Oxytocin-Augmented Social Cognitive Skills Training in Schizophrenia
Impairments in social cognition are common in schizophrenia and predict poor functional outcome. The purpose of this proof-of-concept randomized, parallel group clinical trial was to assess whether intranasal oxytocin (OT), given before social cognitive training, enhances learning of social cognitiv...
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description | Impairments in social cognition are common in schizophrenia and predict poor functional outcome. The purpose of this proof-of-concept randomized, parallel group clinical trial was to assess whether intranasal oxytocin (OT), given before social cognitive training, enhances learning of social cognitive skills. Twenty seven male outpatients with schizophrenia participated in a 6-week (12 session) training on social cognitive skills. Training focused on three domains: facial affect recognition, social perception, and empathy. Subjects were randomly assigned (double blind) to receive either intranasal OTor placebo 30 min before each session. Participants did not receive OT between sessions or on the day of assessments. We evaluated scores on social-cognition measures, as well as clinical symptoms and neurocognition, at baseline, 1 week following the final training session, and 1 month later. Our prespecified primary outcome measure was a social-cognition composite score comprised of five individual measures. There were main effects of time (indicating improvement across the combined-treatment groups) on the social-cognition composite score at both 1 week and 1 month following completion of training. Subjects receiving OT demonstrated significantly greater improvements in empathic accuracy than those receiving placebo at both posttreatment and 1 month follow up. There were no OT-related effects for the other social cognitive tests, clinical symptoms, or neurocognition. This study provides initial support for the idea that OT enhances the effectiveness of training when administered shortly before social cognitive training sessions. The effects were most pronounced on empathic accuracy, a high-level social cognitive process that is not easily improved in current social cognitive remediation programs. |
doi_str_mv | 10.1038/npp.2014.68 |
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The purpose of this proof-of-concept randomized, parallel group clinical trial was to assess whether intranasal oxytocin (OT), given before social cognitive training, enhances learning of social cognitive skills. Twenty seven male outpatients with schizophrenia participated in a 6-week (12 session) training on social cognitive skills. Training focused on three domains: facial affect recognition, social perception, and empathy. Subjects were randomly assigned (double blind) to receive either intranasal OTor placebo 30 min before each session. Participants did not receive OT between sessions or on the day of assessments. We evaluated scores on social-cognition measures, as well as clinical symptoms and neurocognition, at baseline, 1 week following the final training session, and 1 month later. Our prespecified primary outcome measure was a social-cognition composite score comprised of five individual measures. There were main effects of time (indicating improvement across the combined-treatment groups) on the social-cognition composite score at both 1 week and 1 month following completion of training. Subjects receiving OT demonstrated significantly greater improvements in empathic accuracy than those receiving placebo at both posttreatment and 1 month follow up. There were no OT-related effects for the other social cognitive tests, clinical symptoms, or neurocognition. This study provides initial support for the idea that OT enhances the effectiveness of training when administered shortly before social cognitive training sessions. The effects were most pronounced on empathic accuracy, a high-level social cognitive process that is not easily improved in current social cognitive remediation programs.</description><identifier>ISSN: 0893-133X</identifier><identifier>EISSN: 1740-634X</identifier><identifier>DOI: 10.1038/npp.2014.68</identifier><identifier>PMID: 24637803</identifier><identifier>CODEN: NEROEW</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>Accuracy ; Administration, Intranasal ; Adult ; Adult and adolescent clinical studies ; Behavior therapy. 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Psychiatry ; Psychoses ; Schizophrenia ; Schizophrenia - therapy ; Schizophrenic Psychology ; Skill development ; Social Perception ; Time Factors ; Treatment Outcome ; Treatments</subject><ispartof>Neuropsychopharmacology (New York, N.Y.), 2014-08, Vol.39 (9), p.2070-2077</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Aug 2014</rights><rights>Copyright © 2014 American College of Neuropsychopharmacology 2014 American College of Neuropsychopharmacology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-2ef30fdc9cb8eac129f592ceb8b949d20764cba109c90a6c6c843d2f02f40e223</citedby><cites>FETCH-LOGICAL-c542t-2ef30fdc9cb8eac129f592ceb8b949d20764cba109c90a6c6c843d2f02f40e223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104336/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104336/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28676303$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24637803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DAVIS, Michael C</creatorcontrib><creatorcontrib>GREEN, Michael F</creatorcontrib><creatorcontrib>JUNGHEE LEE</creatorcontrib><creatorcontrib>HORAN, William P</creatorcontrib><creatorcontrib>SENTURK, Damla</creatorcontrib><creatorcontrib>CLARKE, Angelika D</creatorcontrib><creatorcontrib>MARDER, Stephen R</creatorcontrib><title>Oxytocin-Augmented Social Cognitive Skills Training in Schizophrenia</title><title>Neuropsychopharmacology (New York, N.Y.)</title><addtitle>Neuropsychopharmacology</addtitle><description>Impairments in social cognition are common in schizophrenia and predict poor functional outcome. The purpose of this proof-of-concept randomized, parallel group clinical trial was to assess whether intranasal oxytocin (OT), given before social cognitive training, enhances learning of social cognitive skills. Twenty seven male outpatients with schizophrenia participated in a 6-week (12 session) training on social cognitive skills. Training focused on three domains: facial affect recognition, social perception, and empathy. Subjects were randomly assigned (double blind) to receive either intranasal OTor placebo 30 min before each session. Participants did not receive OT between sessions or on the day of assessments. We evaluated scores on social-cognition measures, as well as clinical symptoms and neurocognition, at baseline, 1 week following the final training session, and 1 month later. Our prespecified primary outcome measure was a social-cognition composite score comprised of five individual measures. There were main effects of time (indicating improvement across the combined-treatment groups) on the social-cognition composite score at both 1 week and 1 month following completion of training. Subjects receiving OT demonstrated significantly greater improvements in empathic accuracy than those receiving placebo at both posttreatment and 1 month follow up. There were no OT-related effects for the other social cognitive tests, clinical symptoms, or neurocognition. This study provides initial support for the idea that OT enhances the effectiveness of training when administered shortly before social cognitive training sessions. The effects were most pronounced on empathic accuracy, a high-level social cognitive process that is not easily improved in current social cognitive remediation programs.</description><subject>Accuracy</subject><subject>Administration, Intranasal</subject><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Behavior therapy. 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Cognitive therapy</topic><topic>Biological and medical sciences</topic><topic>Central Nervous System Agents - administration & dosage</topic><topic>Central Nervous System Agents - adverse effects</topic><topic>Cognition</topic><topic>Cognition & reasoning</topic><topic>Cognitive ability</topic><topic>Cognitive Therapy - methods</topic><topic>Combined Modality Therapy</topic><topic>Double-Blind Method</topic><topic>Drug dosages</topic><topic>Empathy</topic><topic>Facial Expression</topic><topic>Follow-Up Studies</topic><topic>Hormones</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mental disorders</topic><topic>Neuropsychological Tests</topic><topic>Original</topic><topic>Outpatients</topic><topic>Oxytocin - administration & dosage</topic><topic>Oxytocin - adverse effects</topic><topic>Pattern Recognition, Visual</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Schizophrenia</topic><topic>Schizophrenia - therapy</topic><topic>Schizophrenic Psychology</topic><topic>Skill development</topic><topic>Social Perception</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DAVIS, Michael C</creatorcontrib><creatorcontrib>GREEN, Michael F</creatorcontrib><creatorcontrib>JUNGHEE LEE</creatorcontrib><creatorcontrib>HORAN, William P</creatorcontrib><creatorcontrib>SENTURK, Damla</creatorcontrib><creatorcontrib>CLARKE, Angelika D</creatorcontrib><creatorcontrib>MARDER, Stephen R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DAVIS, Michael C</au><au>GREEN, Michael F</au><au>JUNGHEE LEE</au><au>HORAN, William P</au><au>SENTURK, Damla</au><au>CLARKE, Angelika D</au><au>MARDER, Stephen R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxytocin-Augmented Social Cognitive Skills Training in Schizophrenia</atitle><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle><addtitle>Neuropsychopharmacology</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>39</volume><issue>9</issue><spage>2070</spage><epage>2077</epage><pages>2070-2077</pages><issn>0893-133X</issn><eissn>1740-634X</eissn><coden>NEROEW</coden><abstract>Impairments in social cognition are common in schizophrenia and predict poor functional outcome. The purpose of this proof-of-concept randomized, parallel group clinical trial was to assess whether intranasal oxytocin (OT), given before social cognitive training, enhances learning of social cognitive skills. Twenty seven male outpatients with schizophrenia participated in a 6-week (12 session) training on social cognitive skills. Training focused on three domains: facial affect recognition, social perception, and empathy. Subjects were randomly assigned (double blind) to receive either intranasal OTor placebo 30 min before each session. Participants did not receive OT between sessions or on the day of assessments. We evaluated scores on social-cognition measures, as well as clinical symptoms and neurocognition, at baseline, 1 week following the final training session, and 1 month later. Our prespecified primary outcome measure was a social-cognition composite score comprised of five individual measures. There were main effects of time (indicating improvement across the combined-treatment groups) on the social-cognition composite score at both 1 week and 1 month following completion of training. Subjects receiving OT demonstrated significantly greater improvements in empathic accuracy than those receiving placebo at both posttreatment and 1 month follow up. There were no OT-related effects for the other social cognitive tests, clinical symptoms, or neurocognition. This study provides initial support for the idea that OT enhances the effectiveness of training when administered shortly before social cognitive training sessions. The effects were most pronounced on empathic accuracy, a high-level social cognitive process that is not easily improved in current social cognitive remediation programs.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><pmid>24637803</pmid><doi>10.1038/npp.2014.68</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Accuracy Administration, Intranasal Adult Adult and adolescent clinical studies Behavior therapy. Cognitive therapy Biological and medical sciences Central Nervous System Agents - administration & dosage Central Nervous System Agents - adverse effects Cognition Cognition & reasoning Cognitive ability Cognitive Therapy - methods Combined Modality Therapy Double-Blind Method Drug dosages Empathy Facial Expression Follow-Up Studies Hormones Humans Male Medical sciences Mental disorders Neuropsychological Tests Original Outpatients Oxytocin - administration & dosage Oxytocin - adverse effects Pattern Recognition, Visual Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Schizophrenia Schizophrenia - therapy Schizophrenic Psychology Skill development Social Perception Time Factors Treatment Outcome Treatments |
title | Oxytocin-Augmented Social Cognitive Skills Training in Schizophrenia |
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