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Linking Infectious and Narcology Care-Part II (LINC-II)

Primary Purpose

HIV Infection, Drug Use

Status
Completed
Phase
Phase 4
Locations
Russian Federation
Study Type
Interventional
Intervention
Rapid ART initiation
Pharmacotherapy for opioid use disorder
Strengths-based HIV case management
Sponsored by
Boston Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for HIV Infection focused on measuring Russia, Substance use, Peer case managers, ART, HIV

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years or older
  • HIV infected
  • Hospitalized at narcology hospital
  • History of injection drug use
  • Current diagnosis of opioid use disorder
  • Provision of information for 2 contacts to assist with follow-up
  • Address within 100 kilometers of St. Petersburg
  • Possession of a telephone (home or cell)
  • Able and willing to comply with all study protocols and procedures

Exclusion Criteria:

  • Not fluent in Russian
  • Cognitive impairment
  • Pregnancy, planning to become pregnant, or breastfeeding
  • ART use in past 30 days prior to hospitalization
  • Known hypersensitivity to naltrexone
  • Acute severe psychiatric illness (i.e. ,answered yes to any of the following: past three month active hallucinations; mental health symptoms prompting a visit to the ED or hospital; mental health medication changes due to worsening symptoms; presence of suicidal ideations)
  • Known history of liver failure
  • ALT or AST >5 times the upper limit of normal
  • Known severe thrombocytopenia (<50k)
  • Known coagulation disorder/taking anticoagulation medications
  • Body habitus that precludes intramuscular injection
  • Known hypersensitivity to naloxone
  • Known history of Raynaud's disease
  • Known history of Itsenko-Cushing syndrome
  • Known history of generalized mycoses
  • Known history of glaucoma
  • Known history of osteoporosis.
  • Planned surgeries in the next 12 months

Sites / Locations

  • First St. Petersburg Pavlov State Medical University
  • City Addiction Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

LINC-II

Standard of Care

Arm Description

LINC-II is a multi-faceted intervention combining pharmacological therapy (i.e., ART and naltrexone for opioid use disorder) and 12 months of strengths-based case management delivered to coordinate care across the narcology and HIV health care systems.

Participants randomized to the control group will receive the narcology hospital's standard of care, which is detoxification with or without stabilization. Prior to discharge, those identified as HIV-infected are given contact details for an HIV clinic, not an appointment. Upon discharge, patients are encouraged to receive outpatient narcology treatment, monthly, for 1 year. For this study, with regard to linkage to HIV medical care, patients will be given printed information about where to obtain HIV medical care and a resource card containing harm reduction information.

Outcomes

Primary Outcome Measures

Undetectable HIV Viral Load at 12 Months
Number of participants with undetectable HIV viral load at 12 months, assessed by HIV viral load lab test (<40 copies per milliliter)

Secondary Outcome Measures

Initiation of Antiretroviral Therapy (ART)
Number of participants who initiated ART within 28 days of randomization. Data will be extracted from medical record.
Change in Mean CD4 Count From Baseline to 12 Months
The change in the mean CD4 count (CD4 cells per cubic millimeter) will be calculated from the baseline and 12 months lab results
Retention in HIV Care
Number of participants who had at least 1 visit to HIV medical care in 2 consecutive 6 month periods. Data will be extracted from medical record.
Undetectable HIV Viral Load at 6 Months
Number of participants with undetectable HIV viral load at 6 months, assessed by HIV viral load lab test (<40 copies per milliliter).

