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Families Together: Intervention for Reunified Families

Intervention to Improve Outcomes for Foster Children Reunited With Their Birth Families

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04382677
Enrollment
264
Registered
2020-05-11
Start date
2017-12-20
Completion date
2025-01-31
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Child Abuse, Child Neglect

Keywords

Child Welfare, Child Protective Services, Parenting, Child maltreatment

Brief summary

Birth parents of young children who have been placed into foster care are a highly vulnerable population of caregivers. Little is known about the ability of existing prevention programs to intervene with birth parents who have recently been reunified with their children under the age of six. This project aims to evaluate a brief, home-visiting intervention model with a sample of reunified birth parents, examining its effectiveness to improve parenting and child wellbeing, and reduce reoccurrence of maltreatment and reunification failure.

Detailed description

There is no brief, home visiting, evidence-based intervention designed for and evaluated with Child Welfare System (CWS) birth parents and their children under six, once they are reunified. Why is this important? Because reunified birth parents represent one of the highest risk subpopulations of parents whose challenges contribute both to their child's exposure to stress and trauma and to the intergenerational transmission of impaired parenting, maltreatment, and foster care placement. Reunified birth parents are more likely than other parents to have been foster children and survivors of childhood maltreatment. They have higher rates of co-morbid mental health disorders, substance abuse, poverty, low education, and homelessness. When their children are placed in out-of-home care as infants or toddlers, they are more likely to have longer stays in foster care than any other age group. Foster children are at risk for serious emotional, behavioral, neurological, and physiological health problems, and for continued relationship disruptions, maltreatment, and foster care placements throughout their life course. Birth parents need intervention services when they reunite with their child to support the already fragile parent-child relationship. Even when birth parents work hard to fulfill court requirements to regain custody of their child, they are often left without the skills necessary to establish a strong and lasting connection with their child. This failure of service, we believe, leads reunified families to experience a high rate of maltreatment reoccurrence and reentry into foster care. In this application we will evaluate the effectiveness of a community based, home visiting intervention program with a population of birth parents recently reunified with their child under the age of six after a foster care placement. In order to do this, we first adapt the program by adding material relevant to reunified birth families and adapt the material for older children. We will evaluate the effectiveness of Promoting First Relationships ® (PFR; Kelly et al., 2008) to meet the parenting needs of this vulnerable population. Promoting First Relationships was originally designed for children birth to three, and we will expand the curriculum to meet the needs of children through age six. Through a strong, established community partnership between the state, a community mental health agency, and the University of Washington, we will 1) adapt Promoting First Relationships ® (PFR) for reunified birth families and older children; 2) test the effectiveness of PFR to improve parental quality and parent-child interaction as compared to a Resource and Referral service; 3) test the effectiveness of PFR on reducing social, emotional, and behavioral problems in a population of children at risk for elevated emotional and behavioral disorders; 4) test the effectiveness of PFR in reducing referrals to Child Protective Services (CPS) and re-entry into foster care. Participants complete baseline assessments during an observation-only period. The parent-child dyad is randomized following the baseline assessment. They then receive the study intervention for 7-43 weeks, after which no further intervention is delivered. Outcome assessments are conducted during the post-intervention follow-up period immediately after completion of the intervention and again 6 months later. Outcome assessments are obtained (if possible) even when the intervention is not completed, for intent-to-treat analyses.

Interventions

BEHAVIORALPromoting First Relationships ®

Promoting First Relationships ® is based on attachment theory and is strengths-based. The 12 week intervention is delivered in the home of the family. Each week has a theme for discussion, handouts, an activity, and time for "joining" - checking in with the parent, listening to their concerns, and establishing a positive, supportive relationship. The provider videotapes playtime between parent and child, and alternates weeks watching the video with the parent, reflecting about the needs of both parent and child (reflective observation). PFR consultation strategies include Joining, Positive Feedback, Instructive Feedback, Reflective Questions and Comments, and Instruction with Handouts. These core strategies enhance parents' sense of security and competency. The provider helps the parent develop greater empathy and understanding of the child's needs and feelings, and helps the parent to identify their own feelings and needs around parenting.

OTHERResource & Referral

This condition consists of 1) Resource \& Referral assistance provided over the phone, and 2) Local Services Resource Packet. Throughout the intervention period, the provider makes monthly phone calls to offer further support to families, answer questions, and provide additional resources. The provider has at least four interactions with each family served. In addition, families in this condition have the Resource and Referral Specialist's phone number and they can call if an additional need arises. The resource packet includes local information organized by type of need or resource. These packets are updated regularly as services change over time.

