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eKISS Electronic KIOSK Intervention for Safer-Sex: A Pilot Randomized Controlled Trial of an Interactive Computer-based Intervention for Sexual Health in Adolescents and Young Adults (NCT03027531)

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
This study is a randomized controlled trial to test acceptability, feasibility and preliminary efficacy of an interactive computer-based intervention with individualized feedback to promote sexual health in adolescents and young adults with assessment of behavioral and biomarker outcomes.
  • : 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.
    Ages eligible for Study
    14 Years to 24 Years
    Genders eligible for Study
    All
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Inclusion Criteria:
    • English speaking and reading
    • 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:
    • Currently pregnant or actively seeking pregnancy in self or partner
    This study is a randomized controlled trial to test acceptability, feasibility and preliminary efficacy of an interactive computer-based intervention (ICBI) with individualized feedback to promote sexual health in adolescents and young adults. The intervention uses physician avatars and uses elements of motivational interviewing to elicit sexual risk behaviors and motivation to change risky behavior. Feedback includes instructive video modules. Participants were asked to identify one behavior to change and were reassessed at 3-month follow-up for interim sexual behavior including condom and birth control use. Participants were tested for chlamydia, gonorrhea, and pregnancy(females) at baseline and 3-month follow-up.
    Status:
    unknown
    Type:
    Interventional
    Phase:
    -
    Start:
    31 January, 2012
    Updated:
    19 January, 2017
    Participants:
    272
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