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A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis

Model-based analysis of skin conductance responses (SCR) can furnish less noisy estimates of sympathetic arousal (SA) than operational peak scoring approaches, as shown in previous work. Here, I compare two model-based methods for analysis of evoked (stimulus-locked) SCR, implemented in two software...

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Autor principal: Bach, Dominik R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266536/
https://www.ncbi.nlm.nih.gov/pubmed/25148785
http://dx.doi.org/10.1016/j.biopsycho.2014.08.006
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author Bach, Dominik R.
author_facet Bach, Dominik R.
author_sort Bach, Dominik R.
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description Model-based analysis of skin conductance responses (SCR) can furnish less noisy estimates of sympathetic arousal (SA) than operational peak scoring approaches, as shown in previous work. Here, I compare two model-based methods for analysis of evoked (stimulus-locked) SCR, implemented in two software packages, SCRalyze and Ledalab, with respect to their sensitivity in recovering SA. Four datasets are analysed to compare predictive validity, i.e. the sensitivity to distinguish pairs of SA states that are known to be different. SCRalyze was significantly better able than Ledalab to recover this known difference in four out of five tested contrasts and comparable in the remaining one. SCRalyze performed significantly better than conventional analysis in all contrasts. I conclude that the model-based method engendered in SCRalyze is currently the best available approach to provide robust and sensitive estimates of sympathetic arousal.
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spelling pubmed-42665362014-12-16 A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis Bach, Dominik R. Biol Psychol Article Model-based analysis of skin conductance responses (SCR) can furnish less noisy estimates of sympathetic arousal (SA) than operational peak scoring approaches, as shown in previous work. Here, I compare two model-based methods for analysis of evoked (stimulus-locked) SCR, implemented in two software packages, SCRalyze and Ledalab, with respect to their sensitivity in recovering SA. Four datasets are analysed to compare predictive validity, i.e. the sensitivity to distinguish pairs of SA states that are known to be different. SCRalyze was significantly better able than Ledalab to recover this known difference in four out of five tested contrasts and comparable in the remaining one. SCRalyze performed significantly better than conventional analysis in all contrasts. I conclude that the model-based method engendered in SCRalyze is currently the best available approach to provide robust and sensitive estimates of sympathetic arousal. Elsevier Science B.V 2014-12 /pmc/articles/PMC4266536/ /pubmed/25148785 http://dx.doi.org/10.1016/j.biopsycho.2014.08.006 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Bach, Dominik R.
A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis
title A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis
title_full A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis
title_fullStr A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis
title_full_unstemmed A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis
title_short A head-to-head comparison of SCRalyze and Ledalab, two model-based methods for skin conductance analysis
title_sort head-to-head comparison of scralyze and ledalab, two model-based methods for skin conductance analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266536/
https://www.ncbi.nlm.nih.gov/pubmed/25148785
http://dx.doi.org/10.1016/j.biopsycho.2014.08.006
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