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Hepatitis C Alcohol Reduction Treatment (HepART-RCT)

Primary Purpose

Hepatitis C, Chronic; AUD

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Brief alcohol counseling
Group and Individual Therapy Sessions
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Hepatitis C, Chronic; AUD focused on measuring HCV, hepatitis C, alcohol, integrated care

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

  • Ever HCV-infected chronic HCV
  • Appropriate score on the Alcohol Use Disorder Identification Test (AUDIT)

    • Females, ≥4
    • Males, ≥8
  • Consumed alcohol in past 60 days
  • Not currently attending alcohol treatment services more than once every two weeks. If you attend treatment services at least once every two weeks, you must have either drunk alcohol heavily in the past 2 weeks or have drunk alcohol at least 7 of the past 14 days or your medical provider must have assessed that you would benefit from alcohol treatment services offered by this study

    * Patient at one of the 3 clinic sites

  • 18 or older
  • English-speaking
  • OK to have HIV, substance use or other co-morbidities, or receiving HCV antiviral treatment

Exclusion criteria

  • Psychotic
  • Insurmountable transportation barriers (can receive individual therapy by phone but need appointments with HCV provider at 3 and 6 months and ideally some in-person group therapy)

Sites / Locations

  • Duke University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Medical provider (MP) brief alcohol counseling & referral

Brief alcohol counseling & 6 months of HCV-alcohol treatment

Arm Description

Screening of HCV-infected patients for alcohol use using the 10-item Alcohol Use Disorders Identification Test (AUDIT). Patients self-administer the AUDIT. HCV providers review the AUDIT with the patient. If the patient is using any alcohol, the HCV provider conducts brief alcohol counseling using the FRAMES model, based on the evidence-based Screening, Brief Intervention, and Referral to Treatment (SBIRT) method. Medical provider will explain the importance of alcohol abstinence in the presence of HCV infection. Patient is referred to an alcohol treatment programs outside the liver clinic. Typical counseling will take the form of individual and group therapy.

Steps 1 through 5 as described in comparator arm above. 6 months of group therapy, offered weekly. 6 months of individual therapy, in person or by phone, offered every two weeks. Therapy content emphasizes interplay between alcohol use and liver health/HCV. Informal collaboration between HCV providers and addictions therapists. Shared EMR charting. Referral to study-provided psychiatry as needed.

Outcomes

Primary Outcome Measures

Alcohol abstinence rates at 6 months after consent
Investigators will compare the two treatment arms on occurrence and amount of past 180 days of drinking using the timeline follow-back method, allowing the investigators to assess change in number of drinking days, periods of abstinence, and total grams of alcohol consumed.

Secondary Outcome Measures

Relapse rate at 12 months after consent
Investigators will compare the two treatment arms on periods of abstinence and number of drinking days using the timeline follow-back method for the 180 days between 6 and 12 months since study consent.
Other alcohol use indicators
At 3, 6 and 12 months, investigators will assess the number of heavy drinking days and grams of alcohol consumed and compare between the two treatment arms.
Illicit drug use
At 3, 6 and 12 months, investigators will assess illicit drug use based on positive/negative urine toxicology screens and compare between the two treatment arms.

Full Information

First Posted
June 26, 2014
Last Updated
October 17, 2018
Sponsor
Duke University
Collaborators
University of North Carolina, Chapel Hill, Durham VA Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02176980
Brief Title
Hepatitis C Alcohol Reduction Treatment
Acronym
HepART-RCT
Official Title
Hepatitis C Alcohol Reduction Treatment - Randomized Controlled Trial (Hep ART-RCT)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
September 30, 2018 (Actual)
Study Completion Date
September 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
University of North Carolina, Chapel Hill, Durham VA Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Subjects are being asked to take part in a research study to test two levels of alcohol services for patients with hepatitis C virus (HCV) who drink alcohol. The two levels differ in intensity of alcohol services and in whether or not they include a focus on liver health. The study will look at which level of alcohol services best decreases alcohol use among patients with HCV.
Detailed Description
For people infected with hepatitis C virus (HCV), alcohol use increases the risk of hepatocellular carcinoma and progressive liver fibrosis, which can lead to cirrhosis and liver-related mortality. Integrated models of care that incorporate treatment for alcohol use, substance use, and mental health comorbidities have been called for, but few empirically tested models exist. In an R21 study, we developed and manualized an integrated behavioral-medical treatment model for patients with HCV who consume alcohol. Investigators successfully implemented a standardized alcohol screening in a liver clinic using the Alcohol Use Disorders Identification Test (AUDIT) instrument; recruited 60 patients; retained participants in group and individual therapy; integrated care between an addictions therapist and medical providers; and achieved an 85% six-month interview response rate. The alcohol abstinence rate improved from 0% at baseline to 44% at 6 months. Mean Addiction Severity Index scores were reduced by 50% for alcohol from .24 to .12, and decreased for drug use from .05 to .03. The percentage of heavy drinkers decreased from 47% to 24% (Proeschold-Bell et al., 2011). This study will conduct a randomized controlled trial that compares medical provider-delivered brief alcohol counseling plus our on-site six-month integrated treatment to brief alcohol counseling plus outside alcohol treatment referral in 279 HCV-infected patients with qualifying AUDIT alcohol scores at baseline. Participants in both arms will be treated at the Duke and UNC Liver Clinics and the Durham Veterans Affairs Medical Center. Outcome variables will be assessed at baseline, 3, 6, and 12 months. The aims are to 1) evaluate alcohol abstinence; 2) determine differences in secondary outcomes between study arms; and 3) conduct a cost effectiveness analysis. Investigators hypothesize that the intervention will significantly improve alcohol abstinence rates and significantly decrease relapse rates compared to the comparison. Investigators further hypothesize that intervention participants will report fewer drinks per week than comparison participants, have fewer positive drug screens than comparison participants, and meet the $50,000 per quality-adjusted life year gained standard established in the health economics literature.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C, Chronic; AUD
Keywords
HCV, hepatitis C, alcohol, integrated care

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
182 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Medical provider (MP) brief alcohol counseling & referral
Arm Type
Active Comparator
Arm Description
Screening of HCV-infected patients for alcohol use using the 10-item Alcohol Use Disorders Identification Test (AUDIT). Patients self-administer the AUDIT. HCV providers review the AUDIT with the patient. If the patient is using any alcohol, the HCV provider conducts brief alcohol counseling using the FRAMES model, based on the evidence-based Screening, Brief Intervention, and Referral to Treatment (SBIRT) method. Medical provider will explain the importance of alcohol abstinence in the presence of HCV infection. Patient is referred to an alcohol treatment programs outside the liver clinic. Typical counseling will take the form of individual and group therapy.
Arm Title
Brief alcohol counseling & 6 months of HCV-alcohol treatment
Arm Type
Experimental
Arm Description
Steps 1 through 5 as described in comparator arm above. 6 months of group therapy, offered weekly. 6 months of individual therapy, in person or by phone, offered every two weeks. Therapy content emphasizes interplay between alcohol use and liver health/HCV. Informal collaboration between HCV providers and addictions therapists. Shared EMR charting. Referral to study-provided psychiatry as needed.
Intervention Type
Behavioral
Intervention Name(s)
Brief alcohol counseling
Intervention Description
Medical provider gives feedback on how the patient's alcohol use may affect their current and future health, noting that it is the patient's responsibility to change behavior; giving advice to stop drinking based on medical concern; giving a menu of options for cutting down on drinking; expressing empathy; and reinforcing the patient's self-efficacy to change.
Intervention Type
Behavioral
Intervention Name(s)
Group and Individual Therapy Sessions
Intervention Description
Session content integrates HCV and alcohol issues in treatment, liver health, and personal realms. Sessions include psychoeducational content on how alcohol affects the liver among people with HCV; HCV stigma; family issues around drinking and the HCV diagnosis; nutrition; life goals and positive affect; and alcohol reduction strategies.
Primary Outcome Measure Information:
Title
Alcohol abstinence rates at 6 months after consent
Description
Investigators will compare the two treatment arms on occurrence and amount of past 180 days of drinking using the timeline follow-back method, allowing the investigators to assess change in number of drinking days, periods of abstinence, and total grams of alcohol consumed.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Relapse rate at 12 months after consent
Description
Investigators will compare the two treatment arms on periods of abstinence and number of drinking days using the timeline follow-back method for the 180 days between 6 and 12 months since study consent.
Time Frame
12 months
Title
Other alcohol use indicators
Description
At 3, 6 and 12 months, investigators will assess the number of heavy drinking days and grams of alcohol consumed and compare between the two treatment arms.
Time Frame
3, 6 and 12 months
Title
Illicit drug use
Description
At 3, 6 and 12 months, investigators will assess illicit drug use based on positive/negative urine toxicology screens and compare between the two treatment arms.
Time Frame
3, 6 and 12 months
Other Pre-specified Outcome Measures:
Title
Cost effectiveness analysis of the intervention versus brief alcohol counseling and referral out
Description
The incremental cost-effectiveness ratio (ICER) will be absolute difference in costs divided by the absolute difference in various effectiveness measures between the 2 interventions.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Ever HCV-infected chronic HCV Appropriate score on the Alcohol Use Disorder Identification Test (AUDIT) Females, ≥4 Males, ≥8 Consumed alcohol in past 60 days Not currently attending alcohol treatment services more than once every two weeks. If you attend treatment services at least once every two weeks, you must have either drunk alcohol heavily in the past 2 weeks or have drunk alcohol at least 7 of the past 14 days or your medical provider must have assessed that you would benefit from alcohol treatment services offered by this study * Patient at one of the 3 clinic sites 18 or older English-speaking OK to have HIV, substance use or other co-morbidities, or receiving HCV antiviral treatment Exclusion criteria Psychotic Insurmountable transportation barriers (can receive individual therapy by phone but need appointments with HCV provider at 3 and 6 months and ideally some in-person group therapy)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew Muir, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22134784
Citation
Proeschold-Bell RJ, Patkar AA, Naggie S, Coward L, Mannelli P, Yao J, Bixby P, Muir AJ. An integrated alcohol abuse and medical treatment model for patients with hepatitis C. Dig Dis Sci. 2012 Apr;57(4):1083-91. doi: 10.1007/s10620-011-1976-4. Epub 2011 Dec 2.
Results Reference
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PubMed Identifier
30006024
Citation
Proeschold-Bell RJ, Evon DM, Makarushka C, Wong JB, Datta SK, Yao J, Patkar AA, Mannelli P, Hodge T, Naggie S, Wilder JM, Fried MW, Niedzwiecki D, Muir AJ. The Hepatitis C-Alcohol Reduction Treatment (Hep ART) intervention: Study protocol of a multi-center randomized controlled trial. Contemp Clin Trials. 2018 Sep;72:73-85. doi: 10.1016/j.cct.2018.07.003. Epub 2018 Jul 10.
Results Reference
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Hepatitis C Alcohol Reduction Treatment

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