RECRUITING

Encouraging Abstinence Behavior in a Drug Epidemic

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

Combatting the rise of the opioid epidemic is a central challenge of U.S. health care policy. A promising approach for improving welfare and decreasing medical costs of people with substance abuse disorders is offering incentive payments for healthy behaviors. This approach, broadly known as "contingency management" in the medical literature, has repeatedly shown to be effective in treating substance abuse. However, the use of incentives by treatment facilities remains extremely low. Furthermore, it is not well understood how to design optimal incentives to treat opioid abuse. This project will conduct a randomized evaluation of two types of dynamically adjusting incentive schedules for people with opioid use disorders or cocaine use disorders: "escalating" schedules where incentive amounts increase with success to increase incentive power, and "de-escalating" schedules where incentive amounts decrease with success to improve incentive targeting. Both schemes are implemented with a novel "turnkey" mobile application, making them uniquely low-cost, low-hassle, and scalable. Effects will be measured on abstinence outcomes, including longest duration of abstinence and the percentage of negative drug tests. In combination with survey data, variation from the experiment will shed light on the barriers to abstinence more broadly and inform the understanding of optimal incentive design.

Official Title

Encouraging Abstinence Behavior in a Drug Epidemic

Quick Facts

Study Start:2021-09-15
Study Completion:2024-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04927143

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. 1. Age at least 18 years old;
  2. 2. Meet DSM-5 OUD, CoUD, or MUD criteria as evidenced by an OUD CPT code F11\* (opioid related disorders), a CoUD CPT code F14\* (cocaine related disorders), a MUD CPT code F15.1/F15.2 or other clinical notes indicating illicit opioid/cocaine/methamphetamine use for treatment;
  3. 3. Have access to a smartphone (iOS or Android) with data plan and willing to download DynamiCare app;
  4. 4. Have an email and can access it from their smartphone;
  5. 5. Are in residential, day (PHP), partial day (IOP), or outpatient (OP) AODA treatment;
  6. 6. Are likely to be helped by contingency management because at least ONE of the following conditions is true:
  7. 1. Were first enrolled in residential, PHP, or IOP substance use treatment no longer than 2 treatment weeks (14 days/encounters of treatment) prior to providing informed consent.
  8. 2. Used non-medical opioids, cocaine, and/or methamphetamine within the last 21 days.
  9. 7. Understands English.
  1. 1. Have evidence of active (non-substance related) psychosis that might impair participation as determined by the PI.
  2. 2. Has significant cognitive impairment that might confound participation as determined by the PI or are so significantly cognitively impaired that they have a legal guardian.

Contacts and Locations

Study Contact

Gary Dennison
CONTACT
414-385-1913
gary.dennison@aah.org
Bianca Burrell, BS
CONTACT
bianca.burrell@aah.org

Principal Investigator

Michael Fendrich, PhD
PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences

Study Locations (Sites)

Rogers Behavioral Health
Oconomowoc, Wisconsin, 53066
United States
Advocate Aurora Behavioral Health Services
Wauwatosa, Wisconsin, 53212
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

  • Michael Fendrich, PhD, PRINCIPAL_INVESTIGATOR, Wake Forest University Health Sciences

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 Date2021-09-15
Study Completion Date2024-12

Study Record Updates

Study Start Date2021-09-15
Study Completion Date2024-12

Terms related to this study

Keywords Provided by Researchers

  • contingency management
  • app-based treatment

Additional Relevant MeSH Terms

  • Opioid-use Disorder
  • Cocaine Use Disorder
  • Opioid Use
  • Cocaine Use
  • Substance Use
  • Methamphetamine Abuse
  • Methamphetamine-dependence