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Study identifier: NCT06135636 Synced from ClinicalTrials.gov · July 28, 2026
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Assessing Interventions to Increase Tdap Acceptance for Non-birthing Partners in Pregnancy

Condition: Non-birthing Partner Vaccination in Pregnancy · Tdap - Tetanus, Diphtheria and Acellular Pertussis Vaccination · Vaccine Exposure During Pregnancy  ·  Sponsor: Women and Infants Hospital of Rhode Island

PhasePhase 4
Planned participants150
Who can joinAll sexes, 19 Years to 50 Years
Healthy volunteersYes

About this study

The goal of this randomized control trial is to assess if prenatal vaccine education and in-office vaccination administration for non-birthing partners of pregnant patients increases Tdap vaccination rates compared to usual care. The main question\[s\] it aims to answer are: * To assess whether compared to standard prenatal care, targeted prenatal education regarding Tdap vaccination recommendations with and without in office vaccination opportunities improves Tdap uptake among non-birthing partners of pregnant patients. * To assess whether non-birthing partners presenting for Tdap vaccination are willing to accept dual vaccination with Tdap and influenza. Participants will receive direct verbal and written education at the time of enrollment on cocooning and recommendation for partner Tdap vaccination prior to delivery with or without the option to receive Tdap at their convenience at the WIH obstetric care clinic. If there is a comparison group: Researchers will compare "Upfront Education" and "Upfront Education and Vaccination Administration" to "Usual care" to see if education and/or the offer for vaccination in the office increases Tdap vaccine acceptance for non-birthing partners.

This description comes directly from the study's public registry record.

Talk to the study team

Laurie Griffin, MD/PhD  ·  9785182135  ·  LGRIFFIN@WIHRI.ORG

Adam Lewkowitz, MD/MPHS  ·  401-274-1122  ·  Alewkowitz@kentri.org

Always discuss trial participation with your own doctor first.

Locations (1)

Women and Infants HospitalProvidence, Rhode Island, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06135636