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Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial

BACKGROUND: Depressive disorders are highly prevalent in primary care (PC) and are associated with considerable functional impairment and increased health care use. Research has shown that many patients prefer psychological treatments to pharmacotherapy, however, it remains unclear which treatment i...

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Autores principales: Baas, Kim D, Koeter, Maarten WJ, van Weert, Henk C, Lucassen, Peter, Bockting, Claudi LH, Wittkampf, Karin A, Schene, Aart H
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964697/
https://www.ncbi.nlm.nih.gov/pubmed/20939917
http://dx.doi.org/10.1186/1745-6215-11-96
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author Baas, Kim D
Koeter, Maarten WJ
van Weert, Henk C
Lucassen, Peter
Bockting, Claudi LH
Wittkampf, Karin A
Schene, Aart H
author_facet Baas, Kim D
Koeter, Maarten WJ
van Weert, Henk C
Lucassen, Peter
Bockting, Claudi LH
Wittkampf, Karin A
Schene, Aart H
author_sort Baas, Kim D
collection PubMed
description BACKGROUND: Depressive disorders are highly prevalent in primary care (PC) and are associated with considerable functional impairment and increased health care use. Research has shown that many patients prefer psychological treatments to pharmacotherapy, however, it remains unclear which treatment is most optimal for depressive patients in primary care. METHODS/DESIGN: A randomized, multi-centre trial involving two intervention groups: one receiving brief cognitive behavioral therapy and the other receiving general practitioner care. General practitioners from 109 General Practices in Nijmegen and Amsterdam (The Netherlands) will be asked to include patients aged between 18-70 years presenting with depressive symptomatology, who do not receive an active treatment for their depressive complaints. Patients will be telephonically assessed with the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-I) to ascertain study eligibility. Eligible patients will be randomized to one of two treatment conditions: either 8 sessions of cognitive behavioral therapy by a first line psychologist or general practitioner's care according to The Dutch College of General Practitioners Practice Guideline (NHG- standaard). Baseline and follow-up assessments are scheduled at 0, 6, 12 and 52 weeks following the start of the intervention. Primary outcome will be measured with the Hamilton Depression Rating Scale-17 (HDRS-17) and the Patient Health Questionnaire-9 (PHQ-9). Outcomes will be analyzed on an intention to treat basis. TRIAL REGISTRATION: ISRCTN65811640
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spelling pubmed-29646972010-10-28 Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial Baas, Kim D Koeter, Maarten WJ van Weert, Henk C Lucassen, Peter Bockting, Claudi LH Wittkampf, Karin A Schene, Aart H Trials Study Protocol BACKGROUND: Depressive disorders are highly prevalent in primary care (PC) and are associated with considerable functional impairment and increased health care use. Research has shown that many patients prefer psychological treatments to pharmacotherapy, however, it remains unclear which treatment is most optimal for depressive patients in primary care. METHODS/DESIGN: A randomized, multi-centre trial involving two intervention groups: one receiving brief cognitive behavioral therapy and the other receiving general practitioner care. General practitioners from 109 General Practices in Nijmegen and Amsterdam (The Netherlands) will be asked to include patients aged between 18-70 years presenting with depressive symptomatology, who do not receive an active treatment for their depressive complaints. Patients will be telephonically assessed with the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-I) to ascertain study eligibility. Eligible patients will be randomized to one of two treatment conditions: either 8 sessions of cognitive behavioral therapy by a first line psychologist or general practitioner's care according to The Dutch College of General Practitioners Practice Guideline (NHG- standaard). Baseline and follow-up assessments are scheduled at 0, 6, 12 and 52 weeks following the start of the intervention. Primary outcome will be measured with the Hamilton Depression Rating Scale-17 (HDRS-17) and the Patient Health Questionnaire-9 (PHQ-9). Outcomes will be analyzed on an intention to treat basis. TRIAL REGISTRATION: ISRCTN65811640 BioMed Central 2010-10-12 /pmc/articles/PMC2964697/ /pubmed/20939917 http://dx.doi.org/10.1186/1745-6215-11-96 Text en Copyright ©2010 Baas et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Baas, Kim D
Koeter, Maarten WJ
van Weert, Henk C
Lucassen, Peter
Bockting, Claudi LH
Wittkampf, Karin A
Schene, Aart H
Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial
title Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial
title_full Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial
title_fullStr Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial
title_full_unstemmed Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial
title_short Brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial
title_sort brief cognitive behavioral therapy compared to general practitioners care for depression in primary care: a randomized trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964697/
https://www.ncbi.nlm.nih.gov/pubmed/20939917
http://dx.doi.org/10.1186/1745-6215-11-96
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