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Counseling Hepatitis C Virus (HCV) Positive Patients for Cardiovascular Disease Risk Factors

Primary Purpose

Hepatitis C, Atherosclerosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Patient counseling for HCV associated CVD risk factors
Sponsored by
Tulane University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis C

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • HCV antibody positive tested at one of six locations in New Orleans: Ozanam Inn, New Orleans Mission, Bethel Colony South, Grace House, St. Anna's Mobile Clinic, and Ruth Fertel

Exclusion Criteria:

  • vulnerable populations including children, prisoners, pregnant women
  • non-English speaking patients since effective counseling cannot be provided

Sites / Locations

  • Tulane University HCV Testing Clinics

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

CVD risk factor counseling

Standard of care counseling

Arm Description

This arm will receive intervention 'Patient counseling for HCV associated CVD risk factors' in addition to standard of care Hepatitis C counseling. Cardiovascular risk factor counseling will include: Increased risk for atherosclerosis with chronic HCV infection Increased risk of heart attack and stroke Treatment of HCV infection and reduction of viral load reducing risk of stroke and heart attack

This arm will receive standard of care Hepatitis C counseling: HCV infection poses an increased risk for hepatocellular carcinoma Hepatitis C is a curable disease Hepatitis C is transmitted through blood to blood contact, primarily through sharing needles HCV+ individuals should be vaccinated for Hepatitis A (HAV) and Hepatitis B (HBV) HCV+ individuals should reduce alcohol intake and shellfish consumption

Outcomes

Primary Outcome Measures

Linkage to HCV Care
The percentage of patients attending their subsequent University Medical Center hepatology appointment for the treatment and control groups will be measured, indicating the effectiveness of the "augmented education package" at improving patients' willingness to treat their HCV infection.

Secondary Outcome Measures

Linkage to Primary Care
Patients referred to the primary care provider (PCP) will be tracked to assess the proportion that attended their PCP appointment, measuring the impact of the "augmented education package" at positively influencing HCV+ patients to follow up with primary care for their atherosclerotic comorbidities.

Full Information

First Posted
January 10, 2018
Last Updated
September 19, 2022
Sponsor
Tulane University
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1. Study Identification

Unique Protocol Identification Number
NCT03402334
Brief Title
Counseling Hepatitis C Virus (HCV) Positive Patients for Cardiovascular Disease Risk Factors
Official Title
Assessing Healthcare Outcomes of Hepatitis C Virus (HCV) Positive Patients Counseled for Cardiovascular Disease Risk Factors
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
March 11, 2019 (Actual)
Primary Completion Date
February 15, 2021 (Actual)
Study Completion Date
April 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tulane University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study aims to compare the effect of a cardiovascular education package intervention on treatment-seeking behavioral outcomes of HCV+ patients. This prospective multicenter trial will compare outcomes between the intervention group (HCV+ patients receiving the enhanced education package) and the control group (HCV+ patients receiving the standard of care, the basic education package). The primary outcome measured will be successful linkage to hepatology for a discussion of HCV treatment options. The secondary outcome measured will be linkage to primary care for chronic disease management.
Detailed Description
Cardiovascular diseases (CVD), including atherosclerosis, are now the leading causes of mortality both in the United States and globally. Unfortunately, the major risk factors that have been targeted by public health programs are all behavioral, and have not met with enough success. Hence, there is an acute need for more tangible interventions that afford new options to reduce disease burden from atherosclerosis. While the association of Hepatitis C virus (HCV) infection with life threatening complications such as liver cirrhosis and hepatocellular carcinoma (HCC) is well established, the recent discovery of HCV as a risk factor for atherosclerosis presents a new target for CVD control. In the largest epidemiological study of HCV and cardiovascular disease to date, HCV positive individuals were determined to have a significantly higher incidence of myocardial infarction, congestive heart failure, and corrective procedures for coronary artery disease including bypass grafting and angioplasty (1). Subsequent meta- analyses have lent increasing support to this relationship, showing adjusted odds ratios (OR) of 1.76 - 2.24 of carotid atherosclerosis in HCV+ patients (2,3). The epidemiological evidence supporting the link of HCV and atherosclerosis has been further supported by bench research elucidating the role of HCV in vascular cytotoxicity and systemic inflammation. HCV viral replication has been shown within carotid artery plaques (4), as a result of viral endocytosis through the LDL receptor (5). HCV promotes intracellular oxidative stress, monocyte recruitment, and subsequent endothelial dysfunction leading to the promotion of atherosclerosis (6). In addition, HCV infection leads to a systemic inflammatory state promoting the acceleration of arterial vascular disease (7,8). Robust evidence now supports HCV as strongly pro-atherogenic (2,9), a relationship that is irrespective of HCV genotype or degree of histological liver pathology (10). Viral RNA load of Hepatitis C has been shown to directly correlate with the atherosclerotic burden (10,11). HCV RNA levels are associated with advanced phase carotid plaques and carotid intima-media thickness (10). In addition, HCV RNA has been found in direct association with serum fibrinogen and C-reactive protein levels, which in turn were independently associated with carotid atherosclerosis (10). Together, such data suggest that managing HCV viral load will, in turn, control the cardiovascular manifestations of this disease. Similar to atherosclerotic burden, higher viral loads correlate well with increased risk of cardiovascular and cerebrovascular associated mortality (2,9,11). Recent meta-analyses show the HCV+ population with an adjusted OR of 1.3 to 1.97 for cerebrovascular incidents (12) and an adjusted OR of 1.65 for death due to cardiovascular disease (3). Of importance, combination ribavirin and interferon therapy has been shown to decrease such non-hepatic mortality as well as incidence of stroke in HCV+ patients (13,14). Thus, prompt and effective management of HCV can lead to suppression of viral loads, which can result in decreased mortality secondary to cardiovascular events (9,10). Current estimates indicate that 3.2 million people living in the United States are HCV-infected, a disease that has now surpassed HIV in annual mortality (15,16). The development of combination sofosbuvir and ledipasvir (Harvoni), a direct acting, non-interferon based therapy, has made HCV a newly curable disease. This is an exciting new field with potential for a novel anti-viral intervention to reduce the burden of atherosclerosis and the associated deaths from ischemic heart disease and strokes. Goal: To investigate the role of HCV treatment in decreasing atherosclerotic co-morbidities. Specific Aim 1 For HCV: To increase HCV healthcare-seeking behavior of HCV+ patients by educating them about their increased risk for atherosclerosis, cardiovascular disease, and cerebrovascular events. Specific Aim 2 For Atherosclerosis: To positively influence HCV+ patients to follow up with a primary care physician for either prevention or management of any potential atherosclerotic comorbidities. Methodology Tulane Medical students trained by the New Orleans Office of Public Health (OPH) currently provide HCV screening and counseling across six New Orleans community health clinics: Ozanam Inn, New Orleans Mission, Bethel Colony South, Grace House, St. Anna's Mobile Clinic, and Ruth Fertel. HCV+ patients are linked to a primary care physician (PCP) at Healthcare for the Homeless (HCH), and in addition, curative HCV treatment at University Medical Center (UMC) Hepatology Clinic. Since its inception in 2015, 936 patients have been tested through this rapidly growing community program. A randomized controlled trial will be conducted. The control will receive the current standard of care in those clinics, including the "basic education package" on HCV-associated cirrhosis and HCC. The intervention group will receive an "augmented education package" that includes all the components of the basic package, plus education on atherosclerosis and associated cardiovascular risk. All HCV + patients will be referred to a single PCP for screening, prevention, or management of atherosclerosis. Statistical data analysis will be done using Statistical Analysis Software. For Study Aim 1 Outcome Measures for HCV: The percentage of patients attending their subsequent UMC hepatology appointment for the treatment and control groups will be measured, indicating the effectiveness of the "augmented education package" at improving patients' willingness to treat their HCV infection. For Study Aim 2 Outcome Measures for Atherosclerosis: Patients referred to the PCP will be tracked to assess the proportion that attended their PCP appointment, measuring the impact of the "augmented education package" at positively influencing HCV+ patients to follow up with primary care for their atherosclerotic comorbidities.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C, Atherosclerosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a two-arm study. Group A will receive the intervention in addition to standard of care counseling while Group B will receive only standard of care counseling.
Masking
Participant
Masking Description
Single-blinded study. Participants are blinded to their designation in the study arms. Investigators cannot be blinded since the intervention they are providing is patient counseling.
Allocation
Randomized
Enrollment
231 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CVD risk factor counseling
Arm Type
Experimental
Arm Description
This arm will receive intervention 'Patient counseling for HCV associated CVD risk factors' in addition to standard of care Hepatitis C counseling. Cardiovascular risk factor counseling will include: Increased risk for atherosclerosis with chronic HCV infection Increased risk of heart attack and stroke Treatment of HCV infection and reduction of viral load reducing risk of stroke and heart attack
Arm Title
Standard of care counseling
Arm Type
No Intervention
Arm Description
This arm will receive standard of care Hepatitis C counseling: HCV infection poses an increased risk for hepatocellular carcinoma Hepatitis C is a curable disease Hepatitis C is transmitted through blood to blood contact, primarily through sharing needles HCV+ individuals should be vaccinated for Hepatitis A (HAV) and Hepatitis B (HBV) HCV+ individuals should reduce alcohol intake and shellfish consumption
Intervention Type
Behavioral
Intervention Name(s)
Patient counseling for HCV associated CVD risk factors
Intervention Description
Patients will be counseled for cardiovascular disease risk factors associated with Hepatitis C infection. Such risk factors include atherosclerosis, heart attack, and stroke. Cardiovascular risk factors can be managed through connection with primary care and reduced through curative HCV treatment.
Primary Outcome Measure Information:
Title
Linkage to HCV Care
Description
The percentage of patients attending their subsequent University Medical Center hepatology appointment for the treatment and control groups will be measured, indicating the effectiveness of the "augmented education package" at improving patients' willingness to treat their HCV infection.
Time Frame
Patient will be assessed for follow up within 6 months post counseling
Secondary Outcome Measure Information:
Title
Linkage to Primary Care
Description
Patients referred to the primary care provider (PCP) will be tracked to assess the proportion that attended their PCP appointment, measuring the impact of the "augmented education package" at positively influencing HCV+ patients to follow up with primary care for their atherosclerotic comorbidities.
Time Frame
Patient will be assessed for follow up within 6 months post counseling

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: HCV antibody positive tested at one of six locations in New Orleans: Ozanam Inn, New Orleans Mission, Bethel Colony South, Grace House, St. Anna's Mobile Clinic, and Ruth Fertel Exclusion Criteria: vulnerable populations including children, prisoners, pregnant women non-English speaking patients since effective counseling cannot be provided
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Austin T Jones, MD, PhD
Organizational Affiliation
Tulane University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tulane University HCV Testing Clinics
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data will not be disclosed
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Counseling Hepatitis C Virus (HCV) Positive Patients for Cardiovascular Disease Risk Factors

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