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MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study

BACKGROUND: Around 150,000 people each year attend hospitals in England due to self-harm, many of them more than once. Over 5,000 people die by suicide each year in the UK, a quarter of them having attended hospital in the previous year because of self-harm. Self-harm is a major identifiable risk fa...

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Autores principales: Collinson, Michelle, Owens, David, Blenkiron, Paul, Burton, Kayleigh, Graham, Liz, Hatcher, Simon, House, Allan, Martin, Katie, Pembroke, Louise, Protheroe, David, Tubeuf, Sandy, Farrin, Amanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020387/
https://www.ncbi.nlm.nih.gov/pubmed/24886683
http://dx.doi.org/10.1186/1745-6215-15-163
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author Collinson, Michelle
Owens, David
Blenkiron, Paul
Burton, Kayleigh
Graham, Liz
Hatcher, Simon
House, Allan
Martin, Katie
Pembroke, Louise
Protheroe, David
Tubeuf, Sandy
Farrin, Amanda
author_facet Collinson, Michelle
Owens, David
Blenkiron, Paul
Burton, Kayleigh
Graham, Liz
Hatcher, Simon
House, Allan
Martin, Katie
Pembroke, Louise
Protheroe, David
Tubeuf, Sandy
Farrin, Amanda
author_sort Collinson, Michelle
collection PubMed
description BACKGROUND: Around 150,000 people each year attend hospitals in England due to self-harm, many of them more than once. Over 5,000 people die by suicide each year in the UK, a quarter of them having attended hospital in the previous year because of self-harm. Self-harm is a major identifiable risk factor for suicide. People receive variable care at hospital; many are not assessed for their psychological needs and little psychological therapy is offered. Despite its frequent occurrence, we have no clear research evidence about how to reduce the repetition of self-harm. Some people who have self-harmed show less active ways of solving problems, and brief problem-solving therapies are considered the most promising psychological treatments. METHODS/DESIGN: This is a pragmatic, individually randomised, controlled, feasibility study comparing interpersonal problem-solving therapy plus treatment-as-usual with treatment-as-usual alone, for adults attending a general hospital following self-harm. A total of 60 participants will be randomised equally between the treatment arms, which will be balanced with respect to the type of most recent self-harm event, number of previous self-harm events, gender and age. Feasibility objectives are as follows: a) To establish and field test procedures for implementing the problem-solving intervention; b) To determine the feasibility and best method of participant recruitment and follow up; c) To assess therapeutic delivery; d) To assess the feasibility of obtaining the definitive trial’s primary and secondary outcomes; e) To assess the perceived burden and acceptability of obtaining the trial’s self-reported outcome data; f) To inform the sample size calculation for the definitive trial. DISCUSSION: The results of this feasibility study will be used to determine the appropriateness of proceeding to a definitive trial and will allow us to design an achievable trial of interpersonal problem-solving therapy for adults who self-harm. TRIAL REGISTRATION: Current Controlled Trials (ISRCTN54036115)
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spelling pubmed-40203872014-05-15 MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study Collinson, Michelle Owens, David Blenkiron, Paul Burton, Kayleigh Graham, Liz Hatcher, Simon House, Allan Martin, Katie Pembroke, Louise Protheroe, David Tubeuf, Sandy Farrin, Amanda Trials Study Protocol BACKGROUND: Around 150,000 people each year attend hospitals in England due to self-harm, many of them more than once. Over 5,000 people die by suicide each year in the UK, a quarter of them having attended hospital in the previous year because of self-harm. Self-harm is a major identifiable risk factor for suicide. People receive variable care at hospital; many are not assessed for their psychological needs and little psychological therapy is offered. Despite its frequent occurrence, we have no clear research evidence about how to reduce the repetition of self-harm. Some people who have self-harmed show less active ways of solving problems, and brief problem-solving therapies are considered the most promising psychological treatments. METHODS/DESIGN: This is a pragmatic, individually randomised, controlled, feasibility study comparing interpersonal problem-solving therapy plus treatment-as-usual with treatment-as-usual alone, for adults attending a general hospital following self-harm. A total of 60 participants will be randomised equally between the treatment arms, which will be balanced with respect to the type of most recent self-harm event, number of previous self-harm events, gender and age. Feasibility objectives are as follows: a) To establish and field test procedures for implementing the problem-solving intervention; b) To determine the feasibility and best method of participant recruitment and follow up; c) To assess therapeutic delivery; d) To assess the feasibility of obtaining the definitive trial’s primary and secondary outcomes; e) To assess the perceived burden and acceptability of obtaining the trial’s self-reported outcome data; f) To inform the sample size calculation for the definitive trial. DISCUSSION: The results of this feasibility study will be used to determine the appropriateness of proceeding to a definitive trial and will allow us to design an achievable trial of interpersonal problem-solving therapy for adults who self-harm. TRIAL REGISTRATION: Current Controlled Trials (ISRCTN54036115) BioMed Central 2014-05-10 /pmc/articles/PMC4020387/ /pubmed/24886683 http://dx.doi.org/10.1186/1745-6215-15-163 Text en Copyright © 2014 Collinson et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 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
Collinson, Michelle
Owens, David
Blenkiron, Paul
Burton, Kayleigh
Graham, Liz
Hatcher, Simon
House, Allan
Martin, Katie
Pembroke, Louise
Protheroe, David
Tubeuf, Sandy
Farrin, Amanda
MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study
title MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study
title_full MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study
title_fullStr MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study
title_full_unstemmed MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study
title_short MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study
title_sort midships: multicentre intervention designed for self-harm using interpersonal problem-solving: protocol for a randomised controlled feasibility study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020387/
https://www.ncbi.nlm.nih.gov/pubmed/24886683
http://dx.doi.org/10.1186/1745-6215-15-163
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