- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02173314
Nevada Initiative to Reduce Long-Term Foster Care
March 22, 2019 updated by: Westat
Permanency Innovations Initiative- Nevada Initiative to Reduce Long-Term Foster Care
The evaluation of the Nevada Initiative to Reduce Long-Term Foster Care (LTFC) includes three populations.
It will examine how the interventions SAFE- FC and FSE impact or relate to permanency outcomes for children most at risk for long term foster care and currently in care.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The project targets three populations of children.
For populations 1 and 2, the study will evaluate an intervention known as SAFE-FC.
The intervention aims to prevent long term foster care by providing tailored services and intensive engagement with all new families with children identified as unsafe (Population 1) and for cases that are currently in care and at risk of LTFC where reunification is the case goal (Population 2).
Family Search and Engagement (FSE) is the intervention for Population 3; it involves intense search practices to identify possible permanency resources.
For Populations 1 and 2 the study is a randomized, intent-to-treat design to measure safety and permanency outcomes.
For Population 3 the evaluation will be a descriptive study to analyze relationships between the intervention approach and outcomes.
Both studies aim to examine how the interventions (SAFE- FC and FSE) impact or relate to permanency outcomes for children most at risk for long term foster care.
Study Type
Interventional
Enrollment (Actual)
507
Phase
- Not Applicable
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.
Eligibility Criteria
Ages Eligible for Study
No older than 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Children assessed to be unsafe via the Nevada Initial Assessment
- children in foster care with specific risk characteristics.
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment
|
SAFE - FC, a combination of SAFE (developed by ACTION for Child Protection) and Family Connections (developed by Ruth H. Young Center for Families and Children, University of Maryland School of Social Work) for Populations 1 and 2.
Other Names:
|
|
No Intervention: Comparison
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time to stable permanence
Time Frame: Measured from the date of random assignment to the discharge date or to the end of the study period for cases that did not discharge
|
Measured by administrative data from the Adoption and Foster Care Analysis and Reporting System (AFCARS)
|
Measured from the date of random assignment to the discharge date or to the end of the study period for cases that did not discharge
|
|
Caregiver readiness for change
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Measured with Readiness for Parenting Change Scale (REDI) Abbreviated (Chaffin et al, 2011)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Caregiver stress
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Parenting Stress Index - Short Form (PSI-SF) (Abidin, 1983)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Caregiver mental health
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Brief Symptoms Inventory (BSI) (Derogatis, 1993)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
|
Child behavior/mental health problems
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Child Behavior Checklist (CBCL) (Achenbach, 1991)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
|
Positive parenting attitudes
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Adult-Adolescent Parenting Inventory (AAPI-2) (Bavolek & Keene, 1999)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
|
Social support
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Social Provisions Scale (SPS) (Russell & Cutrona, 1984)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
|
Helping alliance for both caregiver and worker
Time Frame: Measured at 6 months and again at case closure (duration of their involvement with Washoe County DSS is on average 24 months)
|
Helping Relationship Inventory (Poulin & Young, 1997)
|
Measured at 6 months and again at case closure (duration of their involvement with Washoe County DSS is on average 24 months)
|
|
Resiliency
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Resiliency Attitudes Scale (RAS) (Briscoe, B. & Harris, B., 1994)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
|
Home stability
Time Frame: Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
Based on subscales of the CWBS (questions from Zuravin & DePanfilis, 1996)
|
Measured at intake, at 6 months, 12 months, 18 months, and again at case closure (participants will be followed throughout the duration of their involvement with Washoe County DSS which is on average 24 months)
|
|
Time to permanency
Time Frame: Measured every six months in calendar year
|
State administrative data system
|
Measured every six months in calendar year
|
|
Recurrence of child abuse and neglect
Time Frame: Measured every six months in calendar year
|
State administrative data system
|
Measured every six months in calendar year
|
|
Placement rate (population 1 only)
Time Frame: Measured every six months in calendar year
|
State administrative data system
|
Measured every six months in calendar year
|
|
Time for case closure
Time Frame: Measured every six months in calendar year
|
State administrative data system
|
Measured every six months in calendar year
|
|
Time to reunification
Time Frame: Measured every six months in calendar year
|
State administrative data system
|
Measured every six months in calendar year
|
|
Foster care re entry rate
Time Frame: Measured every six months in calendar year
|
State administrative data system
|
Measured every six months in calendar year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 Major Dates
Study Start
September 1, 2010
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
December 1, 2015
Study Registration Dates
First Submitted
June 17, 2014
First Submitted That Met QC Criteria
June 23, 2014
First Posted (Estimate)
June 24, 2014
Study Record Updates
Last Update Posted (Actual)
March 26, 2019
Last Update Submitted That Met QC Criteria
March 22, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 8977-2
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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