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Search / Trial NCT06875323

FostrSpace-CASA R61/R33

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Mar 7, 2025

Trial Information

Current as of April 22, 2025

Active, not recruiting

Keywords

Foster Youth Substance Use M Health

ClinConnect Summary

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.

Gender

ALL

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.

Trial Officials

Marina Tolou-Shams, PhD

Principal Investigator

University of California, San Francisco

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

San Francisco, California, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported