Vaccine Acceptance in Pregnant Minority Women

NACompletedINTERVENTIONAL
Enrollment

121

Participants

Timeline

Start Date

July 31, 2012

Primary Completion Date

July 31, 2014

Study Completion Date

July 31, 2014

Conditions
Pregnancy
Interventions
BEHAVIORAL

Maternal Vaccine Education

It is assumed that the women will also receive vaccine education materials from the OB/GYN practices as part of routine care. The intervention for all three arms will be conducted during routine prenatal office visits. Participants will complete a baseline questionnaire to assess attitudes regarding vaccination and will then be randomized to one of three enrollment arms and will be exposed to an intervention designed to take no longer than 20 minutes, so that patients can complete it during the time they are waiting to be seen. While participants are completing the handheld/electronic tablet device-based intervention, the study recruiter will observe them and document dose exposure to the messages being presented. The enrolled women will be contacted a month after the expected date of delivery and a follow up interview will be conducted to ascertain their vaccination status for receipt of influenza vaccine in pregnancy and Tdap during pregnancy or immediately post-partum.

Trial Locations (4)

30033

Dourron OB/Gyn Associates Clinic, Decatur

30274

New Millenium Obstetrics & Gynecology, Riverdale

30303

Grady Health System, Atlanta

30308

Emory University Hospital Midtown, Atlanta

All Listed Sponsors
collaborator

Kaiser Permanente

OTHER

lead

Emory University

OTHER

NCT01740310 - Vaccine Acceptance in Pregnant Minority Women | Biotech Hunter | Biotech Hunter