Full Information

First Posted
September 19, 2017
Last Updated
March 26, 2023
Sponsor
Boston Medical Center
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT03290391
Brief Title
Linking Infectious and Narcology Care-Part II
Acronym
LINC-II
Official Title
Linking Infectious and Narcology Care-Part II
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
September 19, 2018 (Actual)
Primary Completion Date
April 6, 2022 (Actual)
Study Completion Date
April 6, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Boston Medical Center
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study, "Linking Infectious and Narcology Care - Part II (LINC-II)," will implement and evaluate a multi-faceted intervention (LINC-II), via a two-armed randomized controlled trial among 240 HIV-infected PWID in St. Petersburg. LINC-II, comprised of pharmacological therapy (i.e., rapid access to ART and receipt of naltrexone for opioid use disorder) and 12 months of strengths-based case management, will assess HIV outcomes (e.g., HIV viral load suppression), impact on care systems and cost-effectiveness of the intervention.
Detailed Description
Russia and Eastern Europe continue to have one of the fastest growing HIV epidemics in the world, with highest transmission risks among people who inject drugs (PWID) and their sexual partners. While routine HIV testing within addiction treatment systems in Russia (i.e., narcology hospitals) is the norm, links between the narcology and HIV care systems are limited and ineffective. In St. Petersburg 50-60% of PWID are HIV-infected, yet among this population less than 10% are on antiretroviral therapy (ART). For Russia to make progress toward the UNAIDS 90-90-90 targets (i.e., 90% aware of HIV diagnosis, 90% of those diagnosed on ART and 90% of those on ART with suppressed HIV viral load [HVL]), a bold new strategy is required. The objective of this study, "Linking Infectious and Narcology Care - Part II (LINC-II)," is to implement and evaluate, via a two-armed randomized controlled trial among 240 HIV-infected PWID, a multi-faceted intervention combining pharmacological therapy (i.e., rapid access to ART and receipt of naltrexone for opioid use disorder) and 12 months of strengths-based case management. The central hypothesis is that LINC-II will lead to marked progress toward the achievement of the 90-90-90 HIV cascade of care targets among HIV-infected PWID, relative to current standard of care, and that LINC-II will facilitate health system coordination of narcology and HIV care. LINC-II aims to: 1) evaluate the effectiveness of LINC-II on undetectable HVL at 12 months (primary outcome), initiation of ART within 28 days of randomization, change in CD4 count from baseline to 12 months, retention in HIV care (i.e., ≥ 1 visit to medical care in 2 consecutive 6 month periods), and undetectable HVL at 6 months; 2) evaluate the impact of LINC-II on coordinated care across the narcology and HIV health care systems, using mixed methods data from health care providers, administrators, and patients; and 3) evaluate the cost-effectiveness of the intervention to inform policy makers on scaling up the LINC-II approach both within Russia and other countries with HIV epidemics driven by injection drug use.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection, Drug Use
Keywords
Russia, Substance use, Peer case managers, ART, HIV

