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A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up
This paper reports the 1-year follow-up results from a randomized controlled trial (RCT), which examined the efficacy of metacognitive therapy (MCT) for unipolar depression compared to a waiting condition. Thirty-nine patients with major depression were offered MCT and were divided into two conditio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694776/ https://www.ncbi.nlm.nih.gov/pubmed/31440193 http://dx.doi.org/10.3389/fpsyg.2019.01842 |
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author | Hjemdal, Odin Solem, Stian Hagen, Roger Kennair, Leif Edward Ottesen Nordahl, Hans M. Wells, Adrian |
author_facet | Hjemdal, Odin Solem, Stian Hagen, Roger Kennair, Leif Edward Ottesen Nordahl, Hans M. Wells, Adrian |
author_sort | Hjemdal, Odin |
collection | PubMed |
description | This paper reports the 1-year follow-up results from a randomized controlled trial (RCT), which examined the efficacy of metacognitive therapy (MCT) for unipolar depression compared to a waiting condition. Thirty-nine patients with major depression were offered MCT and were divided into two conditions; immediate MCT with 10 weekly sessions or a waiting period that had a 10-week delayed MCT start. Two participants dropped out during the waiting condition. Thirty-four patients participated in the follow-up assessment. Based on the intent-to-treat sample and all patients, 67% were classified as recovered, 13% improved, and 20% were unchanged at 1-year follow-up. For the completers sample 73% recovered, 12% improved, and 15% were unchanged. Five of the 31 patients (13%) that were in remission at post-treatment experienced relapse at 1-year follow-up. Within-group effect sizes were large for reductions in symptoms of depression (d = 2.09) and anxiety (d = 1.16) at 1-year. Treatment response was associated with reductions in rumination, worry, and metacognitive beliefs as predicted by the metacognitive model, but reductions in metacognitions independently predicted reductions in depression scores from pre-treatment to 1-year follow-up. The results suggest that treatment gains are stable at 1-year follow-up. The study sets the stage for future research, which should evaluate MCT over a longer term and compare it with active treatments using suitably powered RCTs. |
format | Online Article Text |
id | pubmed-6694776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66947762019-08-22 A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up Hjemdal, Odin Solem, Stian Hagen, Roger Kennair, Leif Edward Ottesen Nordahl, Hans M. Wells, Adrian Front Psychol Psychology This paper reports the 1-year follow-up results from a randomized controlled trial (RCT), which examined the efficacy of metacognitive therapy (MCT) for unipolar depression compared to a waiting condition. Thirty-nine patients with major depression were offered MCT and were divided into two conditions; immediate MCT with 10 weekly sessions or a waiting period that had a 10-week delayed MCT start. Two participants dropped out during the waiting condition. Thirty-four patients participated in the follow-up assessment. Based on the intent-to-treat sample and all patients, 67% were classified as recovered, 13% improved, and 20% were unchanged at 1-year follow-up. For the completers sample 73% recovered, 12% improved, and 15% were unchanged. Five of the 31 patients (13%) that were in remission at post-treatment experienced relapse at 1-year follow-up. Within-group effect sizes were large for reductions in symptoms of depression (d = 2.09) and anxiety (d = 1.16) at 1-year. Treatment response was associated with reductions in rumination, worry, and metacognitive beliefs as predicted by the metacognitive model, but reductions in metacognitions independently predicted reductions in depression scores from pre-treatment to 1-year follow-up. The results suggest that treatment gains are stable at 1-year follow-up. The study sets the stage for future research, which should evaluate MCT over a longer term and compare it with active treatments using suitably powered RCTs. Frontiers Media S.A. 2019-08-08 /pmc/articles/PMC6694776/ /pubmed/31440193 http://dx.doi.org/10.3389/fpsyg.2019.01842 Text en Copyright © 2019 Hjemdal, Solem, Hagen, Kennair, Nordahl and Wells. 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 Hjemdal, Odin Solem, Stian Hagen, Roger Kennair, Leif Edward Ottesen Nordahl, Hans M. Wells, Adrian A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up |
title | A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up |
title_full | A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up |
title_fullStr | A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up |
title_full_unstemmed | A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up |
title_short | A Randomized Controlled Trial of Metacognitive Therapy for Depression: Analysis of 1-Year Follow-Up |
title_sort | randomized controlled trial of metacognitive therapy for depression: analysis of 1-year follow-up |
topic | Psychology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694776/ https://www.ncbi.nlm.nih.gov/pubmed/31440193 http://dx.doi.org/10.3389/fpsyg.2019.01842 |
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