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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01087164 |
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Date of registration:
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02/02/2009 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Brief Interventions to Increase HPV Vaccine Acceptance in School-based Health Centers
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Scientific title:
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Brief Interventions to Increase HPV Vaccine Acceptance in School-based Health Centers in Adolescents |
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Date of first enrolment:
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September 2010 |
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Target sample size:
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600 |
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Recruitment status: |
Active, not recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01087164 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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United States
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Contacts
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Name:
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Vaughn I Rickert, PsyD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Indiana University School of Medicine |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- The parents of adolescent males and females (aged 11-14 years) who have provided
written consent for their adolescent to receive health care services through the Teen
Health Center, Inc, a nonprofit organization that works in collaboration with the
Department of Pediatrics at the University of Texas Medical Branch, Galveston, Texas
and whose adolescents have not received their first dose of HPV vaccine, will be
eligible to participate.
Exclusion Criteria:
- Having received one or more doses of the HPV vaccine Gardasil
Age minimum:
11 Years
Age maximum:
15 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Human Papillomavirus Infection
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Intervention(s)
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Behavioral: Message sidedness
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Behavioral: Compliance
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Primary Outcome(s)
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Gardasil immunization
[Time Frame: One year]
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Secondary Outcome(s)
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Message type
[Time Frame: Two years]
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Gender
[Time Frame: One year]
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Completion of three dose series of Gardasil
[Time Frame: Three years]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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