Can telehealth bring HIV prevention to rural drug users?
NCT ID NCT06845774
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests whether offering HIV prevention medication (PrEP) through telehealth visits at local health departments helps more people who inject drugs start and stay on PrEP compared to standard education and referrals. Eighty participants in rural Appalachia will be randomly assigned to either the telehealth program or standard care. The goal is to see if removing travel and provider barriers can increase PrEP use in this underserved group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- TelePrEP (telehealth-based PrEP care)
- What this could lead to
- If successful, this approach could make HIV prevention more accessible for people who inject drugs in rural areas, reducing new infections.
- What could go wrong
- This is a small pilot study with only 80 participants, so results may not apply broadly. Telehealth may not overcome all barriers to PrEP adherence.
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 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Jan 2027
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 99 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.
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: * be at least 18 years of age * report at least one occasion of injection drug use in the past month * report an indication for PrEP in the past six months consistent with CDC guidelines for PrEP care * be a documented client of the county health department-based SSP at the time of study entry * express willingness to participate in a multi-session intervention and follow-up Exclusion Criteria: * HIV-positive status * current PrEP care.
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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University of Kentucky
Lexington, Kentucky, 40536, United States
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Other studies related to the condition(s) this trial covers.
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