Non-Abstinence Outcomes in Methamphetamine Use Disorder

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWilliam Stoops

About this trial

Reduced drug use is a clinically meaningful target for treatment development, but few studies have evaluated the positive impacts produced by this behavioral change, preventing adoption of this endpoint in clinical trials. The proposed research will fill that critical knowledge gap by demonstrating the biopsychosocial benefits of reduced methamphetamine use. These data will be used to change current accepted methamphetamine treatment endpoints and accelerate identification of therapies for methamphetamine use disorder.

Eligibility criteria

Qualifiers

be age 18 years or older;

self-report methamphetamine use in the week prior to screening;

provide a methamphetamine-positive urine sample at screening;

meet DSM-5 criteria for moderate-severe Methamphetamine Use Disorder (MUD);

Disqualifiers

current or past medical or psychiatric illness (e.g., physical dependence on any drug other than buprenorphine requiring medically managed detoxification, unstable angina, uncontrolled cardiac arrhythmia, aortic stenosis, self-reported compromised immune function, severe diagnosis for a SUD other than MUD or treated OUD) that would interfere with study participation in the opinion of the study physicians

poor venous access precluding blood draws

Trial design

Treatments tested in this trial

  • Contingency Management

Treatment groups

300 Participants
are divided into 2 treatment groups

Sponsors and collaborators

William Stoops

Lead sponsor

University of Kentucky

Sponsor institution

National Institute on Drug Abuse (NIDA)

Collaborator