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Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial
BACKGROUND: With advances in antiretroviral therapy, people with HIV (PWH) are living longer and are less likely to die from AIDS-related complications. Yet, prior research has shown that smoking is often not addressed in the context of HIV care, and few individuals are offered cessation treatment....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636678/ https://www.ncbi.nlm.nih.gov/pubmed/36335376 http://dx.doi.org/10.1186/s13722-022-00341-2 |
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author | Sanford, Brandon T. Toll, Benjamin A. Eckard, Allison Ross Sterba, Katherine R. Cummings, K. Michael Baker, Nathaniel L. Rojewski, Alana M. |
author_facet | Sanford, Brandon T. Toll, Benjamin A. Eckard, Allison Ross Sterba, Katherine R. Cummings, K. Michael Baker, Nathaniel L. Rojewski, Alana M. |
author_sort | Sanford, Brandon T. |
collection | PubMed |
description | BACKGROUND: With advances in antiretroviral therapy, people with HIV (PWH) are living longer and are less likely to die from AIDS-related complications. Yet, prior research has shown that smoking is often not addressed in the context of HIV care, and few individuals are offered cessation treatment. Optimizing tobacco treatment delivery for PWH may increase engagement with evidence-based treatments and successful quit attempts. METHODS: The current study is a type 1 hybrid effectiveness-implementation trial to evaluate the impact of a proactive, opt-out tobacco treatment intervention on cessation outcomes and advance understanding of key barriers and facilitators of implementation processes. A total of 230 PWH who smoke will be recruited from an infectious diseases clinic at an academic medical center and will be randomized to receive (1) treatment as usual (TAU) or (2) Proactive Outreach with Medication Opt-out for Tobacco Treatment Engagement (PrOMOTE). Primary outcomes include: biochemically verified 7-day point prevalence abstinence (PPA) rates, continuous abstinence (Weeks 9–12), and the number of 24-hour quit attempts at the end of study treatment (Week 12). Secondary outcomes include: participant reach (proportion reached out of contact attempts), implementation fidelity (including number of prescriptions written), participant adherence to prescribed pharmacotherapy, acceptability (participant and provider satisfaction with intervention delivery and content), and perceived barriers. DISCUSSION: This study will examine a novel approach to optimizing tobacco treatment delivery for PWH. Integrating effectiveness and implementation results will help define best practices for engaging PWH with evidence-based tobacco treatment interventions. The intervention is low-cost, has the potential to be highly scalable, and could be translatable to other ambulatory HIV clinic settings. TRIAL REGISTRATION: ClinicalTrials.gov: NCT05019495 (August 24, 2021). |
format | Online Article Text |
id | pubmed-9636678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96366782022-11-06 Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial Sanford, Brandon T. Toll, Benjamin A. Eckard, Allison Ross Sterba, Katherine R. Cummings, K. Michael Baker, Nathaniel L. Rojewski, Alana M. Addict Sci Clin Pract Study Protocol BACKGROUND: With advances in antiretroviral therapy, people with HIV (PWH) are living longer and are less likely to die from AIDS-related complications. Yet, prior research has shown that smoking is often not addressed in the context of HIV care, and few individuals are offered cessation treatment. Optimizing tobacco treatment delivery for PWH may increase engagement with evidence-based treatments and successful quit attempts. METHODS: The current study is a type 1 hybrid effectiveness-implementation trial to evaluate the impact of a proactive, opt-out tobacco treatment intervention on cessation outcomes and advance understanding of key barriers and facilitators of implementation processes. A total of 230 PWH who smoke will be recruited from an infectious diseases clinic at an academic medical center and will be randomized to receive (1) treatment as usual (TAU) or (2) Proactive Outreach with Medication Opt-out for Tobacco Treatment Engagement (PrOMOTE). Primary outcomes include: biochemically verified 7-day point prevalence abstinence (PPA) rates, continuous abstinence (Weeks 9–12), and the number of 24-hour quit attempts at the end of study treatment (Week 12). Secondary outcomes include: participant reach (proportion reached out of contact attempts), implementation fidelity (including number of prescriptions written), participant adherence to prescribed pharmacotherapy, acceptability (participant and provider satisfaction with intervention delivery and content), and perceived barriers. DISCUSSION: This study will examine a novel approach to optimizing tobacco treatment delivery for PWH. Integrating effectiveness and implementation results will help define best practices for engaging PWH with evidence-based tobacco treatment interventions. The intervention is low-cost, has the potential to be highly scalable, and could be translatable to other ambulatory HIV clinic settings. TRIAL REGISTRATION: ClinicalTrials.gov: NCT05019495 (August 24, 2021). BioMed Central 2022-11-05 2022 /pmc/articles/PMC9636678/ /pubmed/36335376 http://dx.doi.org/10.1186/s13722-022-00341-2 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 Sanford, Brandon T. Toll, Benjamin A. Eckard, Allison Ross Sterba, Katherine R. Cummings, K. Michael Baker, Nathaniel L. Rojewski, Alana M. Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial |
title | Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial |
title_full | Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial |
title_fullStr | Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial |
title_full_unstemmed | Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial |
title_short | Optimizing tobacco treatment delivery for people with HIV: trial protocol for a randomized controlled trial |
title_sort | optimizing tobacco treatment delivery for people with hiv: trial protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636678/ https://www.ncbi.nlm.nih.gov/pubmed/36335376 http://dx.doi.org/10.1186/s13722-022-00341-2 |
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