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Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care

BACKGROUND: The US continues to face public health crises related to both chronic pain and opioid overdoses. Thirty percent of Americans suffer from chronic noncancer pain at an estimated yearly cost of over $600 billion. Most patients with chronic pain turn to primary care clinicians who must choos...

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Autores principales: Salloum, Ramzi G., Bilello, Lori, Bian, Jiang, Diiulio, Julie, Paz, Laura Gonzalez, Gurka, Matthew J., Gutierrez, Maria, Hurley, Robert W., Jones, Ross E., Martinez-Wittinghan, Francisco, Marcial, Laura, Masri, Ghania, McDonnell, Cara, Militello, Laura G., Modave, François, Nguyen, Khoa, Rhodes, Bryn, Siler, Kendra, Willis, David, Harle, Christopher A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287973/
https://www.ncbi.nlm.nih.gov/pubmed/35841043
http://dx.doi.org/10.1186/s13012-022-01217-4
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author Salloum, Ramzi G.
Bilello, Lori
Bian, Jiang
Diiulio, Julie
Paz, Laura Gonzalez
Gurka, Matthew J.
Gutierrez, Maria
Hurley, Robert W.
Jones, Ross E.
Martinez-Wittinghan, Francisco
Marcial, Laura
Masri, Ghania
McDonnell, Cara
Militello, Laura G.
Modave, François
Nguyen, Khoa
Rhodes, Bryn
Siler, Kendra
Willis, David
Harle, Christopher A.
author_facet Salloum, Ramzi G.
Bilello, Lori
Bian, Jiang
Diiulio, Julie
Paz, Laura Gonzalez
Gurka, Matthew J.
Gutierrez, Maria
Hurley, Robert W.
Jones, Ross E.
Martinez-Wittinghan, Francisco
Marcial, Laura
Masri, Ghania
McDonnell, Cara
Militello, Laura G.
Modave, François
Nguyen, Khoa
Rhodes, Bryn
Siler, Kendra
Willis, David
Harle, Christopher A.
author_sort Salloum, Ramzi G.
collection PubMed
description BACKGROUND: The US continues to face public health crises related to both chronic pain and opioid overdoses. Thirty percent of Americans suffer from chronic noncancer pain at an estimated yearly cost of over $600 billion. Most patients with chronic pain turn to primary care clinicians who must choose from myriad treatment options based on relative risks and benefits, patient history, available resources, symptoms, and goals. Recently, with attention to opioid-related risks, prescribing has declined. However, clinical experts have countered with concerns that some patients for whom opioid-related benefits outweigh risks may be inappropriately discontinued from opioids. Unfortunately, primary care clinicians lack usable tools to help them partner with their patients in choosing pain treatment options that best balance risks and benefits in the context of patient history, resources, symptoms, and goals. Thus, primary care clinicians and patients would benefit from patient-centered clinical decision support (CDS) for this shared decision-making process. METHODS: The objective of this 3-year project is to study the adaptation and implementation of an existing interoperable CDS tool for pain treatment shared decision making, with tailored implementation support, in new clinical settings in the OneFlorida Clinical Research Consortium. Our central hypothesis is that tailored implementation support will increase CDS adoption and shared decision making. We further hypothesize that increases in shared decision making will lead to improved patient outcomes, specifically pain and physical function. The CDS implementation will be guided by the Exploration, Preparation, Implementation, Sustainment (EPIS) framework. The evaluation will be organized by the Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) framework. We will adapt and tailor PainManager, an open source interoperable CDS tool, for implementation in primary care clinics affiliated with the OneFlorida Clinical Research Consortium. We will evaluate the effect of tailored implementation support on PainManager’s adoption for pain treatment shared decision making. This evaluation will establish the feasibility and obtain preliminary data in preparation for a multi-site pragmatic trial targeting the effectiveness of PainManager and tailored implementation support on shared decision making and patient-reported pain and physical function. DISCUSSION: This research will generate evidence on strategies for implementing interoperable CDS in new clinical settings across different types of electronic health records (EHRs). The study will also inform tailored implementation strategies to be further tested in a subsequent hybrid effectiveness-implementation trial. Together, these efforts will lead to important new technology and evidence that patients, clinicians, and health systems can use to improve care for millions of Americans who suffer from pain and other chronic conditions. TRIAL REGISTRATION: ClinicalTrials.gov, NCT05256394, Registered 25 February 2022. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13012-022-01217-4.
