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Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms

INTRODUCTION: Young people in out-of-home care have often experienced trauma, such as direct maltreatment or witnessing violence. There is good evidence that rates of mental health difficulties are high in this group, including posttraumatic stress disorder (PTSD), a trauma-specific mental health ou...

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Autores principales: Hiller, Rachel M., Davis, Rebecca S., Devaney, John, Halligan, Sarah L., Meiser-Stedman, Richard, Smith, Patrick, Stallard, Paul, Kandiyali, Rebecca, MacNeill, Stephanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590138/
https://www.ncbi.nlm.nih.gov/pubmed/34774093
http://dx.doi.org/10.1186/s40814-021-00936-7
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author Hiller, Rachel M.
Davis, Rebecca S.
Devaney, John
Halligan, Sarah L.
Meiser-Stedman, Richard
Smith, Patrick
Stallard, Paul
Kandiyali, Rebecca
MacNeill, Stephanie
author_facet Hiller, Rachel M.
Davis, Rebecca S.
Devaney, John
Halligan, Sarah L.
Meiser-Stedman, Richard
Smith, Patrick
Stallard, Paul
Kandiyali, Rebecca
MacNeill, Stephanie
author_sort Hiller, Rachel M.
collection PubMed
description INTRODUCTION: Young people in out-of-home care have often experienced trauma, such as direct maltreatment or witnessing violence. There is good evidence that rates of mental health difficulties are high in this group, including posttraumatic stress disorder (PTSD), a trauma-specific mental health outcome. There remains less evidence to guide how to effectively address elevated PTSD symptoms (PTSS) in these young people, particularly in ways that are feasible and scalable for stretched social-care and mental health services. METHODS AND ANALYSIS: This protocol describes a feasibility study comprising a pilot two-arm randomised controlled trial (RCT). Participants (N = 50) will be randomised to either (a) a group-based trauma-focused programme (Teaching Recovery Techniques), delivered by mental health practitioners both online and in-person, or (b) care-as-usual. Primarily, the trial aims to explore the key feasibility and protocol acceptability questions, including rates of recruitment and retention, as well as the acceptability of the intervention (particularly the online delivery format) to participants and services. In addition, outcomes including PTSS (primary clinical outcome), depression and functioning will be assessed at baseline (pre-randomisation), post-intervention and at a 3-month follow-up. ETHICS AND DISSEMINATION: Ethical approval has been received from the Health Research Authority (Wales REC1 Ref 20/WA/0100) and University, with further approval from the host trust and social care site. The results will inform the design of a definitive RCT. Dissemination will include peer-reviewed journal articles reporting the qualitative and quantitative results, as well as presentations at conferences and lay summaries. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04467320. Registered on 13 July 2020.
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spelling pubmed-85901382021-11-15 Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms Hiller, Rachel M. Davis, Rebecca S. Devaney, John Halligan, Sarah L. Meiser-Stedman, Richard Smith, Patrick Stallard, Paul Kandiyali, Rebecca MacNeill, Stephanie Pilot Feasibility Stud Study Protocol INTRODUCTION: Young people in out-of-home care have often experienced trauma, such as direct maltreatment or witnessing violence. There is good evidence that rates of mental health difficulties are high in this group, including posttraumatic stress disorder (PTSD), a trauma-specific mental health outcome. There remains less evidence to guide how to effectively address elevated PTSD symptoms (PTSS) in these young people, particularly in ways that are feasible and scalable for stretched social-care and mental health services. METHODS AND ANALYSIS: This protocol describes a feasibility study comprising a pilot two-arm randomised controlled trial (RCT). Participants (N = 50) will be randomised to either (a) a group-based trauma-focused programme (Teaching Recovery Techniques), delivered by mental health practitioners both online and in-person, or (b) care-as-usual. Primarily, the trial aims to explore the key feasibility and protocol acceptability questions, including rates of recruitment and retention, as well as the acceptability of the intervention (particularly the online delivery format) to participants and services. In addition, outcomes including PTSS (primary clinical outcome), depression and functioning will be assessed at baseline (pre-randomisation), post-intervention and at a 3-month follow-up. ETHICS AND DISSEMINATION: Ethical approval has been received from the Health Research Authority (Wales REC1 Ref 20/WA/0100) and University, with further approval from the host trust and social care site. The results will inform the design of a definitive RCT. Dissemination will include peer-reviewed journal articles reporting the qualitative and quantitative results, as well as presentations at conferences and lay summaries. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04467320. Registered on 13 July 2020. BioMed Central 2021-11-13 /pmc/articles/PMC8590138/ /pubmed/34774093 http://dx.doi.org/10.1186/s40814-021-00936-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Hiller, Rachel M.
Davis, Rebecca S.
Devaney, John
Halligan, Sarah L.
Meiser-Stedman, Richard
Smith, Patrick
Stallard, Paul
Kandiyali, Rebecca
MacNeill, Stephanie
Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms
title Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms
title_full Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms
title_fullStr Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms
title_full_unstemmed Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms
title_short Protocol for the RELATE trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms
title_sort protocol for the relate trial: a feasibility and pilot randomised controlled trial of a low-intensity group intervention for young people in care with elevated posttraumatic stress symptoms
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590138/
https://www.ncbi.nlm.nih.gov/pubmed/34774093
http://dx.doi.org/10.1186/s40814-021-00936-7
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