Encouraging Abstinence Behavior in a Drug Epidemic: Optimizing Dynamic Incentives

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWake Forest University Health Sciences

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age at least 18 years old;

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

Have access to a smartphone (iOS or Android) with data plan and willing to download DynamiCare app;

Have an email and can access it from their smartphone;

Disqualifiers

Have evidence of active (non-substance related) psychosis that might impair participation as determined by the PI.

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • App-Based Contingency Management

    Behavioral

    Participants will receive financial incentives for submitting randomly generated drug-negative saliva tests across the intervention period.

  • Sham Control

    Behavioral

    Participants get access to the DynamiCare app but will not be provided with financial incentives.

Treatment groups

600 Participants
are divided into 7 treatment groups

7

Treatment groups

See each treatment group below.

Group A: ControlActive comparator 1 intervention
Group B: Escalating LowExperimental treatment 1 intervention
Group C: Escalating HighExperimental treatment 1 intervention
Group D: De-Escalating LowExperimental treatment 1 intervention
Group E: De-Escalating HighExperimental treatment 1 intervention
Group F: Constant HighExperimental treatment 1 intervention
Group G: Constant LowExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percent of Negative Saliva Tests

Percent of tests negative for non-medical opioids, cocaine, or stimulant

Time frame
month 3
2

Percent of App Acceptability

Percent of eligible population which accepts app

Time frame
month 12

Secondary outcomes

1

Percent of Psychotherapy Visits Attended

Time frame
month 3
2

Percent of Treatment Discharge Against Medical Advice

Percent of patients of discharging from treatment before completion

Time frame
month 3
3

Percent of Relapse

Percent of patients who step up in care to inpatient, residential, or day partial hospitalization treatment program (PHP)

Time frame
month 3
4

Percent of transition to step-down care

Percent of patients who transition to appropriate step-down care within 14 days of enrollment in treatment

Time frame
Day 14

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Wake Forest University Health Sciences

Lead sponsor

University of Chicago

Collaborator

Rogers Behavioral Health

Collaborator

University of California Santa Cruz

Collaborator