Could moving HIV care out of hospitals boost satisfaction and cut carbon?
NCT ID NCT07792070
First seen Aug 28, 2026 · Last updated Aug 28, 2026
Summary
This pilot study tests whether people with HIV who receive routine care at a community center, instead of a hospital, feel more satisfied with their care. Researchers will compare satisfaction between two groups: one getting care at the community facility and one continuing usual hospital follow-up. The study also looks at whether community-based care reduces the carbon footprint. Participants will have medical visits, blood tests, and collect their antiretroviral medication every two months over 24 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Decentralization of HIV medical care, including follow-up visits, antiretroviral collection, and analytical tests at a community facility (BCN Checkpoint) instead of a hospital
- What this could lead to
- If this works, community-based HIV care could become a standard option, improving patient satisfaction and reducing the environmental impact of hospital visits.
- What could go wrong
- This is a small pilot study with 54 participants, so results may not apply broadly. Decentralized care might not suit everyone, and satisfaction could vary.
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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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54 people
The number who actually took part.
- Started
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Nov 2024
- Finished
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Jan 2026
- 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: * Stable ARV treatment for ≥6 months with oral medications including: * Biktarvy (bictegravir/emtricitabina/tenofovir alafenamida) * Dovato (dolutegravir/lamivudina) * Juluca (dolutegravir/rilpivirina) * dolutegravir + emtricitabina/tenofovir * Symtuza (darunavir/cobicistat/emtricitabina/tenofovir alafenamida) * Undetectable HIV viral load for ≥6 months. * Good treatment adherence according to the HIV and pharmacy teams. * Good adherence to medical appointments * Using a mobile app and acceptance of the established process. * Signed Informed Consent. Exclusion Criteria: * Acute disease or decompensated chronic diseases in the last 6 months. * Any other condition that advises against out-of-hospital follow-up. * Participants who are already using the locker system to pick up their medication. * Pregnant Women
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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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Hospital Universitario Germans Trias i Pujol
Badalona, Barcelona, 08916, Spain
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