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Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research
BACKGROUND: This manuscript provides a research update to the ongoing pragmatic trial of Project POINT (Planned Outreach, Intervention, Naloxone, and Treatment), an emergency department-based peer recovery coaching intervention for linking patients with opioid use disorder to evidence-based treatmen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859893/ https://www.ncbi.nlm.nih.gov/pubmed/33541402 http://dx.doi.org/10.1186/s13063-021-05065-3 |
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author | Dir, Allyson L. Watson, Dennis P. Zhiss, Matthew Taylor, Lisa Bray, Bethany C. McGuire, Alan |
author_facet | Dir, Allyson L. Watson, Dennis P. Zhiss, Matthew Taylor, Lisa Bray, Bethany C. McGuire, Alan |
author_sort | Dir, Allyson L. |
collection | PubMed |
description | BACKGROUND: This manuscript provides a research update to the ongoing pragmatic trial of Project POINT (Planned Outreach, Intervention, Naloxone, and Treatment), an emergency department-based peer recovery coaching intervention for linking patients with opioid use disorder to evidence-based treatment. The research team has encountered a number of challenges related to the “real-world” study setting since the trial began. Using an implementation science lens, we sought to identify and describe barriers impacting both the intervention and research protocols of the POINT study, which are often intertwined in pragmatic trials due to the focus on external validity. METHOD: Qualitative data were collected from 3 peer recovery coaches, 2 peer recovery coach supervisors, and 3 members of the research team. Questions and deductive qualitative analysis were guided by the Consolidated Framework for Implementation Research (CFIR). RESULTS: Nine unique barriers were noted, with 5 of these barriers impacting intervention and research protocol implementation simultaneously. These simultaneous barriers were timing of intervention delivery, ineffective communication with emergency department staff, lack of privacy in the emergency department, the fast-paced emergency department setting, and patient’s limited resources. Together, these barriers represent the intervention characteristics, inner setting, and outer setting domains of the CFIR. CONCLUSION: Results highlight the utility of employing an implementation science framework to assess implementation issues in pragmatic trials and how this approach might be used as a quality assurance mechanism given the considerable overlap that exists between research and intervention protocols in real-world trial settings. Previously undocumented changes to the trial design that have been made as a result of the identified barriers are discussed. |
format | Online Article Text |
id | pubmed-7859893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78598932021-02-04 Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research Dir, Allyson L. Watson, Dennis P. Zhiss, Matthew Taylor, Lisa Bray, Bethany C. McGuire, Alan Trials Update BACKGROUND: This manuscript provides a research update to the ongoing pragmatic trial of Project POINT (Planned Outreach, Intervention, Naloxone, and Treatment), an emergency department-based peer recovery coaching intervention for linking patients with opioid use disorder to evidence-based treatment. The research team has encountered a number of challenges related to the “real-world” study setting since the trial began. Using an implementation science lens, we sought to identify and describe barriers impacting both the intervention and research protocols of the POINT study, which are often intertwined in pragmatic trials due to the focus on external validity. METHOD: Qualitative data were collected from 3 peer recovery coaches, 2 peer recovery coach supervisors, and 3 members of the research team. Questions and deductive qualitative analysis were guided by the Consolidated Framework for Implementation Research (CFIR). RESULTS: Nine unique barriers were noted, with 5 of these barriers impacting intervention and research protocol implementation simultaneously. These simultaneous barriers were timing of intervention delivery, ineffective communication with emergency department staff, lack of privacy in the emergency department, the fast-paced emergency department setting, and patient’s limited resources. Together, these barriers represent the intervention characteristics, inner setting, and outer setting domains of the CFIR. CONCLUSION: Results highlight the utility of employing an implementation science framework to assess implementation issues in pragmatic trials and how this approach might be used as a quality assurance mechanism given the considerable overlap that exists between research and intervention protocols in real-world trial settings. Previously undocumented changes to the trial design that have been made as a result of the identified barriers are discussed. BioMed Central 2021-02-04 /pmc/articles/PMC7859893/ /pubmed/33541402 http://dx.doi.org/10.1186/s13063-021-05065-3 Text en © The Author(s) 2021 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/. 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 in a credit line to the data. |
spellingShingle | Update Dir, Allyson L. Watson, Dennis P. Zhiss, Matthew Taylor, Lisa Bray, Bethany C. McGuire, Alan Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research |
title | Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research |
title_full | Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research |
title_fullStr | Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research |
title_full_unstemmed | Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research |
title_short | Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research |
title_sort | barriers impacting the point pragmatic trial: the unavoidable overlap between research and intervention procedures in “real-world” research |
topic | Update |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859893/ https://www.ncbi.nlm.nih.gov/pubmed/33541402 http://dx.doi.org/10.1186/s13063-021-05065-3 |
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