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Using provider–parent strategies to improve influenza vaccination in children and adolescents with special risk medical conditions: a randomised controlled trial protocol

Authors :
Jane Tuckerman
Kelly Harper
Thomas R Sullivan
Jennifer Fereday
Jennifer Couper
Nicholas Smith
Andrew Tai
Andrew Kelly
Richard Couper
Mark Friswell
Louise Flood
Margaret Danchin
Christopher C Blyth
Helen Marshall
Tuckerman, Jane
Harper, Kelly
Sullivan, Thomas R
Fereday, Jennifer
Couper, Jennifer
Smith, Nicholas
Tai, Andrew
Kelly, Andrew
Couper, Richard
Friswell, Mark
Flood, Louise
Danchin, Margaret
Blyth, Christopher C
Marshall, Helen
Source :
BMJ Open, Vol 12, Iss 2 (2022)
Publication Year :
2022
Publisher :
BMJ, 2022.

Abstract

IntroductionInfluenza immunisation is a highly cost-effective public health intervention. Despite a comprehensive National Immunisation Program, influenza vaccination in children and adolescents with special risk medical conditions (SRMCs) is suboptimal. Flutext-4U is an innovative, multi-component strategy targeting paediatric hospitals, general practice and parents of children and adolescents with SRMC. The Flutext-4U study aims to assess the impact of Flutext-4U to increase influenza immunisation in children and adolescents with SRMC.Methods and analysisThis is a randomised controlled trial involving parents of children and adolescents (aged >6 months to Parents (of children/adolescents with SRMC) are randomised (1:1 ratio) to standard care plus intervention (SMS reminder messages to parents; reminders (written correspondence) for their child’s GP from the hospital’s Paediatric Outpatients Department) or standard care (hospital vaccine availability, ease of access and reminders for WCH subspecialists) with randomisation stratified by age-group (14 to The primary outcome is influenza vaccination, as confirmed by the Australian Immunisation Register.The proportion vaccinated (primary outcome) will be compared between randomised groups using logistic regression, with adjustment made for age group at randomisation. The effect of treatment will be described using an OR with a 95% CI.Ethics and disseminationThe protocol and all study materials have been reviewed and approved by the Women’s and Children’s Health Network Human Research Ethics Committee (HREC/20/WCHN/5). Results will be disseminated via peer-reviewed publication and at scientific meetings, professional and public forums.Trial registration numberAustralian New Zealand Clinical Trials Registry (ACTRN12621000463875).

Details

ISSN :
20446055
Volume :
12
Database :
OpenAIRE
Journal :
BMJ Open
Accession number :
edsair.doi.dedup.....cea18f8542b31a5b1e75093d2794f06f
Full Text :
https://doi.org/10.1136/bmjopen-2021-053838