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Integrated Online-to-offline (O2O) Model of Care for HIV Prevention and Treatment Among Men Who Have Sex With Men

Study acronym: CINTAI
StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Study completion pushed from Aug 18, 2026 to Dec 18, 2026
    • Eligibility criteria expanded, about 6 words
    • Study description revised
  2. Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date changed from estimate of Dec 6, 2025 to Dec 10, 2025
    • Study completion date: May 18, 2026 to Aug 18, 2026
    • Site details revised
    v4
  3. Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Jan 6, 2025 to Dec 6, 2025
    • Study completion date: Feb 18, 2025 to May 18, 2026
    • Start date changed from estimate of May 19, 2024 to May 2, 2024
    • Site details revised
  4. Study description shortened, about 1 wordv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The proposed research focuses on developing and testing a web-based platform, called Jom-TestPlus, that will incorporate HIV self-testing (HIVST) with real-time e-counseling (eHIVST) with online-to-offline (O2O) linkage to HIV prevention and treatment services while simultaneously co-addressing chemsex-related needs for men who have sex with men (MSM) in Malaysia. This model represents a potentially impactful strategy for reaching marginalized populations, like MSM, and allows immediate engagement in the post-test linkage process to prevention or treatment services.
Trial Details
NCT Number NCT06373952
Lead Sponsor University of Connecticut
Collaborators: University of Malaya
Conditions
(from sponsor)		 HIV Prevention Program
Related terms Homosexuality
Enrollment 78 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov