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A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia

BACKGROUND: Depression is highly prevalent within individuals diagnosed with schizophrenia, and is associated with an increased risk of suicide. There are no current evidence based treatments for low mood within this group. The specific targeting of co-morbid conditions within complex mental health...

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Autores principales: Steel, Craig, van der Gaag, Mark, Korrelboom, Kees, Simon, Judit, Phiri, Peter, Baksh, M Fazil, Wykes, Til, Rose, Diana, Rose, Suzanna, Hardcastle, Mark, Enright, Simon, Evans, Gareth, Kingdon, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414283/
https://www.ncbi.nlm.nih.gov/pubmed/25886265
http://dx.doi.org/10.1186/s12888-015-0453-6
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author Steel, Craig
van der Gaag, Mark
Korrelboom, Kees
Simon, Judit
Phiri, Peter
Baksh, M Fazil
Wykes, Til
Rose, Diana
Rose, Suzanna
Hardcastle, Mark
Enright, Simon
Evans, Gareth
Kingdon, David
author_facet Steel, Craig
van der Gaag, Mark
Korrelboom, Kees
Simon, Judit
Phiri, Peter
Baksh, M Fazil
Wykes, Til
Rose, Diana
Rose, Suzanna
Hardcastle, Mark
Enright, Simon
Evans, Gareth
Kingdon, David
author_sort Steel, Craig
collection PubMed
description BACKGROUND: Depression is highly prevalent within individuals diagnosed with schizophrenia, and is associated with an increased risk of suicide. There are no current evidence based treatments for low mood within this group. The specific targeting of co-morbid conditions within complex mental health problems lends itself to the development of short-term structured interventions which are relatively easy to disseminate within health services. A brief cognitive intervention based on a competitive memory theory of depression, is being evaluated in terms of its effectiveness in reducing depression within this group. METHODS/DESIGN: This is a single blind, intention-to-treat, multi-site, randomized controlled trial comparing Positive Memory Training plus Treatment as Usual with Treatment as Usual alone. Participants will be recruited from two NHS Trusts in Southern England. In order to be eligible, participants must have a DSM-V diagnosis of schizophrenia or schizo-affective disorder and exhibit at least a mild level of depression. Following baseline assessment eligible participants will be randomly allocated to either the Positive Memory Training plus Treatment as Usual group or the Treatment as Usual group. Outcome will be assessed at the end of treatment (3-months) and at 6-month and 9-month post randomization by assessors blind to group allocation. The primary outcome will be levels of depression and secondary outcomes will be severity of psychotic symptoms and cost-effectiveness. Semi-structured interviews will be conducted with all participants who are allocated to the treatment group so as to explore the acceptability of the intervention. DISCUSSION: Cognitive behaviour therapy is recommended for individuals diagnosed with schizophrenia. However, the number of sessions and length of training required to deliver this intervention has caused a limit in availability. The current trial will evaluate a short-term structured protocol which targets a co-morbid condition often considered of primary importance by service users. If successful the intervention will be an important addition to current initiatives aimed at increasing access to psychological therapies for people diagnosed with severe mental health problems. TRIAL REGISTRATION: Current Controlled Trials. ISRCTN99485756. Registered 13 March 2014.
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spelling pubmed-44142832015-04-30 A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia Steel, Craig van der Gaag, Mark Korrelboom, Kees Simon, Judit Phiri, Peter Baksh, M Fazil Wykes, Til Rose, Diana Rose, Suzanna Hardcastle, Mark Enright, Simon Evans, Gareth Kingdon, David BMC Psychiatry Study Protocol BACKGROUND: Depression is highly prevalent within individuals diagnosed with schizophrenia, and is associated with an increased risk of suicide. There are no current evidence based treatments for low mood within this group. The specific targeting of co-morbid conditions within complex mental health problems lends itself to the development of short-term structured interventions which are relatively easy to disseminate within health services. A brief cognitive intervention based on a competitive memory theory of depression, is being evaluated in terms of its effectiveness in reducing depression within this group. METHODS/DESIGN: This is a single blind, intention-to-treat, multi-site, randomized controlled trial comparing Positive Memory Training plus Treatment as Usual with Treatment as Usual alone. Participants will be recruited from two NHS Trusts in Southern England. In order to be eligible, participants must have a DSM-V diagnosis of schizophrenia or schizo-affective disorder and exhibit at least a mild level of depression. Following baseline assessment eligible participants will be randomly allocated to either the Positive Memory Training plus Treatment as Usual group or the Treatment as Usual group. Outcome will be assessed at the end of treatment (3-months) and at 6-month and 9-month post randomization by assessors blind to group allocation. The primary outcome will be levels of depression and secondary outcomes will be severity of psychotic symptoms and cost-effectiveness. Semi-structured interviews will be conducted with all participants who are allocated to the treatment group so as to explore the acceptability of the intervention. DISCUSSION: Cognitive behaviour therapy is recommended for individuals diagnosed with schizophrenia. However, the number of sessions and length of training required to deliver this intervention has caused a limit in availability. The current trial will evaluate a short-term structured protocol which targets a co-morbid condition often considered of primary importance by service users. If successful the intervention will be an important addition to current initiatives aimed at increasing access to psychological therapies for people diagnosed with severe mental health problems. TRIAL REGISTRATION: Current Controlled Trials. ISRCTN99485756. Registered 13 March 2014. BioMed Central 2015-04-14 /pmc/articles/PMC4414283/ /pubmed/25886265 http://dx.doi.org/10.1186/s12888-015-0453-6 Text en © Steel et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Steel, Craig
van der Gaag, Mark
Korrelboom, Kees
Simon, Judit
Phiri, Peter
Baksh, M Fazil
Wykes, Til
Rose, Diana
Rose, Suzanna
Hardcastle, Mark
Enright, Simon
Evans, Gareth
Kingdon, David
A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia
title A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia
title_full A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia
title_fullStr A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia
title_full_unstemmed A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia
title_short A randomised controlled trial of positive memory training for the treatment of depression within schizophrenia
title_sort randomised controlled trial of positive memory training for the treatment of depression within schizophrenia
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414283/
https://www.ncbi.nlm.nih.gov/pubmed/25886265
http://dx.doi.org/10.1186/s12888-015-0453-6
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