RECRUITING

Delivering Evidence-Based Parenting Services to Families in Child Welfare Using Telehealth

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 goal of this randomized controlled trial is to compare Promoting First Relationships - Home Visit (PFR-HV) to Promoting First Relationships - Telehealth (PFR-T) among parents of 6-12 month olds in the child welfare system. The main questions it aims to answer are: * Is PFR-T effective relative to PFR-HV and Usual Care with respect to observed parent sensitive and responsive care, parent knowledge of child social and emotional development, and child externalizing behavior? * Is PFR-T effective relative to PFR-HV and Usual Care with respect to child out-of-home placement in foster care relative to the control group? * How does PFR-T compare in a benefit-cost analysis to the cost-effectiveness relative to PFR-HV and Usual Care? * Are eligible families impacted by the lack of technology and Wi-Fi/cellular data to engage in PFR-T? * How does provider adherence and fidelity in delivery of PFR-T compare to adherence and fidelity of PFR-HV? What will participants be asked to do? 1. Participants will be asked to agree to randomization, resulting in their placement in one of three groups: PFR-HV, PFR-T, or the control group. 2. Participants will be asked to participate in three virtual research visits, over the course of approximately 12 months (families could be finished as early as 9 months, however in our experience, intervention sessions and research visits often need to be rescheduled, delaying completion of the study). The research visits take approximately 80 minutes, and families will be paid $75 for each visit they participate in. 3. During the research visit, the families will be asked to participate in videotaped research activities involving parent-child play and interaction. Parents will be asked to answer questions regarding their background, feelings, parenting opinions, and stress. 4. Families randomized to the PFR-HV intervention are asked to participate in a 10 week in home parenting program which includes videotaped caregiver-child interactions and feedback. 5. Families randomized to the PFR-T intervention are asked to participate in a 10-week parenting program that will occur over Zoom, which will include videotaped caregiver-child interactions and feedback. 6. Families randomized to the control group will be emailed a resource packet with some information about services or programs that might be helpful for them.

Official Title

Delivering Evidence-Based Parenting Services to Families in Child Welfare Using Telehealth

Quick Facts

Study Start:2023-10-12
Study Completion:2028-04-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06109766

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. they are listed in the official DCYF child welfare database as having an open CPS investigation and a child listed in the case file who is between 6-12 months old,
  2. 2. they speak English,
  3. 3. they are not currently experiencing an acute hospitalization or incarceration,
  4. 4. they have the technological capacity to engage in telehealth, and
  5. 5. they have not had PFR in the past.
  1. 1. they are experiencing an acute crisis (e.g., hospitalization, incarceration),
  2. 2. they don't have stable enough housing to be able to have home visits,
  3. 3. they don't have reliable access to internet or cell service and/or a device with a microphone and camera,
  4. 4. previously received the Promoting First Relationships ® intervention or Child Parent Psychotherapy (CPP).

Contacts and Locations

Study Contact

Kristin Klansnic
CONTACT
206-519-7330
klansnic@uw.edu

Principal Investigator

Monica Oxford, PhD, MSW
PRINCIPAL_INVESTIGATOR
University of Washington

Study Locations (Sites)

University of Washington
Seattle, Washington, 98195
United States

Collaborators and Investigators

Sponsor: University of Washington

  • Monica Oxford, PhD, MSW, PRINCIPAL_INVESTIGATOR, University of Washington

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 Date2023-10-12
Study Completion Date2028-04-12

Study Record Updates

Study Start Date2023-10-12
Study Completion Date2028-04-12

Terms related to this study

Keywords Provided by Researchers

  • Telehealth
  • Fidelity
  • Cost-Benefit Analysis

Additional Relevant MeSH Terms

  • Parenting
  • Parent-Child Relations
  • Child Behavior
  • Child Maltreatment