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.
Study Type
OBSERVATIONAL
Enrollment
1,200
This study will not administer any treatment, only observe the treatment as prescribed in real-world clinical practice
Paratus Clinical Research
Brisbane, Queensland, Australia
The proportion of immunised infants among all enrolled infants
A descriptive analysis of immunisation status (yes/no) will be performed using summary statistics.
Time frame: March 2026-May 2026
Type of immunisation
A descriptive analysis of immunisation status (yes/no) will be performed using summary statistics.
Time frame: March 2026-May 2026
Location of immunization
A descriptive analysis of immunisation status (yes/no) will be performed using summary statistics.
Time frame: March 2026-May 2026
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