Transforming the Cascade Of Hepatitis C Care

Sponsor
University of Pittsburgh (Other)
Overall Status
Completed
CT.gov ID
NCT03226509
Collaborator
(none)
325
1
52.4
6.2

Study Details

Study Description

Brief Summary

Several factors are barriers to effective Hepatitis C care: 1) The majority of Hepatitis C Virus (HCV)-positive patients (45-85 percent) are unaware that they are infected; 2) Only a small minority of those in need of treatment receive it; 3) Members of minorities and older patients are even less likely to receive needed care; and 4) Until recently, even those who were treated had a low chance of clearing the virus or achieving cure; 5) It is possible that older attitudes and expectation of futility might continue to persist among patients and provider in primary care settings.

Community Health Centers are often the most culturally appropriate and accessible choices, particularly for underserved populations, with the benefit of ongoing trust and relationships with patients. Therefore, these can be ideal places to deliver complex HCV care if they possess the needed expertise. However, most community-based primary care and community health centers lack access to Hepatitis C evaluation and treatment services, leading to a major public health problem.

Thus, investigators propose to implement and evaluate a pragmatic trial to implement and evaluate a multi-disciplinary model for HCV treatment at Currently, the treatment initiation rates at each of these sites is estimated as less than 10%. The investigators hypothesize that our project will increase the rate of participation in all the steps of the HCV care cascade and ultimately lead to more than doubled rates of treatment uptake

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Primary Objective:

    Determine uptake, effectiveness and safety of IFN-free, DAAs among "real world" patients, including those with multiple comorbidities, in the primary care setting.

    Secondary Objective(s):
    1. Demonstrate the transformation of the cascade of Hepatitis C Care at 3 primary care clinics in terms of changes from baseline in rates for rates of access to HCV care including HCV screening, evaluation, treatment consideration, treatment uptake, completion, loss to follow-up, and treatment success rate.

    2. Advance understanding of hepatitis C related decision-making in the era of Interferon (IFN)-free Direct acting agents (DAAs) by examining the context, needs, motivators, barriers, and preferences among patients and providers to the delivery of hepatitis C treatment at primary care clinics

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    325 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Transforming the Cascade of Hepatitis C Care
    Actual Study Start Date :
    Sep 1, 2016
    Actual Primary Completion Date :
    Sep 30, 2019
    Actual Study Completion Date :
    Jan 14, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Percentage of patients achieving sustained viral response 12 weeks post treatment (SVR 12) over a three year intervention period. [three years]

      measure percentage of patients moving through the cascade of care to cure of condition (SVR 12)

    Secondary Outcome Measures

    1. Rates of Hepatitis C Virus (HCV) screening [three years]

      Percentage of at risk patients in the practice who have a completed HCV antibody test

    2. Rate of Chronic Hepatitis C evaluation [three years]

      Percentage of patients with a positive HCV antibody test who have a HCV polymerase chain reaction (PCR) viral load completed

    3. Rate of treatment consideration [three years]

      Percentage of consented patients with a positive HCV viral load who have a clinical evaluation and assessment of psychosocial readiness for treatment documented in the medical record

    4. Rate of treatment uptake [three years]

      Percentage of patients recommended for treatment who begin medical treatment

    5. Rate of treatment completion [three years]

      Percentage of patients that began treatment who complete the recommended course of therapy

    6. Rate of patients lost to follow up [three years]

      Percent of consented patients with a positive HCV viral load who are lost to follow up

    7. Hepatitis C capacity building among family medicine physicians (provider practice and perceived confidence): [three years]

      Endpoints related to HCV capacity building among family medicine physicians: Evaluate comfort and skill among family physicians to evaluate and treat HCV infection as measured on a qualitative survey of physicians

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • All patients with detectable HCV RNA level, currently receiving care at any of these three community health centers
    Exclusion Criteria:
    • Criteria for automatic specialty referral (exclusion from treatment at community health centers) Child Turcotte Pugh Class B or C Any history of decompensated liver disease or hepatocellular carcinoma Evidence of renal disease (GFR <50) or coexisting autoimmune condition HIV of hepatitis B co-infection

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UPMC Shadyside Family Health Center Pittsburgh Pennsylvania United States 15232

    Sponsors and Collaborators

    • University of Pittsburgh

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Norman Randall Kolb, Principle Investigator; Associate Program Director UPMC Shadyside Family Medicine Residency, University of Pittsburgh
    ClinicalTrials.gov Identifier:
    NCT03226509
    Other Study ID Numbers:
    • PRO16040427
    First Posted:
    Jul 21, 2017
    Last Update Posted:
    Jan 19, 2021
    Last Verified:
    Jan 1, 2021
    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 Norman Randall Kolb, Principle Investigator; Associate Program Director UPMC Shadyside Family Medicine Residency, University of Pittsburgh
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 19, 2021