Same-Day HIV treatment: a new weapon against stigma?
NCT ID NCT07053514
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
Researchers in Peru are testing whether starting antiretroviral therapy on the same day as diagnosis can reduce the stigma that people with HIV face. The study involves developing a same-day treatment protocol with input from HIV experts, then piloting it with patients and their clinicians. The goal is to see if this approach lowers both patient-reported stigma and provider bias, potentially making HIV care more welcoming.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Same-day antiretroviral therapy (SD-ART) protocol
- What this could lead to
- If successful, this could make starting HIV treatment faster and less stigmatizing, improving care for key affected populations.
- What could go wrong
- This is a small pilot study, so results may not apply broadly. Stigma is complex and may not change with timing alone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 139 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2027
An estimate. Start dates often move.
- Expected to finish
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Oct 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aim 1: HIV experts will be selected from National Societies of HIV experts according to the following criteria: 1) 18 years old or older; 2) Be an HIV expert, including those from NGOs providing HIV care, and international specialists; 3) Provide informed consent. * Aim 2: * NGT Focus Groups (FG) * Staff members 1. 18 years old or older. 2. Be a clinical staff member at Hospital Dos de Mayo or Patrucco Primary Health Center. 3. Provide informed consent. * PWH receiving HIV care 1. 18 years old or older. 2. Identify as member of a KAP. 3. Receive HIV care at Hospital Dos de Mayo or Patrucco Primary Health. 4. Provide informed consent. * PWH who dropped out of HIV care 1. 18 years old or older. 2. Identify as a member of a KAP. 3. Previously received HIV care at Hospital Dos de Mayo or Patrucco Primary Health but dropped out of care, as identified through patient registries. 4. Provide informed consent. * In-depth interviews * 1\) 18 years old or older. * 2\) Be the director of Hospital Dos de Mayo or Patrucco primary health center or the HIV director at the Ministry of Health * 3\) Provide informed consent * Aim 3: * Clinical Staff Dyadic Surveys * 1\) 18 years old or older. * 2\) Be an HIV provider at Hospital Dos de Mayo or Raul Patrucco Primary Health Center. * 3\) Provide HIV care to one of the 125 PWH * 4\) Provide informed consent. * Patient Dyadic Surveys * 1\) 18 years old or older. * 2\) Identify as a member of a KAP. * 3\) Be newly diagnosed with HIV and eligible for SD-ART based on clinical criteria identified from Aims 1 and 2. * 4\) Provide informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centro de Salud Raul Patrucco Puig
Lima, Peru
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Hospital Dos de Mayo
Lima, Peru
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