SBI for PSM and PSD
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: F2F, eSBI, Control.
- Who it may be relevant to
- Registry conditions: Prescription Stimulant Misuse, Prescription Stimulant Diversion. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Screening and Brief Intervention for Prescription Stimulant Misuse and Diversion: Refining and Piloting a Curriculum for College Health Providers
Overview
A pilot randomized controlled trial to assess the feasibility, acceptability, and impact of screening and brief intervention to address prescription stimulant misuse and diversion among college students.
Detailed description
A screening and brief intervention including a control group, face-to-face group, and e-intervention group where the focus is prevention or brief intervention or referral to treatment related to students prescription stimulant misuse and diversion behaviors. Students will complete assessments at three time points, and the health providers who implement the intervention will also complete assessments.
Interventions
- Behavioral F2F
After T1 assessment, students meet with a trained provider and receive prevention or brief intervention. Students then complete assessments at two additional times. - Behavioral eSBI
After T1 assessment, students watch and respond to a prevention or brief intervention video series. Students then complete assessments at two additional times. - Behavioral Control
Students complete the assessments at each time point, but do not receive any intervention or informational material.
Primary outcome measures
- Prescription Stimulant Misuse [Time frame: 30 days]
- Prescription Stimulant Diversion [Time frame: 30 days]
Secondary outcome measures (2)
- PSM Intentions [Time frame: 30 days]
- PSD Intentions [Time frame: 30 days]
Eligibility criteria
Inclusion criteria
Age 18 and student at the campus serving as the intervention site; Passive recruitment: Student has a scheduled appointment for a physical/wellness exam. Active recruitment: Student has a past 3 month history of PSM or PSD.
Exclusion criteria
Any eligible student who, during the course of the session, demonstrates the need for immediate mental health services, will have the study session terminated so that participant can receive needed care.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Other
Study locations
United States · 1 center
- CSULB — Long Beach
Identifiers
NCT: NCT06923384 · R34DA056596 · 1R34DA056596-01A1