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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04499651
Other study ID # ISR-US-18-10586
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date July 31, 2020
Est. completion date February 22, 2021

Study information

Verified date February 2021
Source University of California, Los Angeles
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will evaluate the efficacy of navigation for hepatitis C treatment in people living with both HIV and HCV with criminal justice involvement.


Description:

Hepatitis C (HCV) is the most common chronic, blood-borne infection in the U.S. and, untreated, can result in liver failure and liver cancer. Despite advances in treatment and remarkable improvements in cure rates, very few persons with chronic HCV infection are receiving this treatment, especially among people who use drugs, who are also disproportionately HIV-infected and incarcerated. Existing efforts to ensure linkage to and retention in medical care following release from incarceration among people living with both HIV and HCV are generally insufficient. Increasing treatment engagement following release from incarceration can drastically reduce HCV and HIV in the blood, which can limit transmission to sexual and injection drug use partners. The goal of this study is to evaluate the effect of a novel navigation intervention to improve HIV/HCV treatment engagement among HIV/HCV co-infected adults with criminal justice involvement. The investigators hypothesize that the navigation intervention is more effective than the current standard-of-care approaches to link this population of adults to HIV/HCV treatment. All participants, regardless of study arm, will complete one baseline interview around the time of study enrollment. Follow-up interviews are done at 3 months and 8 months following enrollment (if enrolled in the community) or after release from jail (if enrolled in the jail). Blood samples to analyze the HCV RNA will be collected or requested from participants' clinics both for the baseline assessment and the assessment conducted 12 weeks after completion of the HCV treatment course (if the HCV RNA result cannot be obtained at 12 weeks, it will done at the 8-month follow-up interview). HIV RNA will be collected from the clinics. In addition to the interviews and the HCV/HIV RNA assessments, participants assigned to the intervention arm will engage in a six- or seven-session navigation intervention. Participants will be in the study for about 12 months but no more than 3 years.


Recruitment information / eligibility

Status Terminated
Enrollment 1
Est. completion date February 22, 2021
Est. primary completion date February 22, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria (if recruited in jail) 1. Diagnosed HIV+/HCV co-infection; 2. 18 years of age or older; 3. non-cis women; 4. Fluent in speaking English; 5. Have an anticipated sentence of no more than 12 months; 6. Have detectable Hepatitis C viral load 7. Going to live in LA County, Kern County, San Diego County, Riverside County, Ventura County or San Bernardino County If recruited outside of jail: 1. Diagnosed HIV+/HCV co-infection; 2. 18 years of age or older; 3. non-cis women; 4. Fluent in speaking English; 5. Incarceration history within the last 12 months of enrollment; 6. Have detectable Hepatitis C viral load 7. Going to live in LA County, Kern County, San Diego County, Riverside County, Ventura County or San Bernardino County Exclusion Criteria: 1. Inability to give informed consent 2. CD4 count<200

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Navigation
Trained study navigators will provide one-on-one learning sessions and accompaniments to criminal-justice involved people to help link them to HIV/Hepatitis C care

Locations

Country Name City State
United States UCLA Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Undetectable Hepatitis C RNA Undetectable Hepatitis C RNA 8 months
Primary Undetectable HIV RNA HIV RNA <40 copies/ml 8 months
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