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NCT03497936

Marketability of a Technology-based Intervention to Increase HPV Vaccination

Completed NA Last updated 19 September 2022
What this trial tests

NA trial testing Women's Stories in Human Papilloma Virus in 360 participants. Completed in 29 March 2021.

Timeline
1 May 2018
Primary endpoint
29 March 2021
29 March 2021

Quick facts

Lead sponsorReal Prevention, LLC
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment360
Start date1 May 2018
Primary completion29 March 2021
Estimated completion29 March 2021
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Real Prevention, LLC

Who can join

Adults 18 to 26, female only, with Human Papilloma Virus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The overall goal of this SBIR Phase II project is to reduce cancer rates by marketing a brief, easily implemented technology-based intervention that increases human papillomavirus (HPV) vaccination among Planned Parenthood and other clients. The intervention's innovative technology allows for the investigators' narrative videos to be presented along will reminder texts. It will be evaluated for use in waiting rooms and promises to overcome vaccination barriers among high risk but underserved low SES and minority populations.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Human Papilloma Virus

Currently open trials in the same condition.

Other Real Prevention, LLC trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03497936.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing