Recovery Opportunities Through Ongoing Treatment Sustainment

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age13-18
SponsorUniversity of Maryland, College Park

About this trial

Adolescents in rural communities face limited access to effective substance use services, increasing their risk for opioid and other substance use disorders. This project will use an adaptive, iterative implementation approach to improve the integration of external substance use service providers into rural school settings. Findings will inform strategies to integrate and scale adolescent substance use services in schools. Support for this trial is provided by the HEAL Initiative (https://heal.nih.gov/).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Are enrolled in one of the participating schools

Are referred or independently access YSU services;

Are above age of 13

Disqualifiers

Demonstrating active, unstable or untreated psychiatric symptoms, including mania and/or psychosis that would interfere with study participation

Inability to understand the study and provide informed consent in English

Trial design

Design model

Single group

Treatments tested in this trial

  • Youth Substance Use Unit

    Behavioral

    The YSU provides adolescents access to several evidence-based interventions, including access to an on-site substance use counselor trained in evidence-based practices for adolescent SUD, peer recovery specialists, and, if indicated, virtual access to an OUD treatment provider and/or clinical psychologist for more acute and co-occurring disorder treatment.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Youth Substance Use UnitExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Reach and Engagement

Reach and Engagement will be tracked through service logs, including the number of students referred, completed referrals, and retention in care.

Time frame
From enrollment to 90-day follow-up
2

90-day Substance Use Self Report

The timeline followback will be used to assess self-reported substance use frequency

Time frame
Measured from baseline to 90-day follow-up
3

90-Day Substance Use Urinalysis

Substance use will be assessed using urinalysis.

Time frame
Measured from baseline to 90-day follow-up.
4

Opioid-related knowledge and likelihood to engage in misuse behaviors

Opioid-related knowledge and likelihood to engage in misuse behaviors will be assessed with the Adolescent Opioid Safety and Learning scale. The Adolescent Opioid Safety and Learning Scale is a 16-item instrument comprising four separately scored subscales: Opioid Learning Interest (5 items; summed score range 5-25, with higher scores indicating greater interest in learning about opioid safety), Opioid Misuse Behavior Recognition (4 yes/no items; summed score range 0-4, with higher scores indicating better recognition of opioid misuse), Likelihood to Misuse Opioids (4 items; summed score range 4-20, with higher scores indicating a greater likelihood of opioid misuse and therefore a worse outcome), and Opioid Harm (3 items; summed score range 3-15, with higher scores indicating greater perceived harm from opioid misuse). The four subscales will be analyzed separately.

Time frame
Assessed from baseline to 90-day follow-up

Secondary outcomes

1

Motivation for substance use and problems associated

Motivation for substance use and problems associated will be measured with the Short Inventory of Problems

Time frame
Assessed between the baseline assessment and 90-day follow-up
2

Depressive Symptoms

Depressive symptoms will be assessed with the Patient Health Questionnaire-9. The Patient Health Questionnaire-9 is a 9-item self-report measure of depressive symptom severity during the preceding two weeks. Each item is scored from 0 ("not at all") to 3 ("nearly every day"). Item scores are summed to produce a total score ranging from 0 to 27. Higher scores indicate greater depressive symptom severity and therefore a worse outcome.

Time frame
Assessed between the baseline assessment and 90-day follow-up
3

Anxiety Symptoms

Anxiety symptoms will be measured with the Generalized Anxiety Disorder 7-item scale (GAD-7). The Generalized Anxiety Disorder is a 7-item self-report measure of anxiety symptom severity during the preceding two weeks. Each item is scored from 0 ("not at all") to 3 ("nearly every day"). Item scores are summed to produce a total score ranging from 0 to 21. Higher scores indicate greater anxiety symptom severity and therefore a worse outcome.

Time frame
Assessed from baseline to 90-day follow-up.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Maryland, College Park

Lead sponsor

National Institute on Drug Abuse (NIDA)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: