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eKISS: Electronic KIOSK Intervention for Safer-Sex

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03027531
Acronym
eKISS
Enrollment
272
Registered
2017-01-23
Start date
2012-02-01
Completion date
2013-06-30
Last updated
2017-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contraception, Reproductive Behavior, Sexually Transmitted Diseases

Keywords

reproductive health, condoms, sexually transmitted diseases, contraception

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALeKISS: 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.

Sponsors

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
14 Years to 24 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Unprotected sex (no condoms) from self-report via computerized surveyduring last 2 months (asked at 3 month follow-up visit)number of unprotected sex events when participant did not use condom during sex

Secondary

MeasureTime frameDescription
Unprotected sex (no birth control) from self-report via computerized surveyduring last 2 months (asked at the 3-month follow-up visit)number of unprotected sex events when participant did not use birth control during sex
Number of sex partners from self-report via computerized surveyduring last 2 months (asked at the 3-month follow-up visit)number of partners with which the participant had sex
Biomarkers: urine sample tested with nucleic acid amplification test for STDs and urine sample pregnancy testover last 3 months (asked at the 3-month follow-up visit)Incident chlamydia, gonorrhea, and pregnancy since baseline visit

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026