CHORUS+: Comprehensive HIV, Hepatitis C, and Opioid Use Disorder Response to the Unaddressed Syndemic +

Sponsor
Boston Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05769218
Collaborator
Victory Programs Mobile Prevention Services Van and Navigation Center (Other)
284
2
2
37
142
3.8

Study Details

Study Description

Brief Summary

The US opioid overdose epidemic has been accompanied by an increase in human immunodeficiency (HIV) among persons who inject drugs. HIV pre-exposure prophylaxis (PrEP) is an FDA approved medication taken daily orally by individuals who are HIV negative, but who are at increased risk for HIV. In order to obtain PrEP, a prescription is needed. Before being prescribed HIV PrEP, it is recommended by the Centers for Disease Control and Prevention (CDC) to obtain an HIV test first. Although home HIV self-test kits are recommended by the CDC and are locally available, uptake remains low.

CHORUS+ (Comprehensive HIV, Hepatitis C, and Opioid Use Disorder Response to the Unaddressed Syndemic +) is a theory-based, peer-delivered, mobile phone-supported intervention focused on enhancing uptake and adherence to HIV PrEP (primary outcome), and continuation of MOUD (secondary outcome) among persons who inject opioids. At recruitment, the intervention will include HIV self-testing, rapid initiation of PrEP and MOUD, and 6-month peer recovery coaching (PRC) to support adherence to these medications. This research study seeks to determine the efficacy of a novel intervention to increase the uptake of evidence-based measures to prevent HIV and treat opioid use disorder.

The efficacy of this multi-site, two-arm randomized control trial of CHORUS+ and usual care [passive referral]. This study is not testing the efficacy of PrEP or HIV home testing which is already known. In addition the investigators will determine the influence of HIV self-testing on PrEP uptake and adherence. In the CHORUS+/ intervention arm, there will be a baseline in-person session with the participant to encourage uptake of PrEP and MOUD using motivational interviewing (MI).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: CHORUS+
  • Other: Standard of care
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
284 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
PrEP and MOUD Rapid Access for Persons Who Inject Drugs: the CHORUS+ Study
Anticipated Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2026
Anticipated Study Completion Date :
Jun 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: CHORUS+

The baseline questionnaire for participants in this arm will be followed by a 30-minute motivational interviewing (MI) session with the peer recovery coach (PRC), and will assess readiness for change and provide information about PrEP. The PRC will also assess readiness for MOUD, and this will be further explored during subsequent visits.

Behavioral: CHORUS+
The CHORUS+ intervention will include a baseline interview with a peer recovery coach to encourage uptake of HIV PrEP (pre-exposure prophylaxis) and medications for opioid use disorder (MOUD) through motivational interviewing (MI). Participants will also be offered HIV self-testing on the day of recruitment, HIV PrEP (if they are HIV negative) and MOUD. Participants will then receive peer coaching for 6 months to increase adherence to PrEP and or MOUD.

Active Comparator: Usual care- control

Participants in this arm will receive passive referral for care. there will be no PRC MI session and they will not be offered PrEP or MOUD.

Other: Standard of care
Normal protocols for care of participants who inject opioids will be followed.

Outcome Measures

Primary Outcome Measures

  1. Adherence to HIV PrEP at 6 months Adherence to HIV PrEP [6 months]

    This outcome will be assessed by measured by the proportion of individuals who have dried blood spot tenofovir-diphosphate (TFV-DP) blood level 52.0 ng/ mL or greater at 6 months post-enrollment.

Secondary Outcome Measures

  1. Adherence to PrEP at 3 and 12 months [3 months. 12 months]

    Adherence will be assessed by self-report and chart review of active medication refills for PrEP and appointments attended.

  2. Receipt of medication for opioid use disorder (MOUD) [3 months, 6 months, and 12 months]

    Receipts will be assessed by any of the following: (1) chart review of active medication refills for MOUD, (2) self-report, (3) urine toxicology results checked during study visit, and (4) chart review for appointments attended.

  3. Test results for gonorrhea [Baseline, 3 months, 6 months, and 12 months]

    Results will be assessed as negative or positive.

  4. Test results for chlamydia [Baseline, 3 months, 6 months, and 12 months]

    Results will be assessed as negative or positive.

  5. Test results for syphilis [Baseline, 3 months, 6 months, and 12 months]

    Results will be assessed as negative or positive.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Injected opioids within the past 6 months (by self-report)

  • Willingness to provide contact information for two family members or friends

  • Willingness to sign medical records release forms

  • Ability to speak English

  • Plans to reside in Boston area for the next 6 months

Exclusion Criteria:
  • Individuals with HIV (self report)

  • Express desire to harm themselves or others -

Contacts and Locations

Locations

Site City State Country Postal Code
1 Boston Medical Center Faster Paths Bridge Clinic Boston Massachusetts United States 02118
2 Victory Programs Mobile Prevention Services Van and Navigation Center Boston Massachusetts United States 02118

Sponsors and Collaborators

  • Boston Medical Center
  • Victory Programs Mobile Prevention Services Van and Navigation Center

Investigators

  • Principal Investigator: Sabrina A Assoumou, MD MPH, Boston Medical Center, Infectious Diseases

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Boston Medical Center
ClinicalTrials.gov Identifier:
NCT05769218
Other Study ID Numbers:
  • H-43487
First Posted:
Mar 15, 2023
Last Update Posted:
Mar 15, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Boston Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 15, 2023