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An HPV Vaccine Provider Intervention in Safety Net Clinics

NCT02808832 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 806

Last updated 2016-09-14

No results posted yet for this study

Summary

The purpose of this study is to develop, deliver and evaluate a provider intervention for mothers and their children to encourage receipt of the human papillomavirus (HPV) vaccine in the children and appropriate cervical cancer screening in the mothers.

Conditions

  • Human Papillomavirus
  • Uterine Cervical Neoplasms

Interventions

BEHAVIORAL

Educational materials

5-minute video and information sheet with a list of suggested questions to ask the provider

Sponsors & Collaborators

  • Vanderbilt University

    collaborator OTHER

  • Matthew Walker Comprehensive Health Center

    collaborator UNKNOWN

  • Memphis Health Center

    collaborator UNKNOWN

  • Southside/Dodson Avenue Community Health Centers

    collaborator UNKNOWN

  • Meharry Medical College

    lead OTHER

Principal Investigators

  • Maureen Sanderson, PhD · Meharry Medical College

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
9 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2016-03-31
Completion
2016-08-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02808832 on ClinicalTrials.gov