Delivering integrated strategies from a mobile unit to address the intertwining epidemics of HIV and addiction in people who inject drugs: the HPTN 094 randomized controlled trial protocol (the INTEGRA Study).


Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
15 Feb 2024
Historique:
received: 01 07 2023
accepted: 22 12 2023
medline: 16 2 2024
pubmed: 16 2 2024
entrez: 15 2 2024
Statut: epublish

Résumé

Persons with opioid use disorders who inject drugs (PWID) in the United States (US) face multiple and intertwining health risks. These include interference with consistent access, linkage, and retention to health care including medication for opioid use disorder (MOUD), HIV prevention using pre-exposure prophylaxis (PrEP), and testing and treatment for sexually transmitted infections (STIs). Most services, when available, including those that address substance misuse, HIV prevention, and STIs, are often provided in multiple locations that may be difficult to access, which further challenges sustained health for PWID. HPTN 094 (INTEGRA) is a study designed to test the efficacy of an integrated, "whole-person" strategy that provides integrated HIV prevention including antiretroviral therapy (ART), PrEP, MOUD, and STI testing and treatment from a mobile health delivery unit ("mobile unit") with peer navigation compared to peer navigation alone to access these services at brick and mortar locations. HPTN 094 (INTEGRA) is a two-arm, randomized controlled trial in 5 US cities where approximately 400 PWID without HIV are assigned either to an experimental condition that delivers 26 weeks of "one-stop" integrated health services combined with peer navigation and delivered in a mobile unit or to an active control condition using peer navigation only for 26 weeks to the same set of services delivered in community settings. The primary outcomes include being alive and retained in MOUD and PrEP at 26 weeks post-randomization. Secondary outcomes measure the durability of intervention effects at 52 weeks following randomization. This trial responds to a need for evidence on using a "whole-person" strategy for delivering integrated HIV prevention and substance use treatment, while testing the use of a mobile unit that meets out-of-treatment PWID wherever they might be and links them to care systems and/or harm reduction services. Findings will be important in guiding policy for engaging PWID in HIV prevention or care, substance use treatment, and STI testing and treatment by addressing the intertwined epidemics of addiction and HIV among those who have many physical and geographic barriers to access care. ClinicalTrials.gov NCT04804072 . Registered on 18 March 2021.

Sections du résumé

BACKGROUND BACKGROUND
Persons with opioid use disorders who inject drugs (PWID) in the United States (US) face multiple and intertwining health risks. These include interference with consistent access, linkage, and retention to health care including medication for opioid use disorder (MOUD), HIV prevention using pre-exposure prophylaxis (PrEP), and testing and treatment for sexually transmitted infections (STIs). Most services, when available, including those that address substance misuse, HIV prevention, and STIs, are often provided in multiple locations that may be difficult to access, which further challenges sustained health for PWID. HPTN 094 (INTEGRA) is a study designed to test the efficacy of an integrated, "whole-person" strategy that provides integrated HIV prevention including antiretroviral therapy (ART), PrEP, MOUD, and STI testing and treatment from a mobile health delivery unit ("mobile unit") with peer navigation compared to peer navigation alone to access these services at brick and mortar locations.
METHODS METHODS
HPTN 094 (INTEGRA) is a two-arm, randomized controlled trial in 5 US cities where approximately 400 PWID without HIV are assigned either to an experimental condition that delivers 26 weeks of "one-stop" integrated health services combined with peer navigation and delivered in a mobile unit or to an active control condition using peer navigation only for 26 weeks to the same set of services delivered in community settings. The primary outcomes include being alive and retained in MOUD and PrEP at 26 weeks post-randomization. Secondary outcomes measure the durability of intervention effects at 52 weeks following randomization.
DISCUSSION CONCLUSIONS
This trial responds to a need for evidence on using a "whole-person" strategy for delivering integrated HIV prevention and substance use treatment, while testing the use of a mobile unit that meets out-of-treatment PWID wherever they might be and links them to care systems and/or harm reduction services. Findings will be important in guiding policy for engaging PWID in HIV prevention or care, substance use treatment, and STI testing and treatment by addressing the intertwined epidemics of addiction and HIV among those who have many physical and geographic barriers to access care.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov NCT04804072 . Registered on 18 March 2021.

Identifiants

pubmed: 38360750
doi: 10.1186/s13063-023-07899-5
pii: 10.1186/s13063-023-07899-5
doi:

Banques de données

ClinicalTrials.gov
['NCT04804072']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

124

Subventions

Organisme : National Institute of Allergy and Infectious Diseases
ID : UM1AI068619-15
Organisme : National Institute of Allergy and Infectious Diseases
ID : UM1AI068617-15
Organisme : National Institute of Allergy and Infectious Diseases
ID : UM1AI068613-15

Informations de copyright

© 2024. The Author(s).

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Auteurs

David Goodman-Meza (D)

Division of Infectious Diseases, David Geffen School of Medicine, University of California, Los Angeles, 10833 Le Conte Ave., CHS 52-215, Los Angeles, CA, 90095-1688, USA. dgoodman@mednet.ucla.edu.

Steven Shoptaw (S)

Department of Family Medicine, University of California, Los Angeles, Los Angeles, CA, USA.

Brett Hanscom (B)

Statistical Center for HIV/AIDS Research and Prevention (SCHARP), Seattle, WA, USA.

Laramie R Smith (LR)

Division of Infectious Diseases and Global Public Health, University of California, San Diego, San Diego, CA, USA.

Philip Andrew (P)

Family Health International (FHI 360), Durham, NC, USA.

Irene Kuo (I)

Milken Institute School of Public Health Department of Epidemiology, George Washington University, Washington, DC, USA.

Jordan E Lake (JE)

UTHealth-Houston, Houston, TX, USA.

David Metzger (D)

Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Ellen A B Morrison (EAB)

ICAP, Mailman School of Public Health, Columbia University, New York, NY, USA.

Melissa Cummings (M)

Statistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Jessica M Fogel (JM)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Paul Richardson (P)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Jayla Harris (J)

Family Health International (FHI 360), Durham, NC, USA.

Jesse Heitner (J)

Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.

Sarah Stansfield (S)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Nabila El-Bassel (N)

School of Social Work, Columbia University, New York, NY, USA.

Classifications MeSH