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spelling pubmed-92879732022-07-17 Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care Salloum, Ramzi G. Bilello, Lori Bian, Jiang Diiulio, Julie Paz, Laura Gonzalez Gurka, Matthew J. Gutierrez, Maria Hurley, Robert W. Jones, Ross E. Martinez-Wittinghan, Francisco Marcial, Laura Masri, Ghania McDonnell, Cara Militello, Laura G. Modave, François Nguyen, Khoa Rhodes, Bryn Siler, Kendra Willis, David Harle, Christopher A. Implement Sci Study Protocol BACKGROUND: The US continues to face public health crises related to both chronic pain and opioid overdoses. Thirty percent of Americans suffer from chronic noncancer pain at an estimated yearly cost of over $600 billion. Most patients with chronic pain turn to primary care clinicians who must choose from myriad treatment options based on relative risks and benefits, patient history, available resources, symptoms, and goals. Recently, with attention to opioid-related risks, prescribing has declined. However, clinical experts have countered with concerns that some patients for whom opioid-related benefits outweigh risks may be inappropriately discontinued from opioids. Unfortunately, primary care clinicians lack usable tools to help them partner with their patients in choosing pain treatment options that best balance risks and benefits in the context of patient history, resources, symptoms, and goals. Thus, primary care clinicians and patients would benefit from patient-centered clinical decision support (CDS) for this shared decision-making process. METHODS: The objective of this 3-year project is to study the adaptation and implementation of an existing interoperable CDS tool for pain treatment shared decision making, with tailored implementation support, in new clinical settings in the OneFlorida Clinical Research Consortium. Our central hypothesis is that tailored implementation support will increase CDS adoption and shared decision making. We further hypothesize that increases in shared decision making will lead to improved patient outcomes, specifically pain and physical function. The CDS implementation will be guided by the Exploration, Preparation, Implementation, Sustainment (EPIS) framework. The evaluation will be organized by the Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) framework. We will adapt and tailor PainManager, an open source interoperable CDS tool, for implementation in primary care clinics affiliated with the OneFlorida Clinical Research Consortium. We will evaluate the effect of tailored implementation support on PainManager’s adoption for pain treatment shared decision making. This evaluation will establish the feasibility and obtain preliminary data in preparation for a multi-site pragmatic trial targeting the effectiveness of PainManager and tailored implementation support on shared decision making and patient-reported pain and physical function. DISCUSSION: This research will generate evidence on strategies for implementing interoperable CDS in new clinical settings across different types of electronic health records (EHRs). The study will also inform tailored implementation strategies to be further tested in a subsequent hybrid effectiveness-implementation trial. Together, these efforts will lead to important new technology and evidence that patients, clinicians, and health systems can use to improve care for millions of Americans who suffer from pain and other chronic conditions. TRIAL REGISTRATION: ClinicalTrials.gov, NCT05256394, Registered 25 February 2022. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13012-022-01217-4. BioMed Central 2022-07-15 /pmc/articles/PMC9287973/ /pubmed/35841043 http://dx.doi.org/10.1186/s13012-022-01217-4 Text en © The Author(s) 2022 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
Salloum, Ramzi G.
Bilello, Lori
Bian, Jiang
Diiulio, Julie
Paz, Laura Gonzalez
Gurka, Matthew J.
Gutierrez, Maria
Hurley, Robert W.
Jones, Ross E.
Martinez-Wittinghan, Francisco
Marcial, Laura
Masri, Ghania
McDonnell, Cara
Militello, Laura G.
Modave, François
Nguyen, Khoa
Rhodes, Bryn
Siler, Kendra
Willis, David
Harle, Christopher A.
Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care
title Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care
title_full Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care
title_fullStr Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care
title_full_unstemmed Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care
title_short Study protocol for a type III hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care
title_sort study protocol for a type iii hybrid effectiveness-implementation trial to evaluate scaling interoperable clinical decision support for patient-centered chronic pain management in primary care
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287973/
https://www.ncbi.nlm.nih.gov/pubmed/35841043
http://dx.doi.org/10.1186/s13012-022-01217-4
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