RECRUITING

CM for Patients With ALD After Liver Transplant

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Alcohol associated liver disease (ALD) refers to liver injury, such as cirrhosis, that is caused by alcohol use. It affects 2 million adults in the U.S. and is now the leading cause of cirrhosis-related hospitalizations, cirrhosis- related deaths, and liver transplantation. Alcohol use disorder (AUD), the root cause of ALD, affects 15 million Americans each year. While research studies have shown that behavioral therapy and medications specific for alcohol use have helped people overcome their alcohol use disorder, there has not been enough information related to how successful these treatments are specifically for people with ALD. This study will look at a behavioral treatment called "contingency management" (CM) that has shown to be effective with people with other substance use disorders. CM is based on the principles of operant conditioning that involves offering prize-based or monetary incentives to patients with substance use disorders to reduce substance use. This study will look at the efficacy and acceptability of CM in patients who received a liver transplant and have evidence of recurrent alcohol use. The proposed study is a pilot randomized controlled trial of 30 patients with ALD who received a liver transplant; 15 will be randomized to receive a 10-week CM intervention while 15 will receive treatment as usual (TAU or control). Subjects will be asked to complete 12 study visits (including Screening and Baseline Visits) that will last 1 to 2 hours each depending on the visit. All visits will be completed via Zoom or by phone. Study staff will instruct participants on how to use Zoom, if necessary. During the Screening and Baseline Visits, subjects will be: 1) asked to provide a urine test and blood draw, 2) complete the SCID-5 AUD, a semi-structured interview guide for making the major DSM-5 diagnoses, 3) complete the Iowa Gambling Test which looks at decision-making skills, 4) complete a survey that looks at the subject's quality of life after liver transplant, 4) review how much alcohol the subject has consumed in the last 30 days, 5) and if the subject has received any current AUD treatments. Once the Screening and Baseline visits are completed, subjects will be randomized to either the CM group or the TAU group. During the weekly visits, subjects will be asked to provide blood and urine samples and will be asked if they have had any alcohol since their last visit. All subjects will receive $20 for completing the visits. For those in the CM group, subjects will also receive a CM reward for negative urine and/or blood tests, depending on which results we receive first-with rewards ranging from $5 to $80 depending on the week. Additionally, during weeks 1, 5, and 10, those in the CM group will also complete the Client Satisfaction Questionnaire-8 to assess client satisfaction with CM and complete a semi-structured interview about the CM protocol as well as CM acceptability and feasibility.

Official Title

Contingency Management for Patients With Alcohol-Associated Liver Disease Following Liver Transplantation

Quick Facts

Study Start:2024-09-17
Study Completion:2026-09-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06304467

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Subjects 18 years of age or older
  2. * Have received a liver transplant
  3. * Has documented return to drinking (subjective or objective) within the past 60 days
  4. * Willing to partake in behavioral treatment for AUD
  5. * Written informed consent and ability for subject to comply with the requirements of the study.
  1. * Current treatment for another substance use disorder
  2. * Unwilling to partake in behavioral treatment for AUD
  3. * Unwilling to provide written informed consent
  4. * Non-English speaking

Contacts and Locations

Study Contact

Vanessa Ryan, MS
CONTACT
(323) 833-4676
mdryan@mednet.ucla.edu
Arpan Patel, MD
CONTACT
arpan.patel@mednet.ucla.edu

Principal Investigator

Arpan G Patel, MD
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles

Study Locations (Sites)

Pfleger Liver Institute
Los Angeles, California, 90095-1406
United States

Collaborators and Investigators

Sponsor: Arpan A. Patel, MD

  • Arpan G Patel, MD, PRINCIPAL_INVESTIGATOR, University of California, Los Angeles

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-09-17
Study Completion Date2026-09-01

Study Record Updates

Study Start Date2024-09-17
Study Completion Date2026-09-01

Terms related to this study

Keywords Provided by Researchers

  • Alcohol Liver Disease
  • Contingency Management
  • Post Liver Transplant
  • Alcohol Use Disorder
  • Post Liver Transplant Drinking

Additional Relevant MeSH Terms

  • Alcohol Use Disorder
  • Alcohol; Liver
  • Post Liver Transplant
  • Contingency Management
  • Alcohol Liver Disease