Sponsors

University of Washington
Lead SponsorOTHER
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Birth parents reunited with their child (age 1-5 years) after a foster or kin care placement in trial return home status * Parenting the child at study enrollment * Child Welfare case served by the following Washington State offices: all of Region 2 South, Lynnwood, Tacoma, Everett, Smokey Point, and Lakewood * Birth parents must be age 18 or older, mothers and fathers are eligible (one parent per study child enrolled) * Conversant in English * Access to a telephone * Housing situation allows for home visits

Exclusion criteria

* Experiencing an acute crisis (e.g., hospitalization, incarceration) * Previously received the Promoting First Relationships ® intervention or Child Parent Psychotherapy (CPP)

Design outcomes

Primary

MeasureTime frameDescription
Child Welfare Services Removal From Birth Parent Home18 months post enrollment in the studyOfficial child welfare administrative records indicating whether the child in they dyad was removed from the birth parent home. 18 months post enrollment is approximately 1 year post intervention for those who completed interventions on schedule
Change in Parental Sensitivity (Video Recorded Observations Coded by Coders Blind to Intervention)Post intervention (Time 2) -- approximately 6 months after Baseline (Time 1)Parent sensitivity is measured by the Nursing Child Assessment Teaching Scale (NCATS; Barnard 1994), a videotaped interaction to assess caregiver sensitivity, stimulation of the child, and emotional responsiveness during interaction. The score is the sum of 37 items, ranging from 0 to 37; higher scores indicate greater parental sensitivity.
Change in Parenting Knowledge of Child DevelopmentPost intervention (Time 2) -- approximately 6 months after Baseline (Time 1)14-item Likert-scale questionnaire developed by the study, "Raising a Child," is a measure of caregivers' knowledge of children's social-emotional needs and developmentally appropriate expectations. Items are scored on a scale ranging from 1 to 4 points. The Raising a Child scale score is the sum of the 14 items; the range is 14 to 56 with higher scores indicating greater parenting knowledge (better outcome).

Secondary

MeasureTime frameDescription
Change in Child Externalizing Problem BehaviorPost intervention (Time 2) -- approximately 6 months after Baseline (Time 1)Child externalizing behavioral problems will be measured based on parent report using the Child Behavior Check List (CBCL: Achenbach \& Rescorla, 2000). The externalizing scale has 24 items; raw scores can range from 0 to 48 with higher scores indicating more externalizing behaviors.
Change in Child Internalizing Problem BehaviorPost intervention (Time 2) -- approximately 6 months after Baseline (Time 1)Child internalizing behavioral problems will be measured based on parent report using the Child Behavior Check List (CBCL: Achenbach \& Rescorla, 2000). The internalizing scale has 36 items; raw scores can range from 0 to 72 with higher scores indicating more internalizing behaviors.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMonica L Oxford, MSW, PhD

University of Washington

Participant flow

Recruitment details

Recruitment took place between 12/2017 and 5/2023 in collaboration with the Washington State Department of Children, Youth, & Families (DCYF). A DCYF study liaison mailed opt-out letters to birth parents recently reunified with a child aged 1-5 years after a foster care placement (open case in Trial Return Home status), living in the greater Seattle, WA area. Parents who did not opt out were contacted by a study recruiter, screened for eligibility, and enrolled in the study.

Pre-assignment details

Of the eligible parent-child dyads (N=427), 264 dyads enrolled:1 parent and 1 child each equating to 528 total parent and child participants.

Baseline characteristics

Characteristic
Age, Continuous
Children
2.542 Years
STANDARD_DEVIATION 1.389
Age, Continuous
Parents
31.99 Years
STANDARD_DEVIATION 6.162
Dyad enrolled relative to COVID-19 pandemic
Enrolled after COVID-19 pause
47 dyads
Dyad enrolled relative to COVID-19 pandemic
Enrolled prior to COVID-19
85 dyads
Ethnicity (NIH/OMB)
Children
Hispanic or Latino
25 Participants
Ethnicity (NIH/OMB)
Children
Not Hispanic or Latino
106 Participants
Ethnicity (NIH/OMB)
Children
Unknown or Not Reported
0 Participants
Ethnicity (NIH/OMB)
Parents
Hispanic or Latino
28 Participants
Ethnicity (NIH/OMB)
Parents
Not Hispanic or Latino
116 Participants
Ethnicity (NIH/OMB)
Parents
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Children
American Indian or Alaska Native
5 Participants
Race (NIH/OMB)
Children
Asian
0 Participants
Race (NIH/OMB)
Children
Black or African American
11 Participants
Race (NIH/OMB)
Children
More than one race
85 Participants
Race (NIH/OMB)
Children
Native Hawaiian or Other Pacific Islander
1 Participants
Race (NIH/OMB)
Children
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Children
White
142 Participants
Race (NIH/OMB)
Parents
American Indian or Alaska Native
6 Participants
Race (NIH/OMB)
Parents
Asian
1 Participants
Race (NIH/OMB)
Parents
Black or African American
14 Participants
Race (NIH/OMB)
Parents
More than one race
21 Participants
Race (NIH/OMB)
Parents
Native Hawaiian or Other Pacific Islander
3 Participants
Race (NIH/OMB)
Parents
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
Parents
White
83 Participants
Sex: Female, Male
Children
Female
62 Participants
Sex: Female, Male
Children
Male
70 Participants
Sex: Female, Male
Parents
Female
109 Participants
Sex: Female, Male
Parents
Male
25 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 1320 / 1321 / 1320 / 132
other
Total, other adverse events
0 / 1320 / 1320 / 1320 / 132
serious
Total, serious adverse events
0 / 1320 / 1321 / 1320 / 132

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 15, 2026