Vaccine in pregnancy Other
Conditions
Interventions
This is a qualitative study involving semi-structured interviews with pregnant women (focus groups will also be offered to pregnant women if they prefer) and clinicians involved in the care of pregnan
Sponsors
University of Birmingham
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Pregnant women: Pregnant women at any stage of pregnancy, with any vaccination history. Pregnant women will be over the age of 18 years, with the capacity to consent. Translation services will be used for interviews where English is not the first language, but participants are required to be able to read the participant information sheet in English. Clinicians: Clinicians working with or providing care to pregnant women, including (but not limited to) GPs, midwives, nurses and community pharmacists. Clinicians will be over the age of 18 years.
Exclusion criteria
Exclusion criteria: Any participant who does not have the capacity to consent, or is unable to read the study information in English will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measured by interviews at approximately 6, 9 and 12 months: 1. Pregnant women’s information preferences and needs about vaccination using qualitative interviews 2. Clinicians’ views on pregnant women’s information needs using qualitative interviews 3. Key features and guiding principles for an intervention to increase uptake of vaccination amongst pregnant women 4. User feedback on the intervention at various stages of development using qualitative interviews Thematic analysis will be used for analysis. | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
England, United Kingdom
Contacts
Public ContactJo Parsons
Outcome results
None listed