sham, even during low‐intensity 1 mA currents. We recently identified differences in the perception of an active (10 min of 1 mA) and a sham (20 s of 1 mA) protocol that lasted for 5 min after the cessation of sham. In the present study we assessed whether delivery of a higher‐intensity 2 mA current would exacerbate these differences. Two protocols were delivered to 32 adults in a double‐blinded, within‐subjects design (active: 10 min of 2 mA, and sham: 20 s of 2 mA), with the anode over the left primary motor cortex and the cathode on the right forehead. Participants were asked “Is the stimulation on?” and “How sure are you?” at 30 s intervals during and after stimulation. The differences between active and sham were more consistent and sustained during 2 mA than during 1 mA. We then quantified how well participants were able to track the presence and absence of stimulation (i.e. their sensitivity) during the experiment using cross‐correlations. Current strength was a good classifier of sensitivity during active tDCS, but exhibited only moderate specificity during sham. The accuracy of the end‐of‐study guess was no better than chance at predicting sensitivity. Our results indicate that the traditional end‐of‐study guess poorly reflects the sensitivity of participants to stimulation, and may not be a valid method of assessing sham blinding. John Wiley and Sons Inc. 2020-11-20 2021-03 /pmc/articles/PMC8048983/ /pubmed/33098709 http://dx.doi.org/10.1111/ejn.15018 Text en © 2020 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Systems Neuroscience
Turner, Christopher
Jackson, Catherine
Learmonth, Gemma
Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?
title Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?
title_full Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?
title_fullStr Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?
title_full_unstemmed Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?
title_short Is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?
title_sort is the “end‐of‐study guess” a valid measure of sham blinding during transcranial direct current stimulation?
topic Systems Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048983/
https://www.ncbi.nlm.nih.gov/pubmed/33098709
http://dx.doi.org/10.1111/ejn.15018
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