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NCT01600560 · ClinicalTrials.gov registry record

Facilitating Completion of HPV Vaccination

A clinical trial, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
223
Enrollment target

NCT01600560 is a clinical trial that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 223 participants.

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The verdict

NCT01600560 has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
223 participants
Enrollment target

Study Summary

With the surge in use of electronic media among adolescents, a strategy that has been utilized to increase HPV4 uptake in girls has been reminder text messaging to their parents. To date, no published study has looked at the effectiveness of texting adolescents themselves (especially boys) rather than their parents OR compared texting to social network sites to increase HPV knowledge and uptake of HPV vaccination in boys. Interactive technology-based interventions targeted at youth are feasible in North Carolina for the following reasons: (1) through the NC Minors' Consent Law adolescents can consent to the prevention, diagnosis, and treatment of sexually transmitted diseases (N.C. Gen. Stat. § 90-21.5(a); and (2) many school based health centers can provide immunizations. Since HPV infection is a sexually transmitted infection, NC teens do not have to get consent for HPV prevention (i.e., vaccination). To optimize HPV vaccination in young people, especially males, communication strategies are needed to motivate adolescents to get themselves vaccinated. Texting has been demonstrated to be a feasible, popular, and effective method of sexual health promotion to young people with a relatively low withdrawal rate, positive feedback, and an observed improvement in sexual health knowledge and STI testing (12). Social media communication strategies are a new and potentially effective channel for communicating public health messages about HPV vaccine that are also likely to increase HPV initiation and completion among adolescent girls in addition to boys. According to the NC Immunization Registry, as of March 8, 2011, only 2% of boys ages 9-13 had received at least one dose of HPV vaccine. In the investigators continuity clinic less than 50 percent of adolescents are fully immunized. This project will identify social behavioral, emotional, and cognitive correlates and predictors that help explain why teens pursue, complete, and do not complete HPV vaccination, and develop

Trial Details

FieldValue
Enrollment Target 223 participants
Start Date 2012-05
Est. Completion 2016-07-05

What the Registry Record Tells You About NCT01600560

The ClinicalTrials.gov registry entry for NCT01600560 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 223 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 0 interventions.

NCT01600560 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01600560 about?

NCT01600560 is a clinical study titled "Facilitating Completion of HPV Vaccination". With the surge in use of electronic media among adolescents, a strategy that has been utilized to increase HPV4 uptake in girls has been reminder text messaging to their parents. To date, no published study has looked at the effectiveness of texting adolescents themselves (especially boys) rather th...

What is the current status of trial NCT01600560?

This trial is currently completed. The enrollment target is 223 participants. The study started on 2012-05. Estimated completion is 2016-07-05.

Who is sponsoring clinical trial NCT01600560?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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