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Family Telehealth Project for Foster Care Youth

University of California San Francisco (UCSF) logo

University of California San Francisco (UCSF)

Status

Completed

Conditions

Parent-Child Relations
Communication

Treatments

Behavioral: Family-based Telehealth Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT04488523
1928922

Details and patient eligibility

About

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.

Full description

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.

Enrollment

93 patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Eligible youth:

  • Will be between the ages of 12 and 18 years
  • Will have ongoing child welfare involvement
  • Will be proficient in English
  • Will have no cognitive impairment which would preclude provision of informed assent

Eligible caregivers for dyadic version:

  • Will be the caregiver of origin for the enrolled youth
  • Will be proficient in English or Spanish
  • Will be cognitively capable of providing informed consent for themselves and their youth

Eligible caregivers for caregiver-only version:

  • Will be the caregiver of a youth, between the ages of 12 and 18 years, with ongoing child welfare involvement
  • Will be proficient in English or Spanish
  • Will have no cognitive impairment which would preclude provision of informed consent

Exclusion criteria

  • Caregivers whose rights were terminated due to substantiated abuse or neglect.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

93 participants in 1 patient group

Family-based Telehealth Treatment
Experimental group
Description:
A family-based telehealth intervention.
Treatment:
Behavioral: Family-based Telehealth Intervention

Trial contacts and locations

1

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Central trial contact

Johanna Folk; Marina Tolou-Shams, PhD

Data sourced from clinicaltrials.gov

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