Study on Stigma and Shame in HIV and Substance Use Disorders
This study is testing an intervention called "Matter Intervention" to help people living with HIV (human immunodeficiency virus) and substance use disorders (SUDs) better manage their health. It aims to reduce the negative effects of stigma and shame, which can make it harder to stay engaged in HIV care and keep the virus under control. You might be able to join if you are HIV-positive, have an SUD (not just tobacco, cannabis, or alcohol), and feel internalized stigma related to HIV, substance use, sexual orientation, or gender identity. You also need to have a detectable viral load or inconsistent medication adherence. The study will compare the Matter Intervention to a control condition that provides information about local resources. The main goal is to see if the Matter Intervention helps people achieve viral suppression (when the amount of HIV in the blood is very low) after 12 months. The study is currently unclear about its recruitment status and plans to enroll 256 participants.
- Study design
- This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 256 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for 12 months to assess viral suppression.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Mitigating the Impact of Stigma and Shame Among People Living With HIV and Substance Use Disorders
At a glance
Conditions
Where it's being run
2 sites across 2 statesStudy leadership
- Abigail Batchelder, PhD, MPH · PRINCIPAL_INVESTIGATOR · CABU School of Medicine, Psychiatry
Who to contact
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Do you actually qualify for this trial?
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Inclusion
What this trial measures
- Viral Suppression at 12 month follow-up12 month follow up
Compare the proportion of participants randomized to the intervention to the proportion of those randomized to the time-matched control condition who are virally suppressed at the 12 months follow up visit.