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Clinical Trials/NCT06875323
NCT06875323Enrolling By InvitationNot Applicable

CASA and FostrSpace: Systems Delivery of Digital Substance Use Prevention Tools to Foster Youth

University of California, San Francisco2 sites in 1 country400 target enrollmentStarted: March 1, 2024Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
400
Locations
2
Primary Endpoint
Rate of Drug Use

Study Overview

Brief Summary

The purpose of this study is to understand how an online digital health application (app) called FostrSpace can reduce substance use among youth (ages 13-20 years old) in foster care.

Detailed Description

The goal of this clinical trial is to identify gaps in substance use prevention across existing CASA trainings and the FostrSpace app for foster youth and test how substance use trainings for CASA volunteers could help facilitate FostrSace app referrals to reduce and prevent substance use among CASA youth.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
13 Years to 20 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adolescents and young adults will be eligible if they are age 13-20, are proficient in English, have an assigned CASA worker, and have a device with web access.
  • CASAs (ages 18 and over) will be eligible if they are assigned to a youth between the ages of 13- 20.

Exclusion Criteria

  • Youth: Exclusion criteria include being non-English speaking, being within 3 months of ending with CASA services, cognitive impairment that precludes ability to provide informed consent.
  • CASA: Exclusion criteria include being non-English speaking and working with a youth who is within 3 months of ending with CASA services.

Arms & Interventions

InfoOnly

Other

CASA volunteers will attend a one-time 30-60 minute co-occurring SU and trauma ECHO training.

Intervention: Informational Session (Other)

InfoECHO

Experimental

CASA volunteers will attend a six 90-minute/biweekly co-occurring SU and trauma ECHO trainings.

Intervention: ECHO-FostrSpace (Other)

Outcomes

Primary Outcomes

Rate of Drug Use

Time Frame: baseline

The Texas Christian University (TCU) drug screen with opioid supplement is used to gather detailed information about drug and opioid use.

Rate of Cigarette Use

Time Frame: baseline

The Cigarette smoking and vaping/e-cigarette use is used to gather detailed information about nicotine and/or cannabis use.

Secondary Outcomes

  • The Alcohol and Marijuana Expectancy Questionnaire(baseline)
  • The Brief Young Adult Alcohol Consequences Questionnaire(baseline)
  • The Brief Marijuana Consequences Questionnaire(baseline)
  • The Brief Symptom Inventory(baseline)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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