Evaluation of a Brief Computerized and Smart Phone-based Intervention for Stress in Regular Cannabis Users (DISC)
Cannabis Use Disorder
About this trial
This is an interventional treatment trial for Cannabis Use Disorder
Eligibility Criteria
Inclusion Criteria: Cannabis is the primary substance of abuse. Clinical-level Distress intolerance Index score. Current Cannabis Use Disorder diagnosis. Near-daily to daily cannabis use in past-month and past 3 months. Positive urine screen for THC Detectable skin conductance level Owns a smart phone Primary delta-9 THC user Exclusion Criteria: Presence of acute/major psychiatric disturbance Current pregnancy Change in psychotropic medication within the past month Concurrently receiving cognitive-behavioral therapy for cannabis use or emotional disorders Planning to immediately quit using cannabis EEG contraindications Kidney disease
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Emotional Engagement Distress Tolerance Intervention
Health Education Intervention
The experimental intervention (single 2.5 hour session) is comprised of video-delivered psychoeducation, adaptive skill practice, and emotional exposure. During exposure, a sequence of percussive sounds accompanied by a visual depiction of the participant's skin conductance level during exposure will be presented at the moment the participant's skin conductance returns to the relaxation baseline value. These images/sound will be intermittently sent to the participant's smart phone during the smart phone portion of the intervention.
The health education control intervention is a single 2.5 hour computerized session. It is comprised of audio-narrated videos on healthy habits and self-care in the domains of sleep, nutrition, hygiene, and physical exercise. The same sequence of percussive sounds used in the Emotional Engagement Distress Tolerance Intervention is presented alongside summary slides presenting key points on healthy habits and self-care. These images/sound will be intermittently sent to the participant's smart phone during the smart phone portion of the intervention.