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dc.contributor.authorKarl, A
dc.contributor.authorCarnelley, KB
dc.contributor.authorArikan, G
dc.contributor.authorBaldwin, DS
dc.contributor.authorHeinrichs, M
dc.contributor.authorStopa, L
dc.date.accessioned2021-03-09T14:29:29Z
dc.date.issued2021-03-13
dc.description.abstractTo further understand protective mechanisms to prevent post-traumatic stress disorder or assist recovery from psychological trauma, this study investigated whether pharmacological and psychological activation of a secure attachment representation elicits higher felt-security and a related response pattern of reduced physiological arousal and increased parasympathetic activation; and whether it protects individuals from developing intrusions and experiencing distress in the week following exposure to a trauma film. Using a double-blind, experimental mixed factorial design, 101 volunteers received either oxytocin or placebo and either secure attachment or neutral priming before watching a trauma film. We measured felt security as an indicator of the strength of activation of a secure attachment representation, skin conductance and heart rate as indicators of physiological arousal, and high frequency heart rate variability as an indicator of parasympathetic activation during the priming and the film. Participants then completed a seven-day intrusion diary. Secure attachment priming, but not oxytocin administration or the combination of both, was associated with reduced physiological arousal and increased parasympathetic activity during priming. Although secure attachment priming was not related to the absolute number of intrusions or to less perceived distress or physiological arousal during the trauma film, it was associated with lower intrusion-related distress in the 7-days post-testing. Our findings extend previous research that suggests the importance of interventions that address intrusion-related distress for recovery from trauma, and suggest a promising role for secure attachment priming in trauma-focused psychological therapies. We contribute to the growing literature that finds that higher subjective distress during a trauma is associated with higher intrusion-related distress. We discuss theoretical implications and possible mechanisms through which secure attachment priming may exert potential beneficial effects.en_GB
dc.description.sponsorshipOverseas Research Students Awards Scheme (ORSAS)en_GB
dc.description.sponsorshipCompassionate Mind Foundationen_GB
dc.identifier.citationArticle 103845en_GB
dc.identifier.doi10.1016/j.brat.2021.103845
dc.identifier.urihttp://hdl.handle.net/10871/125075
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rights.embargoreasonUnder embargo until 13 March 2023 in compliance with publisher policyen_GB
dc.rights© 2021. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  en_GB
dc.subjectoxytocinen_GB
dc.subjectattachment primingen_GB
dc.subjecttrauma film paradigmen_GB
dc.subjectpsychophysiologyen_GB
dc.subjectintrusionsen_GB
dc.titleThe Effect of Attachment Security Priming and Oxytocin on Physiological Responses to Trauma Films and Subsequent Intrusionsen_GB
dc.typeArticleen_GB
dc.date.available2021-03-09T14:29:29Z
dc.identifier.issn0005-7967
dc.descriptionThis is the author accepted manuscript. The final version is available from Elsevier via the DOI in this recorden_GB
dc.identifier.journalBehaviour Research and Therapyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/  en_GB
dcterms.dateAccepted2021-03-08
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2021-03-08
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2021-03-09T12:51:45Z
refterms.versionFCDAM
refterms.dateFOA2023-03-13T00:00:00Z
refterms.panelAen_GB


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© 2021. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  
Except where otherwise noted, this item's licence is described as © 2021. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/