An Adaptive Prenatal Intervention to Increase Childhood Vaccinations

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Conditions studied: Vaccination Refusal

In brief

This study will test whether proactively connecting expectant parents with factual vaccination information during pregnancy can build confidence in vaccinations and lead to timely vaccinations during pregnancy and once their child is born.

Key facts

Study ID

NCT05795855

Run by

Emory University

People needed

770

Starts

2024-04-27

Expected to finish

2026-08-31

Last updated by the study team

2026-01-07

Who can join

Age: any. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Nulliparous individuals (no prior live birth)
• Singleton pregnancy (excludes twins, triplets, etc.)
• No known fetal congenital malformations or genetic abnormalities
• Not at known risk for preterm birth
• In late second trimester during study recruitment period
• Receive prenatal care at one of the study practices
• Inclusion Criteria for Nested Sub-Study:
• Eligible to receive adaptive components of ADEPT (vaccine-hesitant after provider recommendation)
• At least 18 years of age
• Provide informed consent
• Agree to participate in surveys and in-depth interview
• Agree for child's vaccination outcomes to be extracted from the North Carolina Immunization Registry (NCIR)
• Plan to stay in North Carolina for at least 3 months after delivery

You may not qualify if…

• none

Where it is running

• Duke Health System — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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