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Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects

BACKGROUND: Transcutaneous neurostimulation (TNS) at extracephalic sites is a well known treatment of pain. Thanks to recent technical progress, the Cefaly(® )device now also allows supraorbital TNS. During observational clinical studies, several patients reported decreased vigilance or even sleepin...

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Autores principales: Piquet, Maxime, Balestra, Costantino, Sava, Simona L, Schoenen, Jean E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261828/
https://www.ncbi.nlm.nih.gov/pubmed/22035386
http://dx.doi.org/10.1186/1471-2377-11-135
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author Piquet, Maxime
Balestra, Costantino
Sava, Simona L
Schoenen, Jean E
author_facet Piquet, Maxime
Balestra, Costantino
Sava, Simona L
Schoenen, Jean E
author_sort Piquet, Maxime
collection PubMed
description BACKGROUND: Transcutaneous neurostimulation (TNS) at extracephalic sites is a well known treatment of pain. Thanks to recent technical progress, the Cefaly(® )device now also allows supraorbital TNS. During observational clinical studies, several patients reported decreased vigilance or even sleepiness during a session of supraorbital TNS. We decided therefore to explore in more detail the potential sedative effect of supraorbital TNS, using standardized psychophysical tests in healthy volunteers. METHODS: We performed a double-blind cross-over sham-controlled study on 30 healthy subjects. They underwent a series of 4 vigilance tests (Psychomotor Vigilance Task, Critical Flicker Fusion Frequency, Fatigue Visual Numeric Scale, d2 test). Each subject was tested under 4 different experimental conditions: without the neurostimulation device, with sham supraorbital TNS, with low frequency supraorbital TNS and with high frequency supraorbital TNS. RESULTS: As judged by the results of three tests (Psychomotor Vigilance Task, Critical Flicker Fusion Frequency, Fatigue Visual Numeric Scale) there was a statistically significant (p < 0.001) decrease in vigilance and attention during high frequency TNS, while there were no changes during the other experimental conditions. Similarly, performance on the d2 test was impaired during high frequency TNS, but this change was not statistically significant. CONCLUSION: Supraorbital high frequency TNS applied with the Cefaly(® )device decreases vigilance in healthy volunteers. Additional studies are needed to determine the duration of this effect, the underlying mechanisms and the possible relation with the stimulation parameters. Meanwhile, this effect opens interesting perspectives for the treatment of hyperarousal states and, possibly, insomnia.
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spelling pubmed-32618282012-01-20 Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects Piquet, Maxime Balestra, Costantino Sava, Simona L Schoenen, Jean E BMC Neurol Research Article BACKGROUND: Transcutaneous neurostimulation (TNS) at extracephalic sites is a well known treatment of pain. Thanks to recent technical progress, the Cefaly(® )device now also allows supraorbital TNS. During observational clinical studies, several patients reported decreased vigilance or even sleepiness during a session of supraorbital TNS. We decided therefore to explore in more detail the potential sedative effect of supraorbital TNS, using standardized psychophysical tests in healthy volunteers. METHODS: We performed a double-blind cross-over sham-controlled study on 30 healthy subjects. They underwent a series of 4 vigilance tests (Psychomotor Vigilance Task, Critical Flicker Fusion Frequency, Fatigue Visual Numeric Scale, d2 test). Each subject was tested under 4 different experimental conditions: without the neurostimulation device, with sham supraorbital TNS, with low frequency supraorbital TNS and with high frequency supraorbital TNS. RESULTS: As judged by the results of three tests (Psychomotor Vigilance Task, Critical Flicker Fusion Frequency, Fatigue Visual Numeric Scale) there was a statistically significant (p < 0.001) decrease in vigilance and attention during high frequency TNS, while there were no changes during the other experimental conditions. Similarly, performance on the d2 test was impaired during high frequency TNS, but this change was not statistically significant. CONCLUSION: Supraorbital high frequency TNS applied with the Cefaly(® )device decreases vigilance in healthy volunteers. Additional studies are needed to determine the duration of this effect, the underlying mechanisms and the possible relation with the stimulation parameters. Meanwhile, this effect opens interesting perspectives for the treatment of hyperarousal states and, possibly, insomnia. BioMed Central 2011-10-28 /pmc/articles/PMC3261828/ /pubmed/22035386 http://dx.doi.org/10.1186/1471-2377-11-135 Text en Copyright ©2011 Piquet et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Piquet, Maxime
Balestra, Costantino
Sava, Simona L
Schoenen, Jean E
Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects
title Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects
title_full Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects
title_fullStr Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects
title_full_unstemmed Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects
title_short Supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects
title_sort supraorbital transcutaneous neurostimulation has sedative effects in healthy subjects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261828/
https://www.ncbi.nlm.nih.gov/pubmed/22035386
http://dx.doi.org/10.1186/1471-2377-11-135
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