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‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention

INTRODUCTION: A key contributor to underimmunisation is parental refusal or delay of vaccines due to vaccine concerns. Many clinicians lack confidence in communicating with vaccine-hesitant parents (VHP) and perceive that their discussions will do little to change parents’ minds. Improving clinician...

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Autores principales: Opel, Douglas J, Robinson, Jeffrey D, Spielvogle, Heather, Spina, Christine, Garrett, Kathleen, Dempsey, Amanda F, Perreira, Cathryn, Dickinson, Miriam, Zhou, Chuan, Pahud, Barbara, Taylor, James A, O'Leary, Sean T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418671/
https://www.ncbi.nlm.nih.gov/pubmed/32784263
http://dx.doi.org/10.1136/bmjopen-2020-039299
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author Opel, Douglas J
Robinson, Jeffrey D
Spielvogle, Heather
Spina, Christine
Garrett, Kathleen
Dempsey, Amanda F
Perreira, Cathryn
Dickinson, Miriam
Zhou, Chuan
Pahud, Barbara
Taylor, James A
O'Leary, Sean T
author_facet Opel, Douglas J
Robinson, Jeffrey D
Spielvogle, Heather
Spina, Christine
Garrett, Kathleen
Dempsey, Amanda F
Perreira, Cathryn
Dickinson, Miriam
Zhou, Chuan
Pahud, Barbara
Taylor, James A
O'Leary, Sean T
author_sort Opel, Douglas J
collection PubMed
description INTRODUCTION: A key contributor to underimmunisation is parental refusal or delay of vaccines due to vaccine concerns. Many clinicians lack confidence in communicating with vaccine-hesitant parents (VHP) and perceive that their discussions will do little to change parents’ minds. Improving clinician communication with VHPs is critical to increasing childhood vaccine uptake. METHODS AND ANALYSIS: We describe the protocol for a cluster randomised controlled trial to test the impact of a novel, multifaceted clinician vaccine communication strategy on child immunisation status. The trial will be conducted in 24 primary care practices in two US states (Washington and Colorado). The strategy is called Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing (PIVOT with MI), and involves clinicians initiating the vaccine conversation with all parents of young children using the presumptive format, and among those parents who resist vaccines, pivoting to using MI. Our primary outcome is the immunisation status of children of VHPs at 19 months, 0 day of age expressed as the percentage of days underimmunised from birth to 19 months for 22 doses of eight vaccines recommended during this interval. Secondary outcomes include clinician experience communicating with VHPs, parent visit experience and clinician adherence to the PIVOT with MI communication strategy. ETHICS AND DISSEMINATION: This study is approved by the following institutional review boards: Colorado Multiple Institutional Review Board, Washington State Institutional Review Board and Swedish Health Services Institutional Review Board. Results will be disseminated through peer-reviewed manuscripts and conference presentations. TRIAL REGISTRATION NUMBER: NCT03885232.
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spelling pubmed-74186712020-08-18 ‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention Opel, Douglas J Robinson, Jeffrey D Spielvogle, Heather Spina, Christine Garrett, Kathleen Dempsey, Amanda F Perreira, Cathryn Dickinson, Miriam Zhou, Chuan Pahud, Barbara Taylor, James A O'Leary, Sean T BMJ Open Paediatrics INTRODUCTION: A key contributor to underimmunisation is parental refusal or delay of vaccines due to vaccine concerns. Many clinicians lack confidence in communicating with vaccine-hesitant parents (VHP) and perceive that their discussions will do little to change parents’ minds. Improving clinician communication with VHPs is critical to increasing childhood vaccine uptake. METHODS AND ANALYSIS: We describe the protocol for a cluster randomised controlled trial to test the impact of a novel, multifaceted clinician vaccine communication strategy on child immunisation status. The trial will be conducted in 24 primary care practices in two US states (Washington and Colorado). The strategy is called Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing (PIVOT with MI), and involves clinicians initiating the vaccine conversation with all parents of young children using the presumptive format, and among those parents who resist vaccines, pivoting to using MI. Our primary outcome is the immunisation status of children of VHPs at 19 months, 0 day of age expressed as the percentage of days underimmunised from birth to 19 months for 22 doses of eight vaccines recommended during this interval. Secondary outcomes include clinician experience communicating with VHPs, parent visit experience and clinician adherence to the PIVOT with MI communication strategy. ETHICS AND DISSEMINATION: This study is approved by the following institutional review boards: Colorado Multiple Institutional Review Board, Washington State Institutional Review Board and Swedish Health Services Institutional Review Board. Results will be disseminated through peer-reviewed manuscripts and conference presentations. TRIAL REGISTRATION NUMBER: NCT03885232. BMJ Publishing Group 2020-08-11 /pmc/articles/PMC7418671/ /pubmed/32784263 http://dx.doi.org/10.1136/bmjopen-2020-039299 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Paediatrics
Opel, Douglas J
Robinson, Jeffrey D
Spielvogle, Heather
Spina, Christine
Garrett, Kathleen
Dempsey, Amanda F
Perreira, Cathryn
Dickinson, Miriam
Zhou, Chuan
Pahud, Barbara
Taylor, James A
O'Leary, Sean T
‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention
title ‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention
title_full ‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention
title_fullStr ‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention
title_full_unstemmed ‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention
title_short ‘Presumptively Initiating Vaccines and Optimizing Talk with Motivational Interviewing’ (PIVOT with MI) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention
title_sort ‘presumptively initiating vaccines and optimizing talk with motivational interviewing’ (pivot with mi) trial: a protocol for a cluster randomised controlled trial of a clinician vaccine communication intervention
topic Paediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418671/
https://www.ncbi.nlm.nih.gov/pubmed/32784263
http://dx.doi.org/10.1136/bmjopen-2020-039299
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