- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02152618
Kansas Intensive Permanency Project (PIIKIPP)
March 22, 2019 updated by: Westat
Permanency Innovations Initiative- Kansas Intensive Permanency Project
The intervention provides services to children with Serious Emotional Disturbance (SED) who are in foster care and to their parent(s) to prepare the families for reunification.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The intervention provide services to children with Serious Emotional Disturbance (SED) who are in foster care and to their birth parents to prepare the families for reunification.
The evaluation follows a randomized design.
The pretest will assess the procedures and instruments for collecting data on child, youth, and family functioning.
Ultimately, after the pretest is complete, the data collected through the evaluation will provide information on the extent to which the intervention achieved its goal of improving parenting skills and enhