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A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis
Introduction: There is evidence that early intervention contributes to improving the prognosis and course of first-episode psychosis (FEP). However, further randomised treatment clinical trials are needed. Objectives: The aim of this study was to compare the efficacy of a combined clinical treatment...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304114/ https://www.ncbi.nlm.nih.gov/pubmed/34299697 http://dx.doi.org/10.3390/ijerph18147239 |
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author | González-Ortega, Itxaso Vega, Patricia Echeburúa, Enrique Alberich, Susana Fernández-Sevillano, Jessica Barbeito, Sara Balanzá-Martínez, Vicent Vieta, Eduard Lorente-Rovira, Esther Luengo, Ana Cerrillo, Ester Crespo, José Manuel Matute, Carlos González-Pinto, Ana |
author_facet | González-Ortega, Itxaso Vega, Patricia Echeburúa, Enrique Alberich, Susana Fernández-Sevillano, Jessica Barbeito, Sara Balanzá-Martínez, Vicent Vieta, Eduard Lorente-Rovira, Esther Luengo, Ana Cerrillo, Ester Crespo, José Manuel Matute, Carlos González-Pinto, Ana |
author_sort | González-Ortega, Itxaso |
collection | PubMed |
description | Introduction: There is evidence that early intervention contributes to improving the prognosis and course of first-episode psychosis (FEP). However, further randomised treatment clinical trials are needed. Objectives: The aim of this study was to compare the efficacy of a combined clinical treatment involving Cognitive Behavioural Therapy (CBT) as an adjunctive to treatment-as-usual (TAU) (CBT+TAU) versus TAU alone for FEP. Patients and methods: In this multicentre, single-blind, randomised controlled trial, 177 participants were randomly allocated to either CBT+TAU or TAU. The primary outcome was post-treatment patient functioning. Results: The CBT+TAU group showed a greater improvement in functioning, which was measured using the Global Assessment Functioning (GAF) and Functioning Assessment Short Test (FAST), compared to the TAU group post-treatment. The CBT+TAU participants exhibited a greater decline in depressive, negative, and general psychotic symptoms; a better awareness of the disease and treatment adherence; and a greater increase in brain-derived neurotrophic factor levels than TAU participants. Conclusions: Early intervention based on a combined clinical treatment involving CBT as an adjunctive to standard treatment may improve clinical and functional outcomes in FEP. |
format | Online Article Text |
id | pubmed-8304114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83041142021-07-25 A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis González-Ortega, Itxaso Vega, Patricia Echeburúa, Enrique Alberich, Susana Fernández-Sevillano, Jessica Barbeito, Sara Balanzá-Martínez, Vicent Vieta, Eduard Lorente-Rovira, Esther Luengo, Ana Cerrillo, Ester Crespo, José Manuel Matute, Carlos González-Pinto, Ana Int J Environ Res Public Health Article Introduction: There is evidence that early intervention contributes to improving the prognosis and course of first-episode psychosis (FEP). However, further randomised treatment clinical trials are needed. Objectives: The aim of this study was to compare the efficacy of a combined clinical treatment involving Cognitive Behavioural Therapy (CBT) as an adjunctive to treatment-as-usual (TAU) (CBT+TAU) versus TAU alone for FEP. Patients and methods: In this multicentre, single-blind, randomised controlled trial, 177 participants were randomly allocated to either CBT+TAU or TAU. The primary outcome was post-treatment patient functioning. Results: The CBT+TAU group showed a greater improvement in functioning, which was measured using the Global Assessment Functioning (GAF) and Functioning Assessment Short Test (FAST), compared to the TAU group post-treatment. The CBT+TAU participants exhibited a greater decline in depressive, negative, and general psychotic symptoms; a better awareness of the disease and treatment adherence; and a greater increase in brain-derived neurotrophic factor levels than TAU participants. Conclusions: Early intervention based on a combined clinical treatment involving CBT as an adjunctive to standard treatment may improve clinical and functional outcomes in FEP. MDPI 2021-07-06 /pmc/articles/PMC8304114/ /pubmed/34299697 http://dx.doi.org/10.3390/ijerph18147239 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article González-Ortega, Itxaso Vega, Patricia Echeburúa, Enrique Alberich, Susana Fernández-Sevillano, Jessica Barbeito, Sara Balanzá-Martínez, Vicent Vieta, Eduard Lorente-Rovira, Esther Luengo, Ana Cerrillo, Ester Crespo, José Manuel Matute, Carlos González-Pinto, Ana A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis |
title | A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis |
title_full | A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis |
title_fullStr | A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis |
title_full_unstemmed | A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis |
title_short | A Multicentre, Randomised, Controlled Trial of a Combined Clinical Treatment for First-Episode Psychosis |
title_sort | multicentre, randomised, controlled trial of a combined clinical treatment for first-episode psychosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304114/ https://www.ncbi.nlm.nih.gov/pubmed/34299697 http://dx.doi.org/10.3390/ijerph18147239 |
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