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Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial

Given the relationship between social cognition and functional outcome in schizophrenia, a number of social cognitive interventions have been developed, including Social Cognition Interaction Training (SCIT), a group-based, comprehensive, manualized intervention. In the current trial, we examined SC...

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Autores principales: Fiszdon, Joanna M., Dixon, H. Drew, Davidson, Charlie A., Roberts, David L., Penn, David L., Bell, Morris D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436290/
https://www.ncbi.nlm.nih.gov/pubmed/37599886
http://dx.doi.org/10.3389/fpsyt.2023.1217735
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author Fiszdon, Joanna M.
Dixon, H. Drew
Davidson, Charlie A.
Roberts, David L.
Penn, David L.
Bell, Morris D.
author_facet Fiszdon, Joanna M.
Dixon, H. Drew
Davidson, Charlie A.
Roberts, David L.
Penn, David L.
Bell, Morris D.
author_sort Fiszdon, Joanna M.
collection PubMed
description Given the relationship between social cognition and functional outcome in schizophrenia, a number of social cognitive interventions have been developed, including Social Cognition Interaction Training (SCIT), a group-based, comprehensive, manualized intervention. In the current trial, we examined SCIT efficacy as well as potential moderators of treatment effects. Fifty-one outpatients were randomized to SCIT or a wait-list-control (WLC), with assessments of social cognition, neurocognition, self-report, symptoms, and functioning conducted at baseline and end of the active phase. Relative to WLC, we did not find significant improvements for SCIT on neurocognition, social cognition, self-report, or symptoms, though there was a trend-level, medium effect favoring the SCIT condition on interpersonal and instrumental role function. Post-hoc analyses indicated that baseline neurocognition did not impact degree of social cognitive or functional change. Shorter duration of illness was significantly associated with better post-training neurocognition and self-esteem and, at trend-level with better symptoms and social functioning. We discuss the importance of outcome measure selection and the need for continued evaluation of potential treatment moderators in order to better match people to existing treatments. Clinical trial registration: Clinicaltrials.gov, Identifier NCT00587561.
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spelling pubmed-104362902023-08-19 Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial Fiszdon, Joanna M. Dixon, H. Drew Davidson, Charlie A. Roberts, David L. Penn, David L. Bell, Morris D. Front Psychiatry Psychiatry Given the relationship between social cognition and functional outcome in schizophrenia, a number of social cognitive interventions have been developed, including Social Cognition Interaction Training (SCIT), a group-based, comprehensive, manualized intervention. In the current trial, we examined SCIT efficacy as well as potential moderators of treatment effects. Fifty-one outpatients were randomized to SCIT or a wait-list-control (WLC), with assessments of social cognition, neurocognition, self-report, symptoms, and functioning conducted at baseline and end of the active phase. Relative to WLC, we did not find significant improvements for SCIT on neurocognition, social cognition, self-report, or symptoms, though there was a trend-level, medium effect favoring the SCIT condition on interpersonal and instrumental role function. Post-hoc analyses indicated that baseline neurocognition did not impact degree of social cognitive or functional change. Shorter duration of illness was significantly associated with better post-training neurocognition and self-esteem and, at trend-level with better symptoms and social functioning. We discuss the importance of outcome measure selection and the need for continued evaluation of potential treatment moderators in order to better match people to existing treatments. Clinical trial registration: Clinicaltrials.gov, Identifier NCT00587561. Frontiers Media S.A. 2023-08-04 /pmc/articles/PMC10436290/ /pubmed/37599886 http://dx.doi.org/10.3389/fpsyt.2023.1217735 Text en Copyright © 2023 Fiszdon, Dixon, Davidson, Roberts, Penn and Bell. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Fiszdon, Joanna M.
Dixon, H. Drew
Davidson, Charlie A.
Roberts, David L.
Penn, David L.
Bell, Morris D.
Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial
title Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial
title_full Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial
title_fullStr Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial
title_full_unstemmed Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial
title_short Efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial
title_sort efficacy of social cognition and interaction training in outpatients with schizophrenia spectrum disorders: randomized controlled trial
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436290/
https://www.ncbi.nlm.nih.gov/pubmed/37599886
http://dx.doi.org/10.3389/fpsyt.2023.1217735
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