Could popular opinion leaders be the key to HIV prevention?
NCT ID NCT07741474
First seen Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time
Summary
This pilot study tests whether training popular opinion leaders in rural South Africa can increase uptake of HIV prevention tools. Researchers will select and train young adults to share sexual health information and distribute HIV self-tests to their peers. The study will assess feasibility and acceptability through interviews and questionnaires.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Community Popular Opinion Leader (CPOL) training
- What this could lead to
- If successful, this approach could help increase HIV testing and prevention uptake in rural communities, potentially reducing HIV transmission.
- What could go wrong
- This is a small pilot study, so results may not be generalizable. The intervention's success depends on peer leaders' willingness and ability to influence others.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2026
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 to 28 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Resident in Sixhumene study area household Exclusion Criteria: * Unable to 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
1 site. 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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Africa Health Research Institute
uMkhanyakude, KwaZulu-Natal, South Africa
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