Providing PrEP, Hepatitis C Treatment, and MOUD Through Telemedicine at Greensboro SSP

Hiv Clinical Trial

— PARTNERUP  

Official title:

Providing A Resource: Telemedicine at Needle Exchanges to Reach Under-served Populations - Greensboro

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05108935
• Other study ID #: Pro00104147_1
• Secondary ID: 5P30AI064518-17
• Status: Completed
• Phase: N/A
• Start date: February 17, 2022
• Est. completion date: March 30, 2023

Study information

• Verified date: January 2023
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to provide medication for opioid use disorder (MOUD) with buprenorphine and naloxone, or bup/nx, pre-exposure prophylaxis (PrEP) for HIV prevention, and/or hepatitis C treatment for persons who inject opioids accessing syringe services programs (SSPs), as part of a comprehensive harm reduction program, and assess the acceptability and feasibility of using telemedicine to implement the program. The initial visit will be conducted in person or remotely via telemedicine given COVID-19 protocols at the SSP site in Greensboro, North Carolina (NC); follow-up visits will be conducted via telemedicine.

Description:

The purpose of this study is to provide medication for opioid use disorder (MOUD) with buprenorphine and naloxone, or bup/nx, pre-exposure prophylaxis (PrEP) for HIV prevention and/or hepatitis C treatment for persons who inject opioids accessing syringe services programs (SSPs), as part of a comprehensive harm reduction program, and assess the acceptability and feasibility of using telemedicine to implement the program. The study objectives are the following: To assess uptake and persistence to bup/nx, PrEP, and hepatitis C treatment as part of a comprehensive telemedicine-based harm reduction program among people who inject drugs using SSPs. To assess feasibility and acceptability of implementing a telemedicine-based care harm reduction program among program implementers To assess feasibility and acceptability of participating in a telemedicine-based harm reduction program among users The study population is people who inject drugs, specifically opioids, and who access services at an SSP in Greensboro, NC. The study team will enroll 30 people who inject drugs accessing the participating SSP. Participants will be enrolled in the study for 6 months. At the end of the study, they will be referred to MOUD and PrEP providers identified in the community. Data collection Enrollment visit: The study coordinator will administer a baseline survey to collect demographics, HIV risk behaviors, and substance use history. Participants will undergo laboratory testing at the SSP to determine eligibility and enrolled participants will be prescribed bup/nx and PrEP free of charge. Follow up visits: Follow-up visits will be conducted via telemedicine at the SSP. Participants on any combination of treatment including MOUD: For the first month (Month 1), telemedicine visits will be weekly with each to ensure that participants are stable on the appropriate bup/nx dose. Starting at Month 2, the telemedicine visits will take place monthly. For participants on any combination of treatment NOT including MOUD: Participants will attend telemedicine follow up visits at month 3 and month 6 to check in and provide labs. All participants will be asked to complete a questionnaire at Month 3 and Month 6 which include questions on HIV risk and drug use, as well as adherence evaluation. All participants will also be asked to participate in qualitative interviews on their experiences with the program at month 1 and month 6. By the end of the study, we hope to determine the following: 1. The proportion of persons who demonstrate no or minimal opioid use 1a. Defined as completing Month 3 and Month 6 visits with self-reported opioid use on ≤4 days in the past month and/or 2 2. The proportion of persons who remain HIV negative. 2a.Measured via negative HIV test at Month 3 and Month 6 3. Among participants who undergo hepatitis C treatment, the hepatitis C cure rate 4. Retention or persistence in care 4a. Defined as the proportion who remain on treatment (all or any combination of MOUD, PrEP, and hepatitis C treatment) at Month 3 and Month 6 4b. We will also examine whether participants are more apt to remain on paired/combined therapy compared to individual treatment. 5. Organizational facilitators and barriers to establishing a telehealth program in an SSP 5a. We will iteratively collect programmatic data and document challenges and problem-solving that occurs throughout the implementation period of providing bup/nx, PrEP, and/or hepatitis C treatment. We will identify and describe organizational factors using the framework of the Implementation Research Logic Model. 6. Patient perspectives on telehealth delivery of PrEP, MOUD, and/or hepatitis C treatment via SSP 6a. Analysis of interview data at Month 1 and Month 6 to measure attitudes toward PrEP, MOUD, and hepatitis C treatment in general, and on delivery of treatment via telehealth and at the SSP 6b. Analysis of questionnaire data at baseline, Month 3, and Month 6

Recruitment information / eligibility

• Status: Completed
• Enrollment: 17
• Est. completion date: March 30, 2023
• Est. primary completion date: March 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years or older
• Participant in SSP
• History of self-report injection opioid use in the past 6 months
• Willing to take bup/nx, PrEP, and/or hepatitis C treatment for 6 months
• Not currently taking PrEP
• HIV negative
• Not pregnant
• Either a history of sharing injection or drug preparation equipment or risk of sexual acquisition of HIV* in the past 6 months *Individuals are considered at risk of sexual acquisition of HIV if they answer yes to any of the items in the below question: In the last 6 months, have any of the following applied to you?
• Traded sex for money or drugs
• Had a sexual partner who is HIV positive
• Did not consistently use condoms when having sex
• Had a bacterial sexually transmitted infections (like gonorrhea, chlamydia, or syphilis)
• No medical contraindications for these medications such as history of renal failure or bone diseases

