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NCT07792070Completed

Pilot Study to Evaluate the Decentralization of Patient Care Among People With HIV in Out-of-hospital Settings

Source: ClinicalTrials.gov · Last updated 28 Aug 2026

Brief summary (registry, in English)

The goal of this 24-week, open-label, randomized pilot study is to assess the feasibility and impact of decentralized HIV care in a community setting (BCN Checkpoint), focusing on patient satisfaction and experience and carbon footprint. The main question it aims to answer is patients' satisfaction with the medical care at week 24, derived from decentralizing the patient care compared to continuing with the usual follow-up at the hospital. Participants will attend a medical follow-up visit at week 24, an analytical test visit at week 24, and collect ARV every 8 weeks, at the center assigned during randomization (Hospital or BCN Checkpoint); as well as to fill a series of questionnaires at baseline and week 24.

Status (registry)
Completed
Study type
Interventional
Enrollment
54 (actual)
First submitted
19 Aug 2026
Start date
7 Nov 2024
Primary completion date
20 Jan 2026
Lead sponsor
Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
Diseases
HIV
NCT number
NCT07792070

What you commit to

  • Study type: Interventional
  • Participants enrolled: 54
  • From 7 Nov 2024 to the primary completion date, 20 Jan 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants who are already using the locker system to pick up their medication.

Other illness

  • Acute disease or decompensated chronic diseases in the last 6 months.
  • Any other condition that advises against out-of-hospital follow-up.

Other

  • Pregnant Women

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital Universitario Germans Trias i Pujol
Coordinator of this site? Confirm its status
BadalonaSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.