Study Results
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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COMPLETED
NA
272 participants
INTERVENTIONAL
2012-02-01
2013-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Control
Control group entered sexual history via computer assisted self-interview and provided specimens for chlamydia, gonorrhea and pregnancy(females) testing. The do not receive the feedback intervention of eKISS: electronic KIOSK for safer-sex
eKISS: electronic KIOSK for Safer-Sex
An interactive computer-based intervention for safer-sex which provides individualized feedback about protective and risky sexual behaviors; offers instructive video modules for safe-sex; elicits change behavior and identification of behavior change goal using elements of motivational interviewing.
Intervention
Intervention group entered sexual history via computer assisted self-interview and received the interactive computer-based intervention with individualized feedback eKISS: electronic KIOSK for safer-sex. They provided specimens for chlamydia, gonorrhea and pregnancy(females) testing.
eKISS: electronic KIOSK for Safer-Sex
An interactive computer-based intervention for safer-sex which provides individualized feedback about protective and risky sexual behaviors; offers instructive video modules for safe-sex; elicits change behavior and identification of behavior change goal using elements of motivational interviewing.
Interventions
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eKISS: electronic KIOSK for Safer-Sex
An interactive computer-based intervention for safer-sex which provides individualized feedback about protective and risky sexual behaviors; offers instructive video modules for safe-sex; elicits change behavior and identification of behavior change goal using elements of motivational interviewing.
Eligibility Criteria
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Inclusion Criteria
* Report at least one episode of unprotected vaginal sex (no condom OR no birth control) in the last 2 months
* Not currently pregnant or actively seeking pregnancy in self or partner
Exclusion Criteria
14 Years
24 Years
ALL
Yes
Sponsors
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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
NIH
University of Washington
OTHER
Responsible Party
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Taraneh Shafii
Associate Professor, Department of Pediatrics, Division of Adolescent Medicine
Principal Investigators
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Taraneh Shafii, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
University of Washington
King K Holmes, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Washington; Center for AIDS and STD
Other Identifiers
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32030-B
Identifier Type: -
Identifier Source: org_study_id
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