Exclusion Criteria:

• Have altered mental status in which participant cannot sign a consent form
• Receive a positive pregnancy test (will be checked at screening visit)
• Receive a positive HIV test at enrollment (will be checked at screening visit)
• Have evidence of renal failure (will be checked at screening visit)
• Have a history of hepatitis B (will be checked at screening visit)
• Becoming incarcerated during the study Additional considerations: The following are not exclusion criteria for the study overall, but will affect which

treatment(s) they can receive:

• Are currently receiving some form of MOUD (buprenorphine, naltrexone, methadone) - this makes them ineligible for MOUD treatment through the study, but they can still receive PrEP and/or hepatitis C treatment
• Have received treatment for hepatitis C prior to enrollment - this makes them ineligible for hepatitis C treatment through study, but they can still receive PrEP and/or MOUD

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis A
• Hepatitis C
• Hiv
• Opioid Use
• Opioid Use Disorder
• Opioid-Related Disorders
• Risk Reduction

Intervention

Drug:
• Suboxone
Enrolled participants will be prescribed PrEP Mavyret and/or Suboxone. Follow up visits will be conducted by telemedicine. We are testing whether telemedicine is a feasible method for follow up.
• Truvada
Enrolled participants will be prescribed PrEP Mavyret and/or Suboxone. Follow up visits will be conducted by telemedicine. We are testing whether telemedicine is a feasible method for follow up.
• Mavyret
Enrolled participants will be prescribed PrEP Mavyret and/or Suboxone. Follow up visits will be conducted by telemedicine. We are testing whether telemedicine is a feasible method for follow up.

Locations

Country	Name	City	State
United States	Duke Department of Population Health Sciences	Durham	North Carolina
United States	NC Survivors Union	Greensboro	North Carolina

Sponsors (3)

Lead Sponsor	Collaborator
Duke University	Center for AIDS Research (CFAR), National Institute of Allergy and Infectious Diseases (NIAID)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion who demonstrate no or minimal opioid use.	Defined as self-reported opioid use on =4 days in the past month and/or 2 or more consecutive negative urine tests.	3 months
Primary	Proportion who demonstrate no or minimal opioid use.	Defined as self-reported opioid use on =4 days in the past month and/or 2 or more consecutive negative urine tests.	6 months
Primary	Proportion who remain HIV negative.	Measured via negative HIV test.	3 months
Primary	Proportion who remain HIV negative.	Measured via negative HIV test.	6 months
Primary	Among participants who undergo hepatitis C treatment, the hepatitis C cure rate	Measured via negative hepatitis C test.	6 months
Primary	Persistence in care	Defined as the proportion who remain on treatment.	3 months
Primary	Persistence in care	Defined as the proportion who remain on treatment.	6 months
Primary	Ease/difficulty of visiting a SSP to meet with a provider via telemedicine	Exploratory method, conducted in the form of individual interviews to document the personal experiences of each participant (qualitative method)	month 1
Primary	Ease/difficulty of visiting a SSP to meet with a provider via telemedicine	Exploratory method, conducted in the form of individual interviews to document the personal experiences of each participant (qualitative method)	month 6
Primary	Ease/difficulty of accessing the telemedicine video platform	Exploratory method, conducted in the form of individual interviews to document the personal experiences of each participant (qualitative method)	month 1
Primary	Acceptability of medical care via a telemedicine video platform	Exploratory method, conducted in the form of individual interviews to document the personal experiences of each participant (qualitative method)	6 month
Primary	Participant satisfaction with the program	Exploratory method, conducted in the form of individual interviews to document the personal experiences and opinions of each participant (qualitative method)	1 month
Primary	Participant satisfaction with the program	Exploratory method, conducted in the form of individual interviews to document the personal experiences and opinions of each participant over time (qualitative method)	month 6
Primary	Participant perceived usefulness of the program	Exploratory method, conducted in the form of individual interviews to document the personal experiences and opinions of each participant (qualitative method)	month 1
Primary	Participant perceived usefulness of the program	Exploratory method, conducted in the form of individual interviews to document the personal experiences and opinions of each participant (qualitative method)	month 6
Primary	Motivators and barriers affecting program persistence	Exploratory method, conducted in the form of individual interviews to document the personal experiences and opinions of each participant over time (qualitative method)	month 6
Primary	Motivators and barriers affecting medication adherence and persistence	Exploratory method, conducted in the form of individual interviews to document the personal experiences and opinions of each participant over time (qualitative method)	6 months