Cocaine Use Reduction and Health
- Conditions
- Cocaine Use Disorder
- Interventions
- Behavioral: Contingency Management
- Registration Number
- NCT03224546
- Lead Sponsor
- William Stoops
- Brief Summary
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 cocaine use. These data will be used to change current accepted cocaine treatment endpoints and accelerate identification of therapies for cocaine use disorder.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 127
- Age 18 or older
- Self-report of recent cocaine use verified by a cocaine-positive urine sample
- Meet moderate-severe Cocaine Use Disorder Criteria
- Seeking treatment for their cocaine use
- Able to commit to 12-week intervention, plus 24-week follow up
- History of serious physical or psychiatric disease (e.g., physical dependence on any drug requiring medically managed detoxification, unstable angina, uncontrolled cardiac arrhythmia, aortic stenosis, self-reported compromised immune function, extreme hypersensitivity/allergy to candida yeast or similar products, severe diagnosis for other substance use disorder) that would interfere with study participation
- Current physical or psychiatric disease that would interfere with study participation
- Poor veinous access, precluding blood draws
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Low Value Alternative Reinforcer Group Contingency Management This group will receive payment for providing cocaine negative urine samples throughout the trial. High Value Alternative Reinforcer Group Contingency Management This group will receive payment for providing cocaine negative urine samples throughout the trial.
- Primary Outcome Measures
Name Time Method Endothelin-1 Levels Week 12 of study participation Endothelin-1 levels will be measured. They will be recorded in pg/ml.
Mean Arterial Pressure Week 12 of participation Mean Arterial Pressure was recorded during subject visits and is recorded in mm Hg
- Secondary Outcome Measures
Name Time Method Interleukin-10 Week 12 of study participation Interleukin-10 levels will be measured throughout subject participation. They will be recorded in pg/ml.
Hamilton Depression Scale Score Week 12 of Participation Score on the Hamilton Depression Inventory. Higher scores indicate greater depression symptoms. Minimum = 0, Maximum =56.
Criteria for Cocaine Use Disorder Diagnosis Week 12 of Participation Number of criteria met on a Structured Clinical Interview as endorsed yes/no on a series of 11 questions on a scale. Range = 0-11. Higher scores indicate greater severity of Cocaine Use Disorder (e.g., more life problems due to cocaine use).
Total Sleep Time Week 12 of participation Sleep time the night before in minutes
Reactive Hyperemia Index Week 12 of participation Measure of peripheral arterial tonomotry which assesses peripheral microvascular function through changes in amplitude of pulses in fingertips. Reactive hyperemia index (RHI) is "determined by calculating the ratio of hyperemic pressure (RHm) to baseline pressure (BLm) in the measurement and control arms (RHc and BLc respectively)" (Rosenberry and Nelson, 2020). This yields a natural log RHI ratio with higher scores indicating worse microvascular function. This yields a natural log RHI ratio with higher scores indicating worse microvascular function. Being calculated as a natural log, there range is infinite.
Trial Locations
- Locations (1)
University of Kentucky
🇺🇸Lexington, Kentucky, United States