Vaccination Clinical Trial
Official title:
The Acceptability of the HPV Vaccine Postpartum and With Pediatric Well-child Visits: A Pilot Study
The purpose of this study is to determine if women would find it acceptable to receive the HPV vaccine postpartum at the pediatrician's office at the time of their child's two-month well- child visit when offered during the third trimester of pregnancy.
There are a large number of young adult women who have not received any doses of HPV vaccine
or are incompletely vaccinated. Recommendation for HPV vaccine could occur during pregnancy
with the administration of the vaccine postpartum. Finding a way to make it easy for women
to present for vaccination is imperative as this is currently a 3-vaccine series. The
investigators are interested in understanding if women would find it acceptable if the
investigators discussed and encouraged the vaccine while pregnant with receipt of the
vaccine through their child's pediatrician at well-child visits in the postpartum period.
The investigators will survey women in the third trimester of pregnancy to determine if they
would find this acceptable and follow-up with them after their child's two month pediatric
visit to reevaluate their opinion. No doses of the vaccine will be given.
The investigators are also interested in understanding other factors that could affect
whether or not women would be interested in receiving the HPV vaccine postpartum. This
includes rates of attendance at postpartum visits as well as behavioral, knowledge and
demographic characteristics that may be associated with acceptability of receiving the
vaccine.
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