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Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial
BACKGROUND: Pregnant women are the highest priority group for annual influenza vaccination. Studies have shown unacceptably low uptake of both seasonal and pandemic A/H1N1 influenza vaccination among pregnant women. This paper will describe the study protocol and methodology of a randomised controll...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898030/ https://www.ncbi.nlm.nih.gov/pubmed/24423245 http://dx.doi.org/10.1186/1471-2393-14-19 |
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author | Wong, Valerie WY Fong, Daniel YT Tarrant, Marie |
author_facet | Wong, Valerie WY Fong, Daniel YT Tarrant, Marie |
author_sort | Wong, Valerie WY |
collection | PubMed |
description | BACKGROUND: Pregnant women are the highest priority group for annual influenza vaccination. Studies have shown unacceptably low uptake of both seasonal and pandemic A/H1N1 influenza vaccination among pregnant women. This paper will describe the study protocol and methodology of a randomised controlled trial designed to assess the effectiveness of a brief educational intervention in improving the uptake of seasonal influenza vaccine among pregnant women in Hong Kong. METHODS: A randomised controlled trial will be conducted with pregnant women in at least the second trimester of pregnancy from four publicly funded hospital antenatal clinics in Hong Kong. Participants will be randomly assigned to either one of the two treatment groups: standard care (control) or standard care plus brief education (intervention). Pregnant women in the standard care group will receive the usual antenatal care with an educational pamphlet developed by the Hong Kong Centre for Health Protection and those in the intervention group will be provided with usual care plus a brief ten-minute education intervention. Content of the education session will cover four core components recommended in the research literature. The primary study outcome will be the proportion of participants who have received influenza vaccine during their pregnancy. A total of 184 pregnant women (92 per group) will be required to give an 80% power to detect a treatment effect of 15%. DISCUSSION: Most intervention studies aimed at improving influenza vaccination rates in pregnant women have targeted obstetric-care providers and the results of the two patient-oriented RCT interventions are conflicting. The high priority for vaccination given to pregnant women and the low influenza vaccination rate among pregnant women worldwide strongly indicates a need for interventions to improve uptake. TRIAL REGISTRATION: This trial is registered with the Clinical Trials Registry at www.clinicaltrials.gov(NCT01772901). |
format | Online Article Text |
id | pubmed-3898030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38980302014-01-23 Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial Wong, Valerie WY Fong, Daniel YT Tarrant, Marie BMC Pregnancy Childbirth Study Protocol BACKGROUND: Pregnant women are the highest priority group for annual influenza vaccination. Studies have shown unacceptably low uptake of both seasonal and pandemic A/H1N1 influenza vaccination among pregnant women. This paper will describe the study protocol and methodology of a randomised controlled trial designed to assess the effectiveness of a brief educational intervention in improving the uptake of seasonal influenza vaccine among pregnant women in Hong Kong. METHODS: A randomised controlled trial will be conducted with pregnant women in at least the second trimester of pregnancy from four publicly funded hospital antenatal clinics in Hong Kong. Participants will be randomly assigned to either one of the two treatment groups: standard care (control) or standard care plus brief education (intervention). Pregnant women in the standard care group will receive the usual antenatal care with an educational pamphlet developed by the Hong Kong Centre for Health Protection and those in the intervention group will be provided with usual care plus a brief ten-minute education intervention. Content of the education session will cover four core components recommended in the research literature. The primary study outcome will be the proportion of participants who have received influenza vaccine during their pregnancy. A total of 184 pregnant women (92 per group) will be required to give an 80% power to detect a treatment effect of 15%. DISCUSSION: Most intervention studies aimed at improving influenza vaccination rates in pregnant women have targeted obstetric-care providers and the results of the two patient-oriented RCT interventions are conflicting. The high priority for vaccination given to pregnant women and the low influenza vaccination rate among pregnant women worldwide strongly indicates a need for interventions to improve uptake. TRIAL REGISTRATION: This trial is registered with the Clinical Trials Registry at www.clinicaltrials.gov(NCT01772901). BioMed Central 2014-01-14 /pmc/articles/PMC3898030/ /pubmed/24423245 http://dx.doi.org/10.1186/1471-2393-14-19 Text en Copyright © 2014 Wong et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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. |
spellingShingle | Study Protocol Wong, Valerie WY Fong, Daniel YT Tarrant, Marie Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial |
title | Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial |
title_full | Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial |
title_fullStr | Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial |
title_full_unstemmed | Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial |
title_short | Brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial |
title_sort | brief education to increase uptake of influenza vaccine among pregnant women: a study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898030/ https://www.ncbi.nlm.nih.gov/pubmed/24423245 http://dx.doi.org/10.1186/1471-2393-14-19 |
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