Summary

Eligibility
for people ages 12 years and up (full criteria)
Location
at San Francisco, California
Dates
study started
completion around
Principal Investigator
by Marina Tolou-Shams, PhD
Headshot of Marina Tolou-Shams
Marina Tolou-Shams

Description

Summary

The purpose of this research is to adapt and evaluate the efficacy of an existing family based intervention to be delivered via telehealth to child welfare-involved (CWI) youth and their caregiver of origin.

Official Title

Leveraging Technology to Improve Family Relationships for Adolescents in Out-of-Home Placement

Details

The goal of this study is to adapt and evaluate the efficacy of an existing empirically supported, family-based affect management intervention to be delivered via telehealth. There are two versions of this intervention: 1) a dyadic version to be delivered to CWI youth and their caregiver of origin, and 2) a caregiver-only version to be delivered to any caregiver (including kinship caregivers) of a CWI youth. The study involves iteratively adapting the intervention with feedback from youth and caregiver participants and stakeholder partners, as well as evaluating the feasibility, acceptability, and preliminary effectiveness of the intervention.

Keywords

Parent-Child Relations, Communication, telehealth, parent-child relationships, adolescent, Quality communication, Housing stability, Child welfare, Emotional regulation, Family-based Telehealth Intervention

Eligibility

Location

  • UCSF Zuckerberg San Francisco General Hospital accepting new patients
    San Francisco California 94131 United States

Lead Scientist at UCSF

  • Marina Tolou-Shams, PhD
    Dr. Tolou-Shams is the Kilroy Realty Professor of Psychiatry and Vice Chair of Community Engagement, Outreach and Advocacy in the Department of Psychiatry and Behavioral Sciences (DPBS) at UCSF. She is also Deputy Vice Chair for Research in the DPBS at Zuckerberg San Francisco General Hospital (ZSFG).

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT04488523
Study Type
Interventional
Participants
Expecting 300 study participants
Last Updated