Assessing Long-term CTN 0049 Outcomes, HCV Prevalence and Progression Along the HCV Care Continuum Among HIV/HCV Co-infected Substance Users in the U.S.

HIV Clinical Trial

— CTN 0064  

Official title:

CTN 0064: Assessing Long-term CTN 0049 Outcomes, HCV Prevalence and Progression Along the HCV Care Continuum Among HIV/HCV Co-infected Substance Users in the U.S.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02641158
• Other study ID #: AAAP8757
• Secondary ID: U10DA013720
• Status: Completed
• Phase: N/A
• Start date: December 2015
• Est. completion date: May 9, 2018

Study information

• Verified date: July 2020
• Source: Columbia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Primary Objective: This study will evaluate the effectiveness of an HCV Care Facilitation intervention in moving HIV/HCV co-infected substance users forward along the HCV care continuum (compared with a Control group).

Primary Hypothesis: The number of steps achieved along the HCV care continuum will differ between the two study groups over the 14-month follow-up period.

Secondary Objectives:

Component 1 (Long-term CTN 0049 follow-up):

Using the CTN 0064 baseline data (self-report, medical record abstraction and biological data), the following CTN 0049 primary and secondary outcomes in participants who consented to the CTN 0064 protocol will be re-analyzed to evaluate latent and/or enduring effects of the CTN 0049 interventions:

1. HIV virological suppression

2. HIV primary care visit attendance

3. All-cause mortality

Description:

The CTN 0064 study leverages the existing research infrastructure and cohort of the CTN 0049 (NCT01612169) randomized, controlled trial (RCT). CTN 0049 ("Project HOPE -- Hospital Visit as Opportunity for Prevention and Engagement for HIV-Infected Drug Users") is a three-group RCT that evaluated the most effective strategy to achieve HIV virologic suppression among HIV-infected substance users who were recruited from hospital settings. Between July 2012 and January 2014, a total of 801 HIV-infected hospitalized patients were recruited from 11 participating sites throughout the U.S. and randomized to one of the following three groups: 1) Patient Navigator intervention, 2) Patient Navigator plus Contingency Management intervention, and 3) Treatment as Usual. All CTN 0049 participants provided informed consent and completed baseline computer assisted personal interviews or CAPI (computer assisted personal interview: focusing on drug use, mental health, demographics and socio-economic factors, HIV care and drug treatment history) and blood draws (for HIV viral load and CD4 count). The two intervention groups received up to 11 patient navigation sessions over a 6-month period to actively assist participants in linking to HIV primary care and substance use treatment. Participants in all three groups completed follow-up assessments consisting of CAPI, blood draws, urine collection and breath analysis at approximately 6 and 12 months post-randomization. Medical records were reviewed to document receipt of HIV care and treatment during the study period. CTN 0064 will leverage the CTN 0049 research infrastructure and cohort by utilizing the 11 participating CTN 0049 research teams to recruit their randomized participants into the CTN 0064 study.

CTN 0064 has two main components: Component 1 is the baseline assessment for CTN 0064. It will also serve as a long-term follow-up assessment for CTN 0049 for those who consent to participate in CTN 0064. Participants whose HCV antibody test result is positive in this baseline assessment will be invited to enroll in Component 2. Component 2 is an RCT that will assess the effectiveness of a Care Facilitation intervention (compared to Control) in moving HIV/HCV co-infected substance users forward along the HCV care continuum. The study's primary objective is based on Component 2 and will be operationalized as movement through a series of (potentially non-sequential) pre-defined, clinical steps along the HCV care continuum (including the ultimate step, sustained virologic response to treatment at 12 weeks post treatment completion [SVR12]) (AASLD/IDSA/IAS-USA). Secondary objectives will be to assess: 1) success at each step in the HCV care continuum, 2) engagement in HIV care and substance use treatment, and 3) HIV viral suppression as well as 4) to examine other long-term outcomes of the CTN 0049 cohort.

All adults who were randomized into the CTN 0049 study and who provided consent to be contacted about future studies (hereafter, referred to as the "CTN 0049 cohort") will be invited to enroll in the CTN 0064 study. All participants will provide informed consent and complete Component 1, consisting of: 1) a computer assisted personal interview or CAPI (capturing history of HIV care, HCV testing and care, substance use and substance use treatment; mental health; demographics; and socio-economic factors), 2) HCV antibody screening via rapid HCV test (and, if HCV antibody positive, HCV RNA testing via venipuncture), 3) associated pre-/post-HCV test information and counseling, 4) blood specimen collection via venipuncture, and 5) drug/alcohol toxicology screening (via urine evaluation). The blood specimens of all participants will be assessed for HIV viral load and CD4 count. The blood specimens for the subset of participants who screen as HCV antibody positive will be assessed for HCV RNA to determine if their HCV infection is active.

Participants who screen as HCV antibody positive will be randomized into Component 2 and assigned to one of two groups: 1) HCV Care Facilitation intervention or 2) Control. The Care Facilitation intervention group will receive up to 12 sessions during a 6-month intervention period. Follow-up visits with both groups will be conducted at approximately 6 and 12 months post-randomization. These visits will consist of CAPI, blood specimen collection, and drug/alcohol toxicology screening. Medical records will be reviewed to document HCV testing, receipt and use of HCV clinical evaluation, care and treatment (as applicable); and HIV care and treatment before and during the study period.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 422
• Est. completion date: May 9, 2018
• Est. primary completion date: May 9, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

By virtue of participating individuals being recruited from the CTN-0049 cohort, they will be:

1. HIV-infected and

2. 18 years of age or older

3. Be able to communicate in English

Additionally, to be eligible for Component 1 they must:

4. provide informed consent, which includes being willing to provide sufficient locator information and to be tested for anti-HCV antibodies and, if antibody positive, tested for active HCV infection

5. sign a HIPAA form / medical record release form to facilitate medical record abstraction

Finally, to continue on to Component 2, they must:

6. provide sufficient locator information

7. report living in the vicinity and being able to return for follow-up visits

8. complete the baseline assessments

9. complete the blood draw

10. test as HCV antibody positive via study Component 1 and,

11. agree to be randomized in Component 2

Exclusion Criteria:

Individuals will be excluded from participation if they:

1. have significant cognitive or developmental impairment

2. are terminated via Site Principal Investigator decision/discretion with agreement from study Lead Investigator

3. are currently in jail, prison or any inpatient overnight facility as required by court of law or have a pending legal action which may prevent an individual from completing the study

Additionally, individuals may participate in Component 1, but will be excluded from Component 2 if they:

4. are currently on HCV therapy/medications at baseline

5. have completed a course of HCV medications in the last 12 weeks based on self-report.

It should be noted that pregnancy is not an exclusion criterion. Therefore, sites may enroll pregnant women and/or follow-up with already enrolled women who become pregnant after enrollment in the study provided that they have local IRB approval to do so.

Related Conditions & MeSH terms

• AIDS
• Hepatitis
• Hepatitis C
• HIV
• Substance Use

Intervention

Other:
• Control Group
After screening HCV antibody positive, participants will receive an appointment and reminder card to return for their HCV RNA results. If HCV RNA positive, study staff will attempt to make an appointment for the participant's next step in the HCV continuum. If a participant attends the "next step" visit, the participant would be subject to whatever is the local standard of care at that clinic/agency from that point forward.

Behavioral:
• Care Facilitation Group
The same will occur for intervention participants, yet an HCV care facilitator will motivate them to return for their HCV RNA results; appointment reminders will be made prior to the "next step" visit; follow-up contact will be made for missed appointments; and the HCV care facilitator will coordinate and link the participant to available community resources (e.g., mental health, housing agencies) by scheduling appointments, arranging transportation, and helping to complete any clinic registration (or other) paperwork that agencies may require to access services.

Locations

Country	Name	City	State
United States	Grady Memorial Hospital / Ponce de Leon Center	Atlanta	Georgia
United States	Johns Hopkins Hospital / Moore Clinic	Baltimore	Maryland
United States	University Hospital at University of Alabama at Birmingham	Birmingham	Alabama
United States	Boston University Medical Center	Boston	Massachusetts
United States	John H. Stroger Jr. Hospital of Cook County	Chicago	Illinois
United States	University of Texas Southwestern	Dallas	Texas
United States	Jackson Health System Adult HIV Outpatient Clinics / University of Miami	Miami	Florida
United States	Mount Sinai - St. Luke's Roosevelt Hospital Center	New York	New York
United States	Hahnemann University Hospital	Philadelphia	Pennsylvania
United States	University of Pittsburgh Medical Center Presbyterian / Pittsburgh AIDS Center for Treatment	Pittsburgh	Pennsylvania
United States	Los Angeles BioMedical Research Institute at Harbor-UCLA Medical Center	Torrance	California

Sponsors (18)

Lead Sponsor

Collaborator

Columbia University

Boston University, Grady Memorial Hospital, Hahnemann University Hospital, Icahn School of Medicine at Mount Sinai, Jackson Health System, John H. Stroger Hospital, Johns Hopkins University, Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, National Institute on Drug Abuse (NIDA), St. Luke's-Roosevelt Hospital Center, The Emmes Company, LLC, University Hospital Birmingham, University of California, San Francisco, University of Miami, University of Pittsburgh Medical Center, University of Texas, Weill Medical College of Cornell University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Forward movement along the HCV care continuum assessed as the difference between the number of steps completed pre- and post-randomization (among Component 2 participants)	The primary outcome is a count variable: total # of completed steps along the HCV care continuum by 14 months post-randomization (this is the outside window for the 12-month follow-up visit) minus the total number of steps completed within 12 months prior to baseline. Participants' final step on the HCV care continuum will be assessed the last time they are observed in medical records within the 14-month-long follow-up period. Because the entire sample has HIV, we include 2 HIV-related steps: Receipt of HCV RNA result -- result received within 3 months of baseline; HIV primary care visit -- completion of 1 visit with an HIV primary care provider; Initiated HIV ART; HCV evaluation; HCV treatment offered and declined or prescription process initiated; HCV treatment initiated; Course of HCV treatment completed; SVR12 (sustained virologic response) achieved at 12 or more weeks after treatment completion	14 months post-randomization (this is the outside window for the 12-month follow-up visit)
Secondary	HIV viral suppression	Suppression binary defined as viral load <=200 copies/ml (yes) vs. viral load >200 copies/ml or all-cause mortality (no)	Assessed at the CTN 0064 baseline visit
Secondary	HIV care visit attendance		Assessed in the 6-month time period before the CTN 0064 baseline visit
Secondary	All-cause mortality		Time period will vary by participant between 9 months and 4 years depending when they were randomized into CTN 0049 and when they complete the CTN 0064 baseline assessment.