Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/41338
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dc.contributor.authorMendes, Augusto J.pt_PT
dc.contributor.authorLema, Albertopt_PT
dc.contributor.authorCarvalho, Sandrapt_PT
dc.contributor.authorLeite, Jorgept_PT
dc.date.accessioned2024-04-03T14:24:30Z-
dc.date.available2024-04-03T14:24:30Z-
dc.date.issued2024-04-03-
dc.identifier.urihttp://hdl.handle.net/10773/41338-
dc.description.abstractBackground Transcranial alternating current stimulation (tACS) is a brain stimulation method for modulating ongoing endogenous oscillatory activity at specified frequency during sensory and cognitive processes. Given the overlap between event-related potentials (ERPs) and event-related oscillations (EROs), ERPs can be studied as putative biomarkers of the effects of tACS in the brain during cognitive/sensory task performance. Objective This preliminary study aimed to test the feasibility of individually tailored tACS based on individual P3 (latency and frequency) elicited during a cued premature response task. Thus, tACS frequency was individually tailored to match target-P3 ERO for each participant. Likewise, the target onset in the task was adjusted to match the tACS phase and target-P3 latency. Methods Twelve healthy volunteers underwent tACS in two separate sessions while performing a premature response task. Target-P3 latency and ERO were calculated in a baseline block during the first session to allow a posterior synchronization between the tACS and the endogenous oscillatory activity. The cue and target-P3 amplitudes, delta/theta ERO, and power spectral density (PSD) were evaluated pre and post-tACS blocks. Results Target-P3 amplitude significantly increased after activetACS, when compared to sham. Evoked-delta during cue-P3 was decreased after tACS. No effects were found for delta ERO during target-P3 nor for the PSD and behavioral outcomes. Conclusion The present findings highlight the possible effect of phase synchronization between individualized tACS parameters and endogenous oscillatory activity, which may result in an enhancement of the underlying process (i.e., an increase of target-P3). However, an unsuccessful synchronization between tACS and EEG activity might also result in a decrease in the evoked-delta activity during cue-P3. Further studies are needed to optimize the parameters of endogenous activity and tACS synchronization. The implications of the current results for future studies, including clinical studies, are further discussed since transcranial alternating current stimulation can be individually tailored based on endogenous event-related P3 to modulate responses.pt_PT
dc.language.isoengpt_PT
dc.publisherPeerJpt_PT
dc.relationPOCI-01-0145-FEDER-007653pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/Concurso para Financiamento de Projetos de Investigação Científica e Desenvolvimento Tecnológico em Todos os Domínios Científicos - 2017/PTDC%2FPSI-ESP%2F30280%2F2017/PTpt_PT
dc.relationPTDC/PSIESP/29701/2017pt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectNeurosciencept_PT
dc.subjectPsychiatry and psychologypt_PT
dc.subjectHuman-computer interactionpt_PT
dc.titleTailoring transcranial alternating current stimulation based on endogenous event-related P3 to modulate premature responses: a feasibility studypt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.titlePeerJ: Journal of Life & Environmental Sciencespt_PT
degois.publication.volume12pt_PT
dc.identifier.doi10.7717/peerj.17144pt_PT
dc.identifier.essn2167-8359pt_PT
dc.identifier.articlenumbere17144pt_PT
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