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Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial

INTRODUCTION: Studies of effective psychotherapy for individuals suffering from the effects of prolonged grief disorder (PGD) are scarce. This paper describes the protocol for an evaluation of a metacognitive therapy programme designed specifically for PGD, to reduce the psychological distress and l...

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Autores principales: Wenn, Jenine, O'Connor, Moira, Breen, Lauren J, Kane, Robert T, Rees, Clare S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4680007/
https://www.ncbi.nlm.nih.gov/pubmed/26646828
http://dx.doi.org/10.1136/bmjopen-2014-007221
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author Wenn, Jenine
O'Connor, Moira
Breen, Lauren J
Kane, Robert T
Rees, Clare S
author_facet Wenn, Jenine
O'Connor, Moira
Breen, Lauren J
Kane, Robert T
Rees, Clare S
author_sort Wenn, Jenine
collection PubMed
description INTRODUCTION: Studies of effective psychotherapy for individuals suffering from the effects of prolonged grief disorder (PGD) are scarce. This paper describes the protocol for an evaluation of a metacognitive therapy programme designed specifically for PGD, to reduce the psychological distress and loss of functioning resulting from bereavement. METHODS AND ANALYSIS: The proposed trial comprises three phases. Phase 1 consists of a review of the literature and semistructured interviews with key members of the target population to inform the development of a metacognitive therapy programme for Prolonged Grief. Phase 2 involves a randomised controlled trial to implement and evaluate the programme. Male and female adults (N=34) will be randomly assigned to either a wait list or an intervention group. Measures of PGD, anxiety, depression, rumination, metacognitions and quality of life will be taken pretreatment and posttreatment and at the 3-month and 6-month follow-up. The generalised linear mixed model will be used to assess treatment efficacy. Phase 3 will test the social validity of the programme. DISCUSSION: This study is the first empirical investigation of the efficacy of a targeted metacognitive treatment programme for PGD. A focus on identifying and changing the metacognitive mechanisms underpinning the development and maintenance of prolonged grief is likely to be beneficial to theory and practice. ETHICS: Ethics approval was obtained from Curtin University Human Research Ethics Committee (Approval number HR 41/2013.) TRIAL REGISTRATION NUMBER: ACTRN12613001270707.
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spelling pubmed-46800072015-12-22 Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial Wenn, Jenine O'Connor, Moira Breen, Lauren J Kane, Robert T Rees, Clare S BMJ Open Mental Health INTRODUCTION: Studies of effective psychotherapy for individuals suffering from the effects of prolonged grief disorder (PGD) are scarce. This paper describes the protocol for an evaluation of a metacognitive therapy programme designed specifically for PGD, to reduce the psychological distress and loss of functioning resulting from bereavement. METHODS AND ANALYSIS: The proposed trial comprises three phases. Phase 1 consists of a review of the literature and semistructured interviews with key members of the target population to inform the development of a metacognitive therapy programme for Prolonged Grief. Phase 2 involves a randomised controlled trial to implement and evaluate the programme. Male and female adults (N=34) will be randomly assigned to either a wait list or an intervention group. Measures of PGD, anxiety, depression, rumination, metacognitions and quality of life will be taken pretreatment and posttreatment and at the 3-month and 6-month follow-up. The generalised linear mixed model will be used to assess treatment efficacy. Phase 3 will test the social validity of the programme. DISCUSSION: This study is the first empirical investigation of the efficacy of a targeted metacognitive treatment programme for PGD. A focus on identifying and changing the metacognitive mechanisms underpinning the development and maintenance of prolonged grief is likely to be beneficial to theory and practice. ETHICS: Ethics approval was obtained from Curtin University Human Research Ethics Committee (Approval number HR 41/2013.) TRIAL REGISTRATION NUMBER: ACTRN12613001270707. BMJ Publishing Group 2015-12-08 /pmc/articles/PMC4680007/ /pubmed/26646828 http://dx.doi.org/10.1136/bmjopen-2014-007221 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Mental Health
Wenn, Jenine
O'Connor, Moira
Breen, Lauren J
Kane, Robert T
Rees, Clare S
Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial
title Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial
title_full Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial
title_fullStr Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial
title_full_unstemmed Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial
title_short Efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial
title_sort efficacy of metacognitive therapy for prolonged grief disorder: protocol for a randomised controlled trial
topic Mental Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4680007/
https://www.ncbi.nlm.nih.gov/pubmed/26646828
http://dx.doi.org/10.1136/bmjopen-2014-007221
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