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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00680147
Other study ID # IISP ID# 33546
Secondary ID
Status Completed
Phase Phase 2
First received May 15, 2008
Last updated May 19, 2015
Start date July 2008
Est. completion date February 2012

Study information

Verified date May 2015
Source Syracuse University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This will enroll 300 mothers of teenage girls and boys to identify barriers to HPV vaccination among low-income, African-American teens.


Description:

The HPV vaccine offers hope that the incidence of cervical cancer can be greatly reduced in the U.S. and globally. However, because the vaccine is recommended for children and early adolescents, vaccine awareness and acceptance among parents is critical to insuring vaccine uptake and public health benefit. Although culturally specific concerns may reduce HPV vaccination among African-American youth, research has not addressed this possibility. Accordingly, the proposed study will enroll 300 mothers in a study to identify barriers to HPV vaccination among low-income, African-American teens. Surveys assessing culturally-specific barriers to HPV vaccination acceptance will be administered to both parents and their vaccine-eligible children. Upon completion of the survey, parents with vaccine-eligible daughters will be invited to receive a free HPV vaccination for their child through a local, teen-friendly health clinic. Outcome analyses will focus on identification of predictors of completed vaccinations among girls and barriers to vaccine acceptance among mothers of teenage sons. Our study will provide critically important behavioral outcome data linking barriers to vaccination to subsequent vaccination decisions in a real-world, health care setting.


Recruitment information / eligibility

Status Completed
Enrollment 614
Est. completion date February 2012
Est. primary completion date February 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 11 Years and older
Eligibility Inclusion Criteria:

- Females parent or guardian with an African-American daughter or son between the ages of 11 and 17

- African-American adolescents between the ages of 11-17

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
brief informational intervention to promote HPV vaccine acceptance
Teen and parent participants will receive a brief informational intervention that provides basic facts about the HPV vaccine, including the health benefits and three-dose requirements, along with information regarding where to go to receive the vaccination. A coupon for a free HPV vaccination will provided to the parent for use by their teenage daughter.

Locations

Country Name City State
United States Center for Health and Behavior, Syracuse University Syracuse New York

Sponsors (1)

Lead Sponsor Collaborator
Syracuse University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary completed vaccination with Gardasil 6 months No
Secondary assessed cross-sectionally, at time of initial enrollment assessed at time of baseline assessment No
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