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Enrolling by invitation NCT06875323

FostrSpace-CASA R61/R33

No phase Interventional Substance Use

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: ECHO-FostrSpace, Informational Session.
Who it may be relevant to
Registry conditions: Substance Use. Basic parameters: 13 years — 20 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 →
Official title

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

Overview

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.

Interventions

  • Other ECHO-FostrSpace
    Six ECHO-FostrSpace session training for CASA volunteers.
  • Other Informational Session
    One ECHO-FostrSpace session training for CASA volunteers.

Primary outcome measures

  • Rate of Drug Use [Time frame: baseline]
  • Rate of Cigarette Use [Time frame: baseline]
Secondary outcome measures (4)
  • The Alcohol and Marijuana Expectancy Questionnaire [Time frame: baseline]
  • The Brief Young Adult Alcohol Consequences Questionnaire [Time frame: baseline]
  • The Brief Marijuana Consequences Questionnaire [Time frame: baseline]
  • The Brief Symptom Inventory [Time frame: baseline]

Eligibility criteria

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.

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
Prevention

Study locations

United States · 1 center
  • UCSF Zuckerberg San Francisco General Hospital — San Francisco

Identifiers

NCT: NCT06875323 · 1R61DA059860-01 · R61DA059860

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