Adults 16 to 30, any sex, with Exposure to Sexually Transmissible Disorder (Event). Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Feasibility as Assessed by the Number of Participants Who Are Enrolled With a PartnerPrimary· 24 months
Recruitment (as a measure of feasibility) will be assessed by calculating the number of eligible patients who return with a partner to the study appointment and consent to participate in the study.
Group
Value
95% CI
Control
17
Intervention
17
Acceptability as Assessed by Number of Participants Available for Week 6-8 InterviewSecondary· 6-8 weeks
Retention for the 6-8 week interview will also be calculated as a measure of acceptability.
Group
Value
95% CI
Control
27
Intervention
25
Sponsor's own description
This pilot project will evaluate the feasibility, acceptability, and preliminary effectiveness of a couples-based behavioral intervention \[COUPLES\] that augments individual evidence-based interventions with joint health education counseling for STI-affected AYA dyads within a primary care setting.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Johns Hopkins University
Last refreshed: 9 December 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03275168.