OIT-HCMC: Medication-assisted Treatment for Injecting Drug Users in Vietnam

Sponsor
University of Pennsylvania (Other)
Overall Status
Completed
CT.gov ID
NCT05368675
Collaborator
National Institute of Drug Abuse (U.S. Fed), Expertise France (Other)
448
56.4

Study Details

Study Description

Brief Summary

HIV continues to spread around the world and new infections in Asia are one of the most important areas for prevention among drug using populations. There is strong and consistent evidence from several countries that while injection drug users (IDU) continue to be a source of new infections, treatment of opiate addiction is an effective prevention measure against further spread. The project evaluated the implementation of a comprehensive opioid use disorder treatment program co-located with an HIV clinic in Ho Chi Minh City, Vietnam. The program includes medication for opioid use disorder (methadone, buprenorphine/naloxone), standardized counseling sessions (BDRC) and HIV testing and care (for people living with HIV).

Condition or Disease Intervention/Treatment Phase
  • Drug: medication for opioid use disorder
Phase 4

Detailed Description

The drug treatment and HIV research literature of the past 20 years provides strong support for the ability of drug treatment programs to reduce the frequency of drug use, risk behaviors, and incidence of new infections. Findings from these studies also suggest that drug users living with HIV who remain in medication assisted treatment (MAT) and cease drug use are significantly more likely to achieve sustained viral suppression and consequently less likely to transmit HIV. While these data are strong and consistent, they are all derived from countries with highly developed drug and HIV treatment systems. Little data exist regarding the challenges of implementing and integrating new strategies for MAT with linkages to HIV care in resource-limited settings with developing drug and HIV treatment systems.

The proposed project will take place in Ho Chi Minh City (HCMC), Vietnam. In HCMC, 51.8 % of IDUs are estimated to be HIV positive (HCMC Provincial AIDS Committee (PAC) 2009). Methadone maintenance treatment (MMT) for IDUs started as a pilot program in 2008 in Haiphong and HCMC, two of the highest prevalence provinces for injecting drug use. By December 2009, 784 patients were under MMT and 235 were receiving ARV. 30% of patients under MMT are HIV+ (HCMC PAC, 2009). The National goal is to have 80,000 drug users in methadone treatment by 2015. There are currently no buprenorphine/naloxone treatment programs in Vietnam.

The proposed project evaluate the implementation of an MAT program (both methadone and buprenorphine/naloxone) integrated within an HIV treatment setting. This is the first project to establish and evaluate the implementation a buprenorphine/naloxone (Suboxone) treatment program in Vietnam. Participants were enrolled in the integrated MAT program that included drug and risk counseling, and for those who are living with HIV, HIV treatment. Participant'received care for 12 months and then transitioned to community treatment program. The study assessed barriers to implementation.

Primary measures consisted of facilitators and barriers to implementation and retention in

MAT generally and Suboxone treatment specifically. The following specific aims are evaluated:
  • Establish a new integrated MAT treatment program within and HIV treatment setting in HCMC;

  • Evaluate barriers and facilitators to implementation of integrated MAT/HIV treatment;

  • Evaluate patient retention and medication adherence in integrated MAT/HIV Care;

  • Estimate the costs and benefits of MAT treatment strategies.

Study Design

Study Type:
Interventional
Actual Enrollment :
448 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
A Pilot Implementation Project of Methadone and Suboxone® for Injecting Drug Users in Ho Chi Minh City, Vietnam
Actual Study Start Date :
Dec 18, 2013
Actual Primary Completion Date :
Aug 31, 2017
Actual Study Completion Date :
Aug 31, 2018

Outcome Measures

Primary Outcome Measures

  1. Retention in treatment program at 12 months [12 months]

    Percentage of participants who stay in treatment for 12 months

  2. Adherence in treatment program at 12 months [12 months]

    Missing doses of treatment during time in the study

  3. Cost of 12-month treatment program [12 months]

    Cost of 12 months of the treatment program evaluated with the Drug Abuse Treatment Cost Analysis Program (DATCAP)

Secondary Outcome Measures

  1. Change in substance use from baseline to 12-month follow-up [12 months]

    Evaluation of the change in substance use between baseline and 12-month follow-up assessed by weekly self-report and urine drug screen

  2. Viral load suppression for people living with HIV [12 months]

    Percentage of participants living with HIV with a suppressed viral load at 12 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • • 18 or more years of age

  • Meets DSM-5 criteria for opiate use disorder

  • Positive urine drug screen for heroin or other opiates

  • Interested in methadone maintenance or Suboxone® treatment for opiate use disorder

  • Injected heroin within past 30 days by self-report, documented by "tracks" or puncture marks

  • Willingness and ability to give informed consent and otherwise participate

  • Provision of adequate locator information

Exclusion Criteria:
  • • Clinically significant cognitive impairment, schizophrenia, paranoid disorder, bipolar disorder

  • Known neurological, cardiovascular, renal, or other medical disorder that is likely to impair or make the patient's participation hazardous

  • Physiologically dependent on alcohol, benzodiazepines, or other sedative type drugs

  • Pending legal charges with likely incarceration within next 12 months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Pennsylvania
  • National Institute of Drug Abuse
  • Expertise France

Investigators

  • Principal Investigator: Charles P O'Brien, MD, PhD, University of Pennsylvania

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT05368675
Other Study ID Numbers:
  • R01DA033671
First Posted:
May 10, 2022
Last Update Posted:
May 10, 2022
Last Verified:
May 1, 2022
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 University of Pennsylvania
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 10, 2022