ClinicalTrials.Veeva

Menu

SBI for PSM and PSD

C

California State University, Long Beach

Status and phase

Invitation-only
Phase 1

Conditions

Prescription Stimulant Misuse
Prescription Stimulant Diversion

Treatments

Behavioral: F2F
Behavioral: Control
Behavioral: eSBI

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06923384
1R34DA056596-01A1 (U.S. NIH Grant/Contract)
R34DA056596 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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.

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 3 patient groups, including a placebo group

Control
Placebo Comparator group
Description:
Students complete the assessments at each time point, but do not receive any intervention or informational material.
Treatment:
Behavioral: Control
F2F
Experimental group
Description:
After T1 assessment, students meet with a trained provider and receive prevention or brief intervention. Students then complete assessments at two additional times.
Treatment:
Behavioral: F2F
eSBI
Experimental group
Description:
After T1 assessment, students watch and respond to a prevention or brief intervention video series. Students then complete assessments at two additional times.
Treatment:
Behavioral: eSBI

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems