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Online Intervention for HIV

N/A
Waitlist Available
Led By Kate Muessig, PhD
Research Sponsored by University of Pennsylvania
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-month, 6-month, 9-month, and 12-month follow-up assessments
Awards & highlights

Study Summary

This trial is testing whether an online intervention can help reduce the negative impact of multiple stigmas on HIV-related outcomes for young Black and Latino men who have sex with men and transgender women.

Who is the study for?
This trial is for young Black and/or Latino men who have sex with men and transgender women, aged 15-29, living in the U.S., who've had condomless anal sex with a man in the last 6 months. Participants must have internet access and own or regularly use a smartphone or laptop/tablet.Check my eligibility
What is being tested?
The study tests an online intervention designed to provide social support, HIV testing information, and resources tailored to reduce stigma's impact on HIV outcomes among participants. It's a randomized trial with three groups to compare different approaches.See study design
What are the potential side effects?
Since this trial involves social support and informational resources rather than medical treatments, traditional physical side effects are not expected. However, emotional or psychological responses may vary based on individual experiences.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-month, 6-month, 9-month, and 12-month follow-up assessments
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3-month, 6-month, 9-month, and 12-month follow-up assessments for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in HIV Testing Behavior
Change in Viral Suppression
Secondary outcome measures
Changes in Pre-Exposure Prophylaxis (PrEP) uptake
Changes in Treatment Adherence

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Peer-referred HMP network armExperimental Treatment3 Interventions
Participants randomized to Intervention Arm 2 (peer-created network) will be enrolled into a parallel (but separate) version of HMP 2.0. The only difference between the two intervention arms is that the peer-referred HMP network arm will allow participants to refer and enroll 2 peers of their choosing into the study.
Group II: HMP 2.0 ArmExperimental Treatment3 Interventions
Participants in this experimental arm will receive access to HMP 2.0, an interactive site that includes a Knowledge Center focused on HIV prevention content, interactive forums, and a provider question & answer platform.
Group III: Information-Only ArmActive Control2 Interventions
The HMP 2.0 Information-Only Control Arm will feature a streamlined version of the website that provides tailored information and content for YBLMT. This follows the design of HMP 1.0 where control arm participants had access to HIV-related Knowledge Center articles of the main intervention without access to the engagement features, interactive forums, or doctor Q&A. HIV-negative and sero-unknown participants also will be able to request HIV home test kits. The choice of control arm balances equipoise with research study design; in HMP 1.0, control arm participants also experienced a statistically significant intervention benefit.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Social Support
2022
Completed Phase 2
~3440
HIV Testing
2015
N/A
~860
Information Resources
2020
N/A
~750

Find a Location

Who is running the clinical trial?

University of PennsylvaniaLead Sponsor
2,000 Previous Clinical Trials
42,879,338 Total Patients Enrolled
University of North CarolinaOTHER
166 Previous Clinical Trials
1,448,857 Total Patients Enrolled
Duke UniversityOTHER
2,359 Previous Clinical Trials
3,419,559 Total Patients Enrolled

Media Library

HIV Testing Clinical Trial Eligibility Overview. Trial Name: NCT03678181 — N/A
Human Immunodeficiency Virus Infection Research Study Groups: Information-Only Arm, HMP 2.0 Arm, Peer-referred HMP network arm
Human Immunodeficiency Virus Infection Clinical Trial 2023: HIV Testing Highlights & Side Effects. Trial Name: NCT03678181 — N/A
HIV Testing 2023 Treatment Timeline for Medical Study. Trial Name: NCT03678181 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Am I qualified to participate in this experiment?

"This medical trial seeks to enrol 1050 adolescents and young adults who are HIV-positive, have a Black/African American or Latino/Hispanic ethnicity, U.S residency (verified by zip code), report of at least one occurrence of unprotected anal intercourse in the preceding 6 months, an assigned male sex at birth, identification as either male or female gender identity and possess internet access alongside regular utilisation of a smartphone device or laptop/tablet with which they can log into the study website."

Answered by AI

How many patients are participating in this trial?

"Affirmative, the clinicaltrials.gov website reveals that this medical investigation is recruiting participants with a starting date of July 7th 2020 and an updated version on January 19th 2022. The trial needs 1050 individuals from 3 locations to participate in it."

Answered by AI

Does this research include participants aged 60 and above?

"This medical trial is exclusive to individuals between 15 and 29 years of age. For those younger or older than this range, there are 122 studies available for patients under 18 and 381 trials suitable for people over 65."

Answered by AI

Are there any vacancies in this medical experiment for potential participants?

"Affirmative. The clinical trial is advertised on clinicialtrials.gov and still looking for participants; the listing was first posted in July 2020 and edited lastly in January of 2022, with a total goal to recruit 1050 patients from 3 different sites."

Answered by AI
~158 spots leftby Apr 2025