A comparative effectiveness trial of extended release naltrexone versus extended-release buprenorphine with individuals leaving jail
A comparative effectiveness trial of extended release naltrexone versus extended-release buprenorphine with individuals leaving jail
批准号:
10160255
负责人:
Michael Scott Gordon
金额:
$16.54万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-07-15 至 2024-04-30
关键词:
AIDS/HIV problemAdherenceAdministratorAdverse eventAgonistAreaAwardBuprenorphineClinicalCommunitiesContinuity of Patient CareCountyCrimeCriminal JusticeDeath RateDrug usageEffectivenessEnsureEpidemicEventFDA approvedFormulationFundingGenderHIV riskHealth PersonnelHealth systemImprisonmentIndividualInfectionInjectableInjectionsInterventionIntramuscularJailLearningLettersLiteratureMarylandMental HealthMethadoneNaltrexoneNeedlesOpiate AddictionOpioidOpioid agonistOverdosePatient Self-ReportPharmaceutical PreparationsPharmacotherapyPhasePopulationPreventionPrisonerPrisonsPublic HealthQuality of lifeRandomizedRandomized Clinical TrialsRandomized Controlled TrialsRegulationRelapseResearch DesignRisk BehaviorsSafetySex BehaviorSiteSubcutaneous InjectionsSupervisionTest ResultUrineWomanacceptability and feasibilityarmcomparative effectiveness trialcostdisorder later incidence preventioneconomic valueeffectiveness evaluationeffectiveness implementation studyeffectiveness implementation trialheroin useillicit opioidimplementation facilitationinnovationmedication compliancemenopioid useopioid use disorderopioid withdrawaloverdose deathphysical conditioningpreferenceprescription opioidprescription opioid misuseprimary outcomeprogramsrandomized trialreduced substance userisk minimizationscale upsecondary outcometreatment program
中文摘要
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英文摘要
Abstract
The proposed study is a Type 1 hybrid effectiveness-implementation trial. Early adopters from
the Maryland extended-release naltrexone (XR-NTX) initiative and additional counties who are
willing to provide CAM2038, a new extended-release-buprenorphine (XR-B) formulation will
participate in a randomized controlled trial conducted in 7 counties (10 jails) throughout the state
of Maryland, in which 240 incarcerated men and women will be randomly assigned within
gender within jail to one of two groups: Arm 1. XR-B (n=120). XR-B in jail followed by 6 monthly
injections post-release at a community treatment program. Arm 2. XR-NTX (n=120). One
injection of XR-NTX in jail, followed by 6 monthly injections post-release at a community
treatment program. Aim 1. To determine the effectiveness of XR-B compared to XR-NTX in
terms of: Primary. (a) pharmacotherapy adherence (number of monthly injections received).
Secondary. (b) illicit opioid urine test results; (c) self-reported illicit opioid use; (d) overdose
events (non-fatal and fatal); (e) quality of life (i. physical health; ii. mental health); (f) HIV risk
behaviors (i. sexual behavior; ii. needle use or sharing); and (g) criminal activity (i. crime days; ii.
re-arrest; iii. re-incarceration). Aim 2. To use a learning collaborative involving all 7 RCT county
jurisdictions as well as 3 additional counties that selected not to participate in the randomized
trial to understand factors related to: (a) acceptability of providing long-acting agonists and
antagonists in jail settings; and (b) feasibility of providing medication continuity of care from jail
to community treatment providers. Aim 3. Calculate the cost to the correctional health system of
implementing an XR-B or XR-NTX program, and determine the relative value of each strategy,
including the costs associated with the subsequent interventions in the community, from a state-
policymaker and societal perspective.
The proposed study is innovative because it would be the first randomized clinical trial in the US
assessing effectiveness of receiving XR-B vs. XR-NTX in county jails. The public health impact
of the study will be highly significant and far-reaching because most individuals with OUD do not
receive treatment while incarcerated, thereby substantially raising their likelihood of relapse to
drug use, overdose death, HIV/AIDS infection, and re-incarceration. Finally, understanding how
to expand acceptance of medications for opioid use disorder in jails, particularly long-acting
medications, has far-reaching implications for treatment expansion in this population.
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会议论文
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依托单位:
海外基金