HPV Vaccine Confident Families

NCT06002282•Rutgers, The State University of New Jersey

Summary

The objectives of the study are to pilot test a tailored intervention among Black families with adolescents. The hypotheses are that the study protocol will be feasible and messages tailored to parents' needs will increase vaccine confidence and intention to vaccinate.

Eligibility

Age

18 - 80 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•parent or legal guardian of at least one child aged 9-13 years who has received 0 or 1 dose of HPV vaccine;
•identify as Black or African American adult;
•have access to personal mobile phone and agree to send/receive MMS messages;
•able to speak and understand English; and
•able to provide informed consent to participate

Exclusion Criteria

•parent or legal guardian of child outside of participation age range or who has completed multiple doses of HPV vaccine;
•does not identify as Black or African American adult;
•does not have personal mobile phone;
•unable to speak and understand English;
•not willing to consent to participate

Locations (1)

Rutgers

New Brunswick, New Jersey, United States

Key Dates

Start Date

October 1, 2025

Primary Completion Date

June 1, 2026

Completion Date

July 1, 2026

Last Updated

August 11, 2025

Enrollment

ESTIMATED participants

Conditions

Human Papillomavirus Vaccines

Interventions

Tailored messages

BEHAVIORAL

Standard messages

BEHAVIORAL

Increasing Optimal Use of HPV Vaccination in Primary Care

NCT04180462

Human Papillomavirus Vaccines

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: August 11, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

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