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Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial

Eye movement desensitization and reprocessing (EMDR) is a well-established treatment for post-traumatic stress disorder. Recent research suggested that it may be effective in treating depressive disorders as well. The present study is part of a multicenter randomized-controlled trial, the EDEN study...

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Autores principales: Hase, Michael, Plagge, Jens, Hase, Adrian, Braas, Roger, Ostacoli, Luca, Hofmann, Arne, Huchzermeier, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113947/
https://www.ncbi.nlm.nih.gov/pubmed/30186192
http://dx.doi.org/10.3389/fpsyg.2018.01384
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author Hase, Michael
Plagge, Jens
Hase, Adrian
Braas, Roger
Ostacoli, Luca
Hofmann, Arne
Huchzermeier, Christian
author_facet Hase, Michael
Plagge, Jens
Hase, Adrian
Braas, Roger
Ostacoli, Luca
Hofmann, Arne
Huchzermeier, Christian
author_sort Hase, Michael
collection PubMed
description Eye movement desensitization and reprocessing (EMDR) is a well-established treatment for post-traumatic stress disorder. Recent research suggested that it may be effective in treating depressive disorders as well. The present study is part of a multicenter randomized-controlled trial, the EDEN study, in which a homogenous group of 30 patients was treated to test whether EMDR plus treatment as usual (TAU) would achieve superior results compared to TAU only in a psychosomatic-psychotherapeutic inpatient treatment setting. Both groups were assessed by the Beck Depression Inventory-II (BDI-II) and the Global Severity Index and depression subscale of the Symptom Checklist 90-Revised. The EMDR + TAU group improved significantly better than the TAU group on the BDI-II and Global Severity Index, while a marginally significant difference favoring the EMDR + TAU group over the TAU group was found on the depression subscale. In the EMDR + TAU group, seven out of 14 patients improved below nine points on the BDI-II, which is considered to be a full remission, while four out of 16 in the TAU group did so. These findings confirm earlier suggestions that EMDR therapy may provide additional benefit in the treatment of depression. The present study strengthens the previous literature on EMDR therapy in the treatment of depression due to the randomized-controlled design of the EDEN study.
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spelling pubmed-61139472018-09-05 Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial Hase, Michael Plagge, Jens Hase, Adrian Braas, Roger Ostacoli, Luca Hofmann, Arne Huchzermeier, Christian Front Psychol Psychology Eye movement desensitization and reprocessing (EMDR) is a well-established treatment for post-traumatic stress disorder. Recent research suggested that it may be effective in treating depressive disorders as well. The present study is part of a multicenter randomized-controlled trial, the EDEN study, in which a homogenous group of 30 patients was treated to test whether EMDR plus treatment as usual (TAU) would achieve superior results compared to TAU only in a psychosomatic-psychotherapeutic inpatient treatment setting. Both groups were assessed by the Beck Depression Inventory-II (BDI-II) and the Global Severity Index and depression subscale of the Symptom Checklist 90-Revised. The EMDR + TAU group improved significantly better than the TAU group on the BDI-II and Global Severity Index, while a marginally significant difference favoring the EMDR + TAU group over the TAU group was found on the depression subscale. In the EMDR + TAU group, seven out of 14 patients improved below nine points on the BDI-II, which is considered to be a full remission, while four out of 16 in the TAU group did so. These findings confirm earlier suggestions that EMDR therapy may provide additional benefit in the treatment of depression. The present study strengthens the previous literature on EMDR therapy in the treatment of depression due to the randomized-controlled design of the EDEN study. Frontiers Media S.A. 2018-08-14 /pmc/articles/PMC6113947/ /pubmed/30186192 http://dx.doi.org/10.3389/fpsyg.2018.01384 Text en Copyright © 2018 Hase, Plagge, Hase, Braas, Ostacoli, Hofmann and Huchzermeier. http://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 Psychology
Hase, Michael
Plagge, Jens
Hase, Adrian
Braas, Roger
Ostacoli, Luca
Hofmann, Arne
Huchzermeier, Christian
Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial
title Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial
title_full Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial
title_fullStr Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial
title_full_unstemmed Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial
title_short Eye Movement Desensitization and Reprocessing Versus Treatment as Usual in the Treatment of Depression: A Randomized-Controlled Trial
title_sort eye movement desensitization and reprocessing versus treatment as usual in the treatment of depression: a randomized-controlled trial
topic Psychology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113947/
https://www.ncbi.nlm.nih.gov/pubmed/30186192
http://dx.doi.org/10.3389/fpsyg.2018.01384
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