Adults 15 to 29, male only, with HIV Infections or Sexually Transmitted Diseases. 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.
Percent of Participants Reporting Changes in Their HIV Testing Behavior Using Self-report QuestionnairesPrimary· 12 month
The investigators will estimate the proportion of participants who test at least twice for HIV over a 12-month period by intervention group.
Group
Value
95% CI
Information-Only Arm
185
HMP 2.0 Arm
171
Peer-referred HMP Network Arm
2
Percent of Participants Reporting Viral Suppression Using Self-Report QuestionnairesPrimary· 12 month
The investigators will estimate the proportion of participants living with HIV who achieve viral suppression over a 12-month period by intervention group.
Group
Value
95% CI
Information-Only Arm
45
HMP 2.0 Arm
60
Peer-referred HMP Network Arm
60
Information-Only Arm
29
HMP 2.0 Arm
15
Peer-referred HMP Network Arm
21
Number of Days in the Prior Week That Participants Self-report Missing at Least One Dose of Their Adherence to Antiretroviral Therapy (ART) Using a Self-Reported QuestionnaireSecondary· 12 month
The investigators will test the proportion of the HIV-positive sample that adheres to their HIV care regimen during the 12-month follow-up.
Group
Value
95% CI
Information-Only Arm
0.92
± 1.65
HMP 2.0 Arm
0.96
± 1.75
Peer-referred HMP Network Arm
1.21
± 2.06
Percent of Participants Reporting PrEP Uptake Using Self-Report QuestionnairesSecondary· 12 month
The investigators will test the proportion of the HIV-negative sample that reports using PrEP by the 12-month follow-up.
Group
Value
95% CI
Information-Only Arm
77
HMP 2.0 Arm
74
Peer-referred HMP Network Arm
0
Information-Only Arm
50
HMP 2.0 Arm
42
Peer-referred HMP Network Arm
1
Information-Only Arm
78
HMP 2.0 Arm
73
Peer-referred HMP Network Arm
1
Sponsor's own description
The overall goal of this 3-arm randomized trial is to test whether a network-driven online intervention tailored for intersectional stigma amelioration can elicit online social support, promote intervention engagement, and mitigate the impact of multiple stigmas on HIV-related outcomes among young Black and/or Latino men who have sex with men and transgender women.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
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· NA
· recruiting
NCT07202546 — A Phase 2b Study Evaluating Oral VH4524184 Regimens in Treatment Naïve Persons With HIV-1 (INNOVATE Study)
· Phase 2
· recruiting
NCT06694753 — Safety and Immunogenicity Study of Three mRNAs Encoding HIV Immunogens in Adult Participants Without HIV and in Overall
· Phase 1
· recruiting
NCT07235852 — Pilot Testing Into the Feasibility of the Developed Cognitive Behavioral Therapy Intervention
· NA
· recruiting
NCT06665646 — Clinical Trial to Evaluate the Safety and Immunogenicity of Hiltonol, Poly-ICLC-adjuvanted CD40.HIVRI.Env (VRIPRO) in Ad
· Phase 1
· recruiting
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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 University of Pennsylvania
Last refreshed: 27 September 2024
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/NCT03678181.