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
Sponsors and collaborators
William Stoops
Lead sponsor
University of Kentucky
Sponsor institution
National Institute on Drug Abuse (NIDA)
Collaborator