grant

Long-acting injectable antiretroviral treatment to improve HIV treatment among justice-involved persons being released to the community

Organization MIRIAM HOSPITALLocation PROVIDENCE, UNITED STATESPosted 30 Sept 2022Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2024AIDSAIDS VirusAcquired Immune DeficiencyAcquired Immune Deficiency SyndromeAcquired Immune Deficiency Syndrome VirusAcquired Immunodeficiency SyndromeAcquired Immunodeficiency Syndrome VirusActive Follow-upAnti-Retroviral AgentsAreaBaltimoreBehavioral ModelClinical TrialsCollaborationsCommunitiesContractorCreativenessDataDevelopmentDisease ProgressionDoseDrugsEligibilityEligibility DeterminationEnvironmentEpidemicFDA approvedFederally Qualified Health CenterFundingFutureGeographyGoalsHIVHIV InfectionsHIV resistanceHIV resistantHTLV-III InfectionsHTLV-III-LAV InfectionsHealthHealthcareHigh PrevalenceHuman Immunodeficiency VirusesHuman T-Lymphotropic Virus Type III InfectionsImprisonmentInjectableInterviewIntramuscular InjectionsJailJusticeLAV-HTLV-IIILymphadenopathy-Associated VirusMarylandMedicalMedicationMental disordersMental health disordersMethodsNational Institutes of HealthOralParticipantPatient RecruitmentsPersonsPharmaceutical PreparationsPilot ProjectsPrisonsProceduresProtocolProtocol ScreeningProtocols documentationProviderPsychiatric DiseasePsychiatric DisorderRandomizedRandomized, Controlled TrialsRegimenRelapseResearchRiskRoleSafetyScheduleServicesSiteSubstance Use DisorderTherapeuticTimeTransmissionTreatment ProtocolsTreatment RegimenTreatment ScheduleTreatment outcomeUnemploymentUnited StatesUnited States National Institutes of HealthUrineViralViral BurdenViral LoadViral Load resultVirus-HIVVulnerable Populationsactive followupanti-retroviralantiretroviral therapyantiretroviral treatmentco-morbidco-morbiditycommunity engagementcommunity re-entrycommunity reentrycomorbiditycreativitydesigndesigningdevelopmentaldrug detectiondrug testingdrug/agentengagement with communitiesexperiencefollow upfollow-upfollowed upfollowuphealth carehigh riskhigh risk grouphigh risk individualhigh risk peoplehigh risk populationhousing instabilityimprovedincarceratedincarcerationinnovateinnovationinnovativeinstably housedintramuscular drug administrationjoblessjoblessnessmental illnessmetropolitanopen labelopen label studyoral HIVout of workparticipant recruitmentpillpilot studypilot testpoor health outcomeprimary outcomepsychiatric illnesspsychological disorderrandomisationrandomizationrandomized control trialrandomly assignedreduced health outcomeresponsesecondary outcomesocial rolesubstance usesubstance use and disordersubstance usersubstance usingtransmission processtreatment adherencetreatment complianceunemployedunstable housingunstably housedviral reboundvirus reboundvulnerable groupvulnerable individualvulnerable peopleworse health outcome
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Full Description

Persons who experience incarceration in the United States are disproportionately impacted by HIV infection and
substance use disorders (SUD) and are at increased risk of having poor health outcomes. The time of release

from carceral settings, known as community re-entry, is a period of particularly high risk for persons with HIV

(PWH). New and creative approaches to sustaining HIV treatment and viral suppression during community re-

entry are urgently needed. Antiretroviral treatment (ART) is highly effective in controlling HIV and can significantly

reduce HIV transmission. However, justice involved PWH often struggle with daily ART adherence during

community re-entry and consequently experience disease progression and contribute to HIV transmission. Long-

acting injectable (LAI) ART is a new alternative to help overcome the challenges of adhering to daily pills. The

first FDA-approved LAI ART regimen, cabotegravir (CAB) and rilpivirine (RPV), is administered by intramuscular

injection every four weeks. There is an immediate opportunity to investigate whether using LAI ART, as opposed

to daily oral ART, has a unique and important role when initiated in carceral settings and continued during

community re-entry with the goal of improving treatment outcomes. We propose a mixed methods study that will

develop and pilot test an LAI ART protocol designed specifically for community re-entry. This study will be

conducted in collaboration with the Maryland Department of Public Safety and Correctional Services, Corizon

Health (state prison medical contractor), and Total Health Care, a Federally Qualified Health Center in the

Baltimore Metropolitan area, an Ending the HIV Epidemic geographic hotspot. Framed by the Behavioral Model

for Vulnerable Populations, our aims include: 1) Conduct interviews with justice and treatment experienced PWH

(n=20), and carceral and community key stakeholders (n=20), to obtain guidance on the development and

implementation of a protocol to transition PWH on oral ART to LAI ART in prison with continuation during

community re-entry. 2) Develop an initial LAI ART community re-entry protocol and conduct an open label pilot

study that will follow 10 incarcerated PWH eligible for LAI ART who are near release from prison for three months

in order to optimize protocol procedures and to pilot study retention methods and assessments. 3) Following

optimization of protocol, conduct a pilot randomized controlled trial among 50 incarcerated PWH eligible for LAI

ART and scheduled to be released from prison; participants will be randomized 1:1 to transition ART to injectable

CAB/RPV or continue daily oral ART regimen through a six-month follow-up period after release. During the

follow-up period, we will assess the primary outcome of HIV viral suppression and secondary outcomes including

continuance of the assigned LAI or oral ART regimen, ART adherence, and substance use. This study will

provide preliminary data to inform the design of a future multi-site fully powered clinical trial that will compare LAI

ART to daily oral ART during community re-entry on sustaining HIV viral suppression after release from prison.

Grant Number: 5R34DA057165-03
NIH Institute/Center: NIH

Principal Investigator: CURT BECKWITH

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