COMPLETED

Family Telehealth Project for Foster Care Youth

Conditions

Parent-Child Relations Communication telehealth parent-child relationships adolescent Quality communication Housing stability Child welfare Emotional regulation

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Quick Facts

Study Start:2019-07-01

Study Completion:2025-11-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT04488523

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD, ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* 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 * 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 * 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	* Caregivers whose rights were terminated due to substantiated abuse or neglect.

Inclusion Criteria

Exclusion Criteria

* 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
* 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
* 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

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

Contacts and Locations

Principal Investigator

Marina Tolou-Shams, PhD

PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Study Locations (Sites)

UCSF Zuckerberg San Francisco General Hospital

San Francisco, California, 94131

United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

Marina Tolou-Shams, PhD, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-07-01

Study Completion Date2025-11-01

Study Record Updates

Study Start Date2019-07-01

Study Completion Date2025-11-01

Terms related to this study

Keywords Provided by Researchers

telehealth
parent-child relationships
adolescent
Quality communication
Housing stability
Child welfare
Emotional regulation

Additional Relevant MeSH Terms

Parent-Child Relations
Communication