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Evaluating Post-test HIV Counseling Videos for Teens

NCT ID: NCT00851539

Last Updated: 2014-12-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-06-30

Study Completion Date

2011-04-30

Brief Summary

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The design of this randomized controlled trial (RCT) is to test the effectiveness of a post-test behavioral video in educating adolescents about HIV transmission and affecting their intentions to engage in risk-reduction behavior.

Detailed Description

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Adolescents are at risk for HIV because of their engagement in high risk sexual activity. This study seeks to determine effective ways to educate teens about HIV and how to protect themselves by use of multimedia. All eligible participants who agree to enroll in this trial will be randomized into two arms: the behavioral intervention video (intervention group) or meeting with an in-person counselor (control group) as they wait for their rapid HIV results. The goals of the RCT involve establishing the feasibility of using touch-screen technology for teenagers in the ED; establishing the receptivity of teens to HIV rapid testing in the ED; providing data on rates, and obtaining preliminary data on the effectiveness of the video in changing condom efficacy, condom outcome expectancies and condom use intention. Consenting to rapid HIV testing is a secondary outcome.

Conditions

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HIV HIV Infections

Keywords

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HIV Teenagers Adolescent HIV Testing HIV Seronegativity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Caregivers

Study Groups

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Control

Participants received counseling from a live counselor.

Group Type NO_INTERVENTION

No interventions assigned to this group

Video

Behavioral Intervention Video

Group Type EXPERIMENTAL

Video

Intervention Type BEHAVIORAL

Behavioral Intervention Video

Interventions

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Video

Behavioral Intervention Video

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Youth who have had vaginal, anal or oral sex
2. 15-21 years of age
3. English speaking

Exclusion Criteria

1. Clinically unstable secondary to pain or unstable vitals signs
2. Unable to understand the consent process for the study
3. Known HIV status or recent HIV test
4. Language other than English
Minimum Eligible Age

15 Years

Maximum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NIH

Sponsor Role collaborator

North Bronx Healthcare Network

OTHER

Sponsor Role lead

Responsible Party

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Yvette Calderon,MD, MS

Professor of Clinical Emergency Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Yvette Calderon, MD MS

Role: PRINCIPAL_INVESTIGATOR

Jacobi Medical Center/ Albert Einstein Medical College

Locations

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Jacobi Medical Center

The Bronx, New York, United States

Site Status

Countries

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United States

References

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Calderon Y, Cowan E, Leu CS, Brusalis C, Rhee JY, Nickerson J, Leider J, Bauman LJ. A human immunodeficiency virus posttest video to increase condom use among adolescent emergency department patients. J Adolesc Health. 2013 Jul;53(1):79-84. doi: 10.1016/j.jadohealth.2013.01.028. Epub 2013 Apr 9.

Reference Type DERIVED
PMID: 23582525 (View on PubMed)

Other Identifiers

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5K23HD054315

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2006-443

Identifier Type: -

Identifier Source: org_study_id