RSV and vaccination in pregnancy

  • Research type

    Research Study

  • Full title

    Respiratory Syncytial Virus (RSV) and vaccination in pregnancy

  • IRAS ID

    220968

  • Contact name

    Christine Jones

  • Contact email

    c.e.jones@soton.ac.uk

  • Sponsor organisation

    University Hospital Southampton NHS Foundation Trust

  • Duration of Study in the UK

    0 years, 9 months, 1 days

  • Research summary

    Respiratory Syncytial Virus (RSV) is a very common virus that causes infection of the airways and lungs. It is the leading cause of chest infections (pneumonia and bronchiolitis) in young children, and is a major cause of admission to hospital and childhood death worldwide. Lots of research trials are being done into ways of preventing and treating RSV, however there is still no RSV vaccine approved for routine use. One possible way to protect the mother and young infant from RSV infection is a vaccine given to women during pregnancy, which would pass protection to their unborn child. This may help to prevent RSV in the child’s first few months of life when they are most vulnerable to infection. There are two vaccines that are currently being tested in pregnant women around the world, including the UK.

    With RSV vaccine candidates in the pipeline, this study aims to pre-emptively gauge the knowledge of RSV and potential acceptability of such vaccines amongst pregnant women and healthcare staff working in midwifery and obstetrics, as well as their attitudes (facilitators and barriers) to being involved in hypothetical future research trials.

    We propose to undertake a questionnaire-based study of randomly selected pregnant women and healthcare staff (over 16 years of age) at four English teaching hospitals. Pregnant women attending for ward reviews or antenatal clinics will approached and asked to complete an anonymous paper questionnaire lasting around 10 minutes. Healthcare staff will be approached in person, or via email, and asked to complete a slightly different questionnaire lasting around 5-10 minutes. No follow up will take place.

    We then, using statistical software, hope to identify factors that might affect their understanding of RSV and attitudes to being involved in hypothetical future trials and receiving the RSV vaccination

  • REC name

    London - West London & GTAC Research Ethics Committee

  • REC reference

    17/LO/0537

  • Date of REC Opinion

    6 Apr 2017

  • REC opinion

    Further Information Favourable Opinion