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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04208269
Other study ID # IRB201200143
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2013
Est. completion date March 30, 2015

Study information

Verified date May 2020
Source University of Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our project will assess the feasibility and estimate preliminary efficacy of a multilevel intervention to improve HPV vaccine series initiation among adolescents in Medicaid and CHIP. The investigators will use two intervention components: postcards and an iPad survey system. To estimate efficacy the investigators will select potential participants from Florida Medicaid and CHIP. The investigators will assess their claims for the HPV vaccine before and after the intervention.


Recruitment information / eligibility

Status Completed
Enrollment 5663
Est. completion date March 30, 2015
Est. primary completion date April 1, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 11 Years to 18 Years
Eligibility Inclusion Criteria:

- Enrolled in Florida Medicaid

- Not initiated the HPV vaccine series at the start of the study period.

Exclusion Criteria:

- Anyone who has a severe (life threatening) allergy to any component of HPV vaccine, esp yeast

- Pregnant

- Not enrolled in Florida Medicaid

Study Design


Related Conditions & MeSH terms


Intervention

Other:
postcard campaign
Post card sent to parent only
Health Information Technology system
Accessed by adolescent and provider only

Locations

Country Name City State
United States University of Florida Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of participants receiving HPV vaccine The percent age eligible participants who initiate HPV vaccination. Up to 5 months
Primary Number of preventive care visits The percent age eligible participants received a preventive care visit Up to 3 months
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