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NCT06900829Toboroz

#AWARE.HIV Europe: Supporting Healthcare Professionals to Find Undiagnosed HIV in European Hospitals: An Effectiveness-implementation Trial.

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. márc. 12.

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Rövid összefoglaló (regiszter, angolul)

The #aware.hiv Europe study is a real-world, multicenter, stepped-wedge cluster randomized, effectiveness-implementation trial designed to evaluate whether the introduction of dedicated HIV teams in hospitals can improve HIV testing rates among patients presenting with HIV indicator conditions across ten European countries. Study Design: The study employs a stepped-wedge design, whereby clusters of hospitals transition sequentially from a control phase (routine care) to an intervention phase. All patient data are collected retrospectively from routine care, while prospective data are gathered at the healthcare professional level. The project spans four years and involves hospitals from the Netherlands, Belgium, United Kingdom, Germany, Spain, France, Italy, Romania, Poland, and Ukraine. This design allows for comparison of HIV testing rates and related outcomes before and after the implementation across different settings and time points. Intervention: The core intervention involves the establishment of hospital-based HIV teams. Each team is led by an HIV specialist and supported by nurses and data collectors. Their responsibilities include: Identification and Surveillance: Screening routine electronic health records for HIV indicator conditions using predefined ICD-10 codes and verifying cases that warrant HIV testing. Audit \& Feedback: Providing targeted recommendations to treating physicians when an HIV test is indicated but has not been performed, thereby prompting action. Education \& Training: Delivering training sessions to healthcare professionals to improve their knowledge and attitudes towards HIV testing, prevention, and care. Enabling Environment: Implementing digital solutions and other support mechanisms to streamline testing processes, reduce stigma, and enhance overall guideline adherence. Linkage to prevention: Improving linkage to the locally available preventive services. The intervention is intended to integrate seamlessly into routine hospital care, thereby reinforcing existing guidelines while addressing the current diagnostic testing gap. Endpoints and Outcome Measures: Primary Endpoint: The change in HIV testing rate among patients diagnosed with HIV indicator conditions before and after the implementation of HIV teams. Key Secondary Endpoints: The change in the incidence of new HIV diagnoses among patients with HIV indicator conditions. Variations in HIV testing rates across different countries, medical specialties, and types of indicator conditions, as well as over time. Assessment of the cascade of HIV diagnosis, including the proportion of patients identified with an indicator condition, the offer and acceptance of HIV testing, and documented reasons for non-testing. Evaluation of the cascade of HIV care and prevention, including linkage to HIV care, achievement of viral suppression, and referral and uptake of preventive services. Changes in healthcare professionals' knowledge, attitudes, and levels of stigma towards HIV. Implementation outcomes such as fidelity of HIV team activities, resource utilization, cost-effectiveness, and sustainability of the intervention. Analysis of contextual factors, barriers, and facilitators impacting the implementation process, using established frameworks like CFIR and RE-AIM. Impact: By introducing HIV teams and systematically monitoring their effect on HIV testing practices, the study aims to enhance early HIV diagnosis and improve patient outcomes. The findings will contribute to evidence-based guidelines and may promote the adoption of similar interventions across European healthcare settings, ultimately reducing HIV-associated morbidity, mortality, and transmission rates. This project not only addresses a critical diagnostic gap in HIV care but also provides valuable insights into the effective implementation of complex interventions in routine clinical practice.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
5200 (tervezett)
Első benyújtás
2025. febr. 24.
Kezdés
2025. okt. 1.
Elsődleges befejezés
2029. ápr. 1.
Fő szponzor
Casper Rokx
Betegségek
HIV-fertőzés
NCT-szám
NCT06900829

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 5200
  • 2025. okt. 1. és az elsődleges befejezés (2029. ápr. 1.) között
  • 28 helyszín, 10 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

Ki nem vehet részt

Szó szerint a(z) ClinicalTrials.gov forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.

Egyéb

  • Any hospital that does not meet the inclusion criteria will be excluded from participation. We will not use data of patients who have objected against the use of their data for research.

Kiket keres a vizsgálat

  • Standard of care: HIV testing for HIV indicator conditions should be part of routine care in the country, and any prevailing guidelines on HIV testing and prevention policies can be integrated.
  • Management approval: Hospital management must be willing to allocate resources and provide authorization for the proposed activities, including Surveillance, Audit \& Feedback, Education \& Training, Linkage to Prevention, and fostering an Enabling Environment, including stigma reduction.
  • Resources: Assembling an HIV team led by a local HIV expert should be viable considering the available human resources.
  • Data collection: There should be an IT specialist and IT infrastructure capable of flagging a pre-defined set of HIV indicator conditions and monitoring the project's implementation effects with feedback loops to healthcare professionals.
  • Quality assurance: Continuous linkage for care and access to antiretroviral therapy must be assured.
  • Ethics and Regulatory Compliance: Provision for ethical and regulatory compliance is necessary.

A regiszterben nem jelölt feltételek

  • Since this study involves screening individuals presenting to a specific hospital through a hospital-wide intervention, the inclusion and exclusion criteria are established at the hospital level.

Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket is fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (28)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
University Hospital GhentGhentBelgiumToborzás még nem indult
St. Joseph Krankenhaus Berlin TempelhofBerlinNémetországToboroz
Charité Universitätsmedizin BerlinBerlinNémetországToboroz
Cologne University HospitalCologneNémetországToboroz
Klinikum der Technischen Universität München (TUM)MünchenNémetországToboroz
Hospital Universitario La Paz - Carlos IIIMadridSpanyolországToboroz
La PrincesaMadridSpanyolországToboroz
Infanta LeonorMadridSpanyolországToboroz
European hospital of MarseilleMarseilleFranciaországToboroz
Buckinghamshire Healthcare NHS TrustAylesburyEgyesült KirályságToboroz
Royal Free LondonLondonEgyesült KirályságToboroz
Ospedale San Raffaele S.r.l.MilanOlaszországToboroz
L'Istituto Nazionale per le Malattie Infettive "L. Spallanzani" IRCCSRomaOlaszországToboroz
Rijnstate ZiekenhuisArnhemHollandiaToboroz
Stichting Catharina ZiekenhuisEindhovenHollandiaToboroz
University Medical Center GroningenGroningenHollandiaToboroz
Stichting Maasstad ZiekenhuisRotterdamHollandiaToboroz
Haga ZiekenhuisThe HagueHollandiaToboroz
SPZZOZ Janów LubelskiJanów LubelskiLengyelországToboroz
Wojewodzki Szpital ZespolonyKielceLengyelországToboroz
Państwowy Instytut Medyczny MSWiA w WarszawieWarsawLengyelországToboroz
National Institute for Infectious Diseases "Prof. Dr. Matei Bals"BucharestRomániaToboroz
Fundeni Clinical InstituteBucharestRomániaToboroz
Clinical Emergency Hospital "Prof. Dr. Agrippa Ionescu"BucharestRomániaToboroz
Spitalul Universitar de Urgență BucureștiBucharestRomániaToboroz
Central Military Emergency University Hospital "Dr. Carol Davila"BucharestRomániaToboroz
Central city clinical hospital of Ivano-Frankivsk city councilIvano-FrankivskUkrajnaToboroz
Lviv National Medical UniversityLvivUkrajnaToboroz

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