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Clinical Trials/NCT02049710
NCT02049710
Completed
Not Applicable

Randomized Controlled Trial Evaluating the Effectiveness of Interactive Video Interventions to Reduce Teen Pregnancy and Teen Automobile Injuries

Carnegie Mellon University3 sites in 1 country1,317 target enrollmentJune 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pregnancy
Sponsor
Carnegie Mellon University
Enrollment
1317
Locations
3
Primary Endpoint
Perceived Self-efficacy for Condom Use
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to measure the effects of an interactive video on adolescent risky behaviors and outcomes, with one video intended to reduce teen pregnancies and the other intended to reduce automobile accidents.

Detailed Description

Motor vehicle crashes cause one-third of teenage deaths and many serious injuries. Teen drivers ages 16 to 19 are four times more likely than older drivers to crash. Death and injuries could be reduced with a change in behaviors that include improved visual and attention skills while driving, more seat belt use, appropriate speed control, and not combining drinking or texting with driving. Sexually transmitted infections (STIs) and unplanned pregnancies are particularly common among adolescents. The U.S. adolescent birthrate is by far the highest among industrialized nations. These problems can be decreased by less sexual activity and better protection. This study uses a randomized controlled trial to measure how well interactive video interventions can reduce these common risks to adolescents. Adolescent females will be invited to participate if they are currently seeking care at a participating clinic. They will answer survey questions about their driving and sexual behaviors, and then a computer will determine whether they will be given a video about driving or a video about sexual behavior. Participants will have unlimited access to their video, which they can watch at their clinic or from any Internet-enabled computer, and will be followed for 6 months.

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
August 2016
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient at participating healthcare facility
  • Unmarried at time of enrollment
  • Not pregnant at time of enrollment
  • Available for contact over ensuing 6 months

Exclusion Criteria

  • Apparent or stated inability to comprehend consent or assent form (e.g., language barrier or cognitive ability)
  • No ability to provide at least 2 methods of contact
  • Married or pregnant at time of enrollment

Outcomes

Primary Outcomes

Perceived Self-efficacy for Condom Use

Time Frame: 6 months

To assess the effects of the Seventeen Days interactive video on young women's perceived self-efficacy for using condoms 6 months after being offered the intervention, relative to a control.

Study Sites (3)

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