SBI for PSM and PSD

Phase 1Enrolling By InvitationNCT06923384

California State University, Long Beach120 enrolled

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.

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

120

Conditions

Prescription Stimulant Misuse Prescription Stimulant Diversion

Interventions

F2FBEHAVIORAL

After T1 assessment, students meet with a trained provider and receive prevention or brief intervention. Students then complete assessments at two additional times.

eSBIBEHAVIORAL

After T1 assessment, students watch and respond to a prevention or brief intervention video series. Students then complete assessments at two additional times.

ControlBEHAVIORAL

Students complete the assessments at each time point, but do not receive any intervention or informational material.

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

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.

Locations (1)

CSULB

Long Beach, California, United States

Outcomes

Primary Outcomes

Prescription Stimulant Misuse

Students report on their experience with prescription stimulant misuse behaviors. PSM is assessed at T1, pre-intervention, and T3, 30-Days post intervention.

Time frame: 30 days

Prescription Stimulant Diversion

Students report on their experience with prescription stimulant diversion behaviors. PSD is assessed at T1, pre-intervention, and T3, 30-Days post intervention.

Time frame: 30 days

Secondary Outcomes

PSM Intentions

Intention to engage in PSM is measured at T1 (pre-intervention), T2 (immediate post), and T3 (30 Day post intervention)

Time frame: 30 days

PSD Intentions

Intention to engage in PSM is measured at T1 (pre-intervention), T2 (immediate post), and T3 (30 Day post intervention).

Time frame: 30 days

Data from ClinicalTrials.gov

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