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A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial
BACKGROUND: Although existing treatment methods are effective in alleviating PTSD symptoms, several barriers to care exist, such as waiting times, avoidant tendencies, shame and stigma, potentially leading to fewer people seeking therapy or premature dropouts. A potential solution to battling these...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547098/ https://www.ncbi.nlm.nih.gov/pubmed/34696777 http://dx.doi.org/10.1186/s13063-021-05674-y |
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author | Stavland, Halvor Refvik, Camilla Eid, Jarle Lockhat, Rafiq Hammar, Åsa |
author_facet | Stavland, Halvor Refvik, Camilla Eid, Jarle Lockhat, Rafiq Hammar, Åsa |
author_sort | Stavland, Halvor |
collection | PubMed |
description | BACKGROUND: Although existing treatment methods are effective in alleviating PTSD symptoms, several barriers to care exist, such as waiting times, avoidant tendencies, shame and stigma, potentially leading to fewer people seeking therapy or premature dropouts. A potential solution to battling these barriers is Brain Working Recursive Therapy (BWRT), a single-session exposure-oriented intervention for PTSD. Although not yet subjected to empirical investigation, clinical experiences suggest an often immediate and long-lasting effect following the intervention related to patient’s symptomatology and functional abilities. METHODS: The current study protocol outlines a plan to conduct the first non-inferiority randomized controlled trial aimed to explore the efficacy of BWRT compared to treatment as usual (TAU), operationalized as any evidence-based trauma treatment method administered in Norwegian out-patient clinics. Eighty-two participants will be allocated at a 1:1 ratio to one of the following treatment conditions: (1) BWRT or (2) treatment as usual. Participants will be compared on several variables, including changes in PTSD symptoms (primary objective), and changes in perceived quality of life, rumination, functional and cognitive ability (secondary objective). Data collection will take place baseline (T1), within three weeks post treatment (T2) and at 6-month follow-up (T3). DISCUSSION: Should BWRT prove to be non-inferior to treatment as usual, this brief intervention may be an important contribution to future psychological treatment for PTSD, by making trauma treatment more accessible and battling current barriers to care. TRIAL REGISTRATION: 191548, 24.05.2021. ClinicalTrials.gov PRS: Release Confirmation |
format | Online Article Text |
id | pubmed-8547098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85470982021-10-26 A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial Stavland, Halvor Refvik, Camilla Eid, Jarle Lockhat, Rafiq Hammar, Åsa Trials Study Protocol BACKGROUND: Although existing treatment methods are effective in alleviating PTSD symptoms, several barriers to care exist, such as waiting times, avoidant tendencies, shame and stigma, potentially leading to fewer people seeking therapy or premature dropouts. A potential solution to battling these barriers is Brain Working Recursive Therapy (BWRT), a single-session exposure-oriented intervention for PTSD. Although not yet subjected to empirical investigation, clinical experiences suggest an often immediate and long-lasting effect following the intervention related to patient’s symptomatology and functional abilities. METHODS: The current study protocol outlines a plan to conduct the first non-inferiority randomized controlled trial aimed to explore the efficacy of BWRT compared to treatment as usual (TAU), operationalized as any evidence-based trauma treatment method administered in Norwegian out-patient clinics. Eighty-two participants will be allocated at a 1:1 ratio to one of the following treatment conditions: (1) BWRT or (2) treatment as usual. Participants will be compared on several variables, including changes in PTSD symptoms (primary objective), and changes in perceived quality of life, rumination, functional and cognitive ability (secondary objective). Data collection will take place baseline (T1), within three weeks post treatment (T2) and at 6-month follow-up (T3). DISCUSSION: Should BWRT prove to be non-inferior to treatment as usual, this brief intervention may be an important contribution to future psychological treatment for PTSD, by making trauma treatment more accessible and battling current barriers to care. TRIAL REGISTRATION: 191548, 24.05.2021. ClinicalTrials.gov PRS: Release Confirmation BioMed Central 2021-10-25 /pmc/articles/PMC8547098/ /pubmed/34696777 http://dx.doi.org/10.1186/s13063-021-05674-y 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 Stavland, Halvor Refvik, Camilla Eid, Jarle Lockhat, Rafiq Hammar, Åsa A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial |
title | A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial |
title_full | A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial |
title_fullStr | A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial |
title_full_unstemmed | A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial |
title_short | A brief intervention for PTSD versus treatment as usual: Study protocol for a non-inferiority randomized controlled trial |
title_sort | brief intervention for ptsd versus treatment as usual: study protocol for a non-inferiority randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547098/ https://www.ncbi.nlm.nih.gov/pubmed/34696777 http://dx.doi.org/10.1186/s13063-021-05674-y |
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