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
225 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LINC-II
Arm Type
Experimental
Arm Description
LINC-II is a multi-faceted intervention combining pharmacological therapy (i.e., ART and naltrexone for opioid use disorder) and 12 months of strengths-based case management delivered to coordinate care across the narcology and HIV health care systems.
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Participants randomized to the control group will receive the narcology hospital's standard of care, which is detoxification with or without stabilization. Prior to discharge, those identified as HIV-infected are given contact details for an HIV clinic, not an appointment. Upon discharge, patients are encouraged to receive outpatient narcology treatment, monthly, for 1 year. For this study, with regard to linkage to HIV medical care, patients will be given printed information about where to obtain HIV medical care and a resource card containing harm reduction information.
Intervention Type
Other
Intervention Name(s)
Rapid ART initiation
Intervention Description
The infectionist will streamline the approval with the ultimate goal of starting participants on ART while they are still hospitalized at the City Addiction Hospital.
Intervention Type
Drug
Intervention Name(s)
Pharmacotherapy for opioid use disorder
Other Intervention Name(s)
Naltrexone
Intervention Description
Thirteen months of naltrexone treatment for opioid use disorder (injection at baseline, followed by 4 implants).
Intervention Type
Behavioral
Intervention Name(s)
Strengths-based HIV case management
Intervention Description
Strengths-based case management: 10 sessions over 12 months in which a trained case manager (CM) meets individually with patients to motivate them to engage in HIV medical care by supporting the recognition of their own strengths to make positive changes in their lives and ultimately improve their HIV outcomes.
Primary Outcome Measure Information:
Title
Undetectable HIV Viral Load at 12 Months
Description
Number of participants with undetectable HIV viral load at 12 months, assessed by HIV viral load lab test (<40 copies per milliliter)
Time Frame
12 months post randomization
Secondary Outcome Measure Information:
Title
Initiation of Antiretroviral Therapy (ART)
Description
Number of participants who initiated ART within 28 days of randomization. Data will be extracted from medical record.
Time Frame
Within 28 days of randomization
Title
Change in Mean CD4 Count From Baseline to 12 Months
Description
The change in the mean CD4 count (CD4 cells per cubic millimeter) will be calculated from the baseline and 12 months lab results
Time Frame
Change from baseline to 12 months
Title
Retention in HIV Care
Description
Number of participants who had at least 1 visit to HIV medical care in 2 consecutive 6 month periods. Data will be extracted from medical record.
Time Frame
12 months
Title
Undetectable HIV Viral Load at 6 Months
Description
Number of participants with undetectable HIV viral load at 6 months, assessed by HIV viral load lab test (<40 copies per milliliter).
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years or older HIV infected Hospitalized at narcology hospital History of injection drug use Current diagnosis of opioid use disorder Provision of information for 2 contacts to assist with follow-up Address within 100 kilometers of St. Petersburg Possession of a telephone (home or cell) Able and willing to comply with all study protocols and procedures Exclusion Criteria: Not fluent in Russian Cognitive impairment Pregnancy, planning to become pregnant, or breastfeeding ART use in past 30 days prior to hospitalization Known hypersensitivity to naltrexone Acute severe psychiatric illness (i.e. ,answered yes to any of the following: past three month active hallucinations; mental health symptoms prompting a visit to the ED or hospital; mental health medication changes due to worsening symptoms; presence of suicidal ideations) Known history of liver failure ALT or AST >5 times the upper limit of normal Known severe thrombocytopenia (<50k) Known coagulation disorder/taking anticoagulation medications Body habitus that precludes intramuscular injection Known hypersensitivity to naloxone Known history of Raynaud's disease Known history of Itsenko-Cushing syndrome Known history of generalized mycoses Known history of glaucoma Known history of osteoporosis. Planned surgeries in the next 12 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey Samet, MD MA MPH
Organizational Affiliation
Boston University
Official's Role
Principal Investigator
Facility Information:
Facility Name
First St. Petersburg Pavlov State Medical University
City
St. Petersburg
ZIP/Postal Code
197022
Country
Russian Federation
Facility Name
City Addiction Hospital
City
St. Petersburg
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36402082
Citation
Bovell-Ammon BJ, Kimmel SD, Cheng DM, Truong V, Michals A, Vetrova M, Hook K, Idrisov B, Blokhina E, Krupitsky E, Samet JH, Lunze K. Incarceration history, antiretroviral therapy, and stigma: A cross-sectional study of people with HIV who inject drugs in St. Petersburg, Russia. Int J Drug Policy. 2023 Jan;111:103907. doi: 10.1016/j.drugpo.2022.103907. Epub 2022 Nov 17.
Results Reference
derived
PubMed Identifier
31931884
Citation
Gnatienko N, Lioznov D, Raj A, Blokhina E, Rosen S, Cheng DM, Lunze K, Bendiks S, Truong V, Bushara N, Toussova O, Quinn E, Krupitsky E, Samet JH. Design of a randomized controlled trial to Link Infectious and Narcology Care (LINC-II) in St. Petersburg, Russia. Addict Sci Clin Pract. 2020 Jan 13;15(1):1. doi: 10.1186/s13722-020-0179-8.
Results Reference
derived

Learn more about this trial

Linking Infectious and Narcology Care-Part II

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