FostrSpace-CASA R61/R33
CASA and FostrSpace: Systems Delivery of Digital Substance Use Prevention Tools to Foster Youth
2 other identifiers
interventional
400
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2024
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2024
CompletedFirst Submitted
Initial submission to the registry
December 16, 2024
CompletedFirst Posted
Study publicly available on registry
March 13, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2029
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2029
March 13, 2025
March 1, 2025
5 years
December 16, 2024
March 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Rate of Drug Use
The Texas Christian University (TCU) drug screen with opioid supplement is used to gather detailed information about drug and opioid use.
baseline
Rate of Cigarette Use
The Cigarette smoking and vaping/e-cigarette use is used to gather detailed information about nicotine and/or cannabis use.
baseline
Secondary Outcomes (4)
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
Other Outcomes (16)
CASA Background Characteristics
baseline
Arrest and Treatment
baseline
Youth Background Characteristics
baseline
- +13 more other outcomes
Study Arms (2)
InfoECHO
EXPERIMENTALCASA volunteers will attend a six 90-minute/biweekly co-occurring SU and trauma ECHO trainings.
InfoOnly
OTHERCASA volunteers will attend a one-time 30-60 minute co-occurring SU and trauma ECHO training.
Interventions
Eligibility Criteria
You may qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UCSF Zuckerberg San Francisco General Hospital
San Francisco, California, 94131, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Marina Tolou-Shams, PhD
University of California, San Francisco
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 16, 2024
First Posted
March 13, 2025
Study Start
March 1, 2024
Primary Completion (Estimated)
March 1, 2029
Study Completion (Estimated)
March 1, 2029
Last Updated
March 13, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share