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Expanded HIV Care in Opioid Substitution Treatment (EHOST) Trial (EHOST)

Primary Purpose

Opioid Use Disorder, HIV

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Expanded HIV care in Opioid Substitution Treatment
Sponsored by
Simon Fraser University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Opioid Use Disorder focused on measuring Cost-effectiveness, Opioid substitution treatment, Integrated care, HIV, HAART, Testing, Linkage to care, Treatment adherence

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Drug treatment clinic currently admitting patients for the treatment of opioid dependence across the province of British Columbia

Exclusion Criteria:

  • Private office-based setting

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Other

    Other

    Other

    Arm Label

    Cluster 1

    Cluster 2

    Cluster 3

    Arm Description

    Cluster 1 is the first OST cluster (with an estimated 15-16 OST sites) to receive the 'Expanded HIV care in Opioid Substitution Treatment' intervention, to be administered during the sixth month of the trial. Cluster 1 will be a 'no intervention' arm in the first 6 months of the study, and will cross-over to an experimental arm for months 6-24.

    Cluster 2 is the second OST cluster (with an estimated 15-16 OST sites) to receive the 'Expanded HIV care in Opioid Substitution Treatment' intervention, to be administered during the twelfth month of the trial. Cluster 2 will be a 'no intervention' arm in the first 12 months of the study, and will cross-over to a experimental arm for month 12-24.

    Cluster 3 is the final OST cluster (with an estimated 15-16 OST sites) to receive the 'Expanded HIV care in Opioid Substitution Treatment' intervention, to be administered during the 18th month of the trial. As such, Cluster 3 will be a 'no intervention' arm in the first 18 months of the study, and will cross-over to an experimental arm for months 18-24.

    Outcomes

    Primary Outcome Measures

    The HIV testing rate among those not known to be HIV positive
    The rate of Highly Active Antiretroviral (HAART) initiation among those not on HAART
    The rate of HAART adherence among those on HAART

    Secondary Outcome Measures

    Full Information

    First Posted
    March 24, 2015
    Last Updated
    April 24, 2017
    Sponsor
    Simon Fraser University
    Collaborators
    BC Centre for Excellence in HIV/AIDS
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02440256
    Brief Title
    Expanded HIV Care in Opioid Substitution Treatment (EHOST) Trial
    Acronym
    EHOST
    Official Title
    The Expanded HIV Care in Opioid Substitution Treatment (EHOST) Stepped-wedge, Cluster-randomized Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2015 (Actual)
    Primary Completion Date
    March 2017 (Actual)
    Study Completion Date
    March 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Simon Fraser University
    Collaborators
    BC Centre for Excellence in HIV/AIDS

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Opioid Substitution Treatment (OST) provides a critical opportunity for HIV testing and linkage to antiretroviral treatment. The EHOST study will evaluate a prescriber-focused intervention to increase HIV testing rates, and optimize antiretroviral treatment, re-engagement and retention outcomes among individuals engaged in OST. 46 OST sites in British Columbia will be randomly allocated into three clusters. Clusters will initiative the intervention at different time points, or steps, with every cluster receiving the intervention.
    Detailed Description
    The public health response to the HIV/AIDS epidemic has turned its focus on means of optimizing health care delivery, and re-engineering delivery systems to maximize case identification, as well as access and sustained engagement in antiretroviral treatment. Opioid Substitution Treatment (OST) provides a critical opportunity for HIV testing and linkage to antiretroviral treatment. The EHOST study is a cluster-randomized, stepped-wedge trial to evaluate a prescriber-focused intervention to increase HIV testing rates, and optimize antiretroviral treatment re-engagement and retention outcomes among individuals engaged in OST. The study will encompass all drug treatment clinics currently admitting patients for the treatment of opioid dependence across the province of British Columbia, which are thought to treat 90% of the OST caseload. The trial will be executed over a 24-month period, with groups of clinics receiving the intervention in 6-month intervals. Evaluation of the effectiveness of the proposed intervention will be conducted entirely through existing data collection mechanisms, and focuses on three primary outcomes: (i) the HIV testing rate among those not known to be HIV positive; (ii) the rate of Highly Active Antiretroviral (HAART) initiation among those not on HAART; and (iii) the rate of HAART continuation among those on HAART. Despite the randomized delivery of the intervention, a difference-in-differences analytical framework will be applied to adjust for potential residual heterogeneity in patient case mix, volume, and quality of care across OST clinics. Facilitated by established collaborations between key stakeholders across the province, we hypothesize that the EHOST intervention will optimize HIV testing and care within this marginalized and hard-to-reach population.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Opioid Use Disorder, HIV
    Keywords
    Cost-effectiveness, Opioid substitution treatment, Integrated care, HIV, HAART, Testing, Linkage to care, Treatment adherence

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    49 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Cluster 1
    Arm Type
    Other
    Arm Description
    Cluster 1 is the first OST cluster (with an estimated 15-16 OST sites) to receive the 'Expanded HIV care in Opioid Substitution Treatment' intervention, to be administered during the sixth month of the trial. Cluster 1 will be a 'no intervention' arm in the first 6 months of the study, and will cross-over to an experimental arm for months 6-24.
    Arm Title
    Cluster 2
    Arm Type
    Other
    Arm Description
    Cluster 2 is the second OST cluster (with an estimated 15-16 OST sites) to receive the 'Expanded HIV care in Opioid Substitution Treatment' intervention, to be administered during the twelfth month of the trial. Cluster 2 will be a 'no intervention' arm in the first 12 months of the study, and will cross-over to a experimental arm for month 12-24.
    Arm Title
    Cluster 3
    Arm Type
    Other
    Arm Description
    Cluster 3 is the final OST cluster (with an estimated 15-16 OST sites) to receive the 'Expanded HIV care in Opioid Substitution Treatment' intervention, to be administered during the 18th month of the trial. As such, Cluster 3 will be a 'no intervention' arm in the first 18 months of the study, and will cross-over to an experimental arm for months 18-24.
    Intervention Type
    Other
    Intervention Name(s)
    Expanded HIV care in Opioid Substitution Treatment
    Intervention Description
    The EHOST intervention entails in-person presentations and consultation sessions with individual OST sites that will: (i) provide rationale for the study (ii) outline action items of the intervention; and (iii) describe guidelines around HIV testing and care. The EHOST intervention will be delivered at three distinct times: (i) at point of OST entry; (ii) following 7 days non-adherence; and (iii) at bi-annual intervals. The interventions are comprised of HIV test offers for individuals of unknown HIV status; offers of HIV-related care, including cluster of differentiation 4 (CD4), plasma viral load (pVL) and resistance tests, along with HAART initiation for those known to be HIV-positive, not on HAART; and regular monitoring for those known to be HIV positive, on HAART.
    Primary Outcome Measure Information:
    Title
    The HIV testing rate among those not known to be HIV positive
    Time Frame
    24 months
    Title
    The rate of Highly Active Antiretroviral (HAART) initiation among those not on HAART
    Time Frame
    24 months
    Title
    The rate of HAART adherence among those on HAART
    Time Frame
    24 months

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Drug treatment clinic currently admitting patients for the treatment of opioid dependence across the province of British Columbia Exclusion Criteria: Private office-based setting
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Bohdan Nosyk, PhD
    Organizational Affiliation
    Simon Fraser University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Expanded HIV Care in Opioid Substitution Treatment (EHOST) Trial

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