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      Blocked versus randomized presentation modes differentially modulate feedback-related negativity and P3b amplitudes

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          Highlights

          • ERP responses to feedback stimuli with explicit or assigned valence information were investigated with blocked or randomized trial presentation modes.

          • Only P3b, but not feedback-related negativity amplitudes were affected by feedback type for both presentation modes.

          • Results suggest using blocked design when using different types of feedback stimuli.

          Abstract

          Objective

          Electrophysiological studies on feedback processing typically use a wide range of feedback stimuli which might not always be comparable. The current study investigated whether two indicators of feedback processing – feedback-related negativity (FRN) and P3b – differ for feedback stimuli with explicit (facial expressions) or assigned valence information (symbols). In addition, we assessed whether presenting feedback in either a trial-by-trial or a block-wise fashion affected these ERPs.

          Methods

          EEG was recorded in three experiments while participants performed a time estimation task and received two different types of performance feedback.

          Results

          Only P3b amplitudes varied consistently in response to feedback type for both presentation types. Moreover, the blocked feedback type presentation yielded more distinct FRN peaks, higher effect sizes, and a significant relation between FRN amplitudes and behavioral task performance measures.

          Conclusion

          Both stimulus type and presentation mode may provoke systematic changes in feedback-related ERPs. The current findings point at important potential confounds that need to be controlled for when designing FRN or P3b studies.

          Significance

          Studies investigating P3b amplitudes using mixed types of stimuli have to be interpreted with caution. Furthermore, we suggest implementing a blocked presentation format when presenting different feedback types within the same experiment.

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          Most cited references47

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          Bad is stronger than good.

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            The neural basis of human error processing: reinforcement learning, dopamine, and the error-related negativity.

            The authors present a unified account of 2 neural systems concerned with the development and expression of adaptive behaviors: a mesencephalic dopamine system for reinforcement learning and a "generic" error-processing system associated with the anterior cingulate cortex. The existence of the error-processing system has been inferred from the error-related negativity (ERN), a component of the event-related brain potential elicited when human participants commit errors in reaction-time tasks. The authors propose that the ERN is generated when a negative reinforcement learning signal is conveyed to the anterior cingulate cortex via the mesencephalic dopamine system and that this signal is used by the anterior cingulate cortex to modify performance on the task at hand. They provide support for this proposal using both computational modeling and psychophysiological experimentation.
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              Decision making, the P3, and the locus coeruleus-norepinephrine system.

              Psychologists and neuroscientists have had a long-standing interest in the P3, a prominent component of the event-related brain potential. This review aims to integrate knowledge regarding the neural basis of the P3 and to elucidate its functional role in information processing. The authors review evidence suggesting that the P3 reflects phasic activity of the neuromodulatory locus coeruleus-norepinephrine (LC-NE) system. They discuss the P3 literature in the light of empirical findings and a recent theory regarding the information-processing function of the LC-NE phasic response. The theoretical framework emerging from this research synthesis suggests that the P3 reflects the response of the LC-NE system to the outcome of internal decision-making processes and the consequent effects of noradrenergic potentiation of information processing. Copyright 2005 APA, all rights reserved.
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                Author and article information

                Contributors
                Journal
                Clin Neurophysiol
                Clin Neurophysiol
                Clinical Neurophysiology
                Elsevier
                1388-2457
                1872-8952
                1 April 2014
                April 2014
                : 125
                : 4
                : 715-726
                Affiliations
                [a ]Social, Cognitive and Affective Neuroscience Unit, Department of Basic Psychological Research and Research Methods, Faculty of Psychology, University of Vienna, Liebiggasse 5, A-1010 Vienna, Austria
                [b ]Department of Psychology, Faculty of Social Sciences, University of Gothenburg, Haraldsgatan 1, SE-40530 Gothenburg, Sweden
                Author notes
                [* ]Corresponding author. Tel.: +43 1 4277 47132; fax: +43 1 4277 47193. daniela.pfabigan@ 123456univie.ac.at
                Article
                S1388-2457(13)01092-4
                10.1016/j.clinph.2013.09.029
                3947619
                24144779
                583e196b-f3ac-4be7-a54a-3cf6df488680
                © 2013 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
                History
                : 21 September 2013
                Categories
                Article

                Neurology
                frn,p3b,feedback stimulus characteristics,presentation mode
                Neurology
                frn, p3b, feedback stimulus characteristics, presentation mode

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