ACTIVE_NOT_RECRUITING

Dual Reinforcement Contingency Management for Alcohol Use Disorders

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

Phosphatidylethanol (PEth) is a direct biomarker of alcohol that can detect moderate to heavy drinking with high sensitivity and specificity over 3-week periods. Reinforcing negative PEth results alongside attendance may increase the proportion of participants who respond to CM during and post treatment. In the proposed study, the investigators will collect PEth samples every 3 weeks for 12 weeks in 150 participants initiating outpatient treatment for alcohol use disorders. Using a two-group randomized design, participants will be assigned to standard care with PEth monitoring alone or with CM for attending treatment and submitting PEth negative samples. Compared to standard care and monitoring, the investigators expect that the CM intervention will result in greater attendance, more PEth negative samples, and higher proportions of self-reported non-drinking days, along with lower proportions of heavy drinking days, over the short term and the long term, measured throughout a 12-month follow-up. The investigators anticipate that the reinforcement intervention may decrease other drug use and sexual risk behaviors that spread HIV, reduce psychiatric symptoms, and improve quality of life as well.

Official Title

Dual Reinforcement Contingency Management for Alcohol Use Disorders

Quick Facts

Study Start:2020-01-22
Study Completion:2025-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT04064463

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * in intensive outpatient treatment
  2. * DSM-5 diagnosis of an alcohol use disorder
  1. * have a condition that may hinder study participation

Contacts and Locations

Principal Investigator

Sheila Alessi, Ph.D.
PRINCIPAL_INVESTIGATOR
UConn Health

Study Locations (Sites)

The Village
Hartford, Connecticut, 06105
United States

Collaborators and Investigators

Sponsor: UConn Health

  • Sheila Alessi, Ph.D., PRINCIPAL_INVESTIGATOR, UConn Health

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 Date2020-01-22
Study Completion Date2025-09

Study Record Updates

Study Start Date2020-01-22
Study Completion Date2025-09

Terms related to this study

Additional Relevant MeSH Terms

  • Alcohol Use Disorder
  • Contingency Management