A new strategy aims to plug gaps in HIV care for people who inject drugs
NCT ID NCT06025435
First seen Aug 24, 2026 · Last updated Aug 25, 2026 · Updated 1 time
Summary
This trial tests whether a structured improvement strategy, called SAIA, can help syringe service programs in the U.S. deliver more HIV testing and referrals to prevention and treatment services. The study will compare programs using SAIA with those continuing their usual practices over a 21-month period. Researchers will measure changes in HIV testing rates, referrals, and costs to see if the approach is effective and sustainable.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Systems Analysis and Improvement Approach (SAIA) - an organizational strategy to improve HIV service delivery
- What this could lead to
- If effective, this approach could help syringe service programs connect more people who inject drugs to HIV testing, prevention, and treatment, potentially reducing HIV transmission.
- What could go wrong
- This is a small, early-stage implementation study, so results may not generalize widely. The strategy's success depends on staff engagement and resources, and it may not produce lasting improvements.
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 32 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2023
- Expected to finish
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Jun 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 years and older
- 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: * Organization operates within the United States, U.S. territory, or Tribal Nation. * Organization operates a dedicated syringe service program (SSP) that provides access to sterile syringes and injection equipment for people who inject drugs (PWID). * In the past 30 days, SSP staff have directly provided HIV counseling and testing services to SSP participants. Exclusion Criteria: * Organization is participating in or has participated in other studies involving SAIA or components of SAIA. * Organization intends to stop providing HIV counseling and testing services to SSP participants within 21 months of their respective start date.
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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.
Contacts and locations
Locations
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University of California, San Diego
San Diego, California, 92093, United States
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