RSV Immunisation Status in Queensland (Australia)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSanofi

About this trial

The primary objective of this study is to determine the nirsevimab immunisation rate in eligible infants (according to Queensland Paediatric Respiratory Syncytial Virus Prevention Program recommendation) in Queensland, Australia.

The study will focus on:

1\. Assessing the immunisation rates among eligible infants (born from 1 February 2024 to 15 April 2025) in their first Respiratory Syncytial Virus (RSV)-season in Queensland.

Secondary objectives of this study are as follows:

1. To analyse reasons of parents to decide for or against immunisation of their infant with nirsevimab.

1. This objective aims to assess potential influencing factors and evaluate the changes in acceptance across the three cohorts prior and post recommendation. 2. In this regard, demographic factors (e.g. education, income) will be included in the analysis where applicable to gain insights on their potential impact. 2. To assess immunisation rates for further subgroups, e.g. by: a) risk group (defined chronic condition or pre-term birth status), b) regional areas of Queensland. 3. To compare the vaccination coverage rate estimates with data captured via the Australian Immunisation Register.

Eligibility criteria

Qualifiers

Be a parent of an infant born between 1 February 2024 and 15 April 2025

Be at least 18 years of age

Reside in Queensland, Australia

Read and agree to the Participant Information and Consent Form (PICF) before proceeding to the survey

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Nirsevimab Respiratory Syncytial Virus monoclonal antibody

Treatment groups

1,200 Participants
are divided into 1 treatment group

Sponsors and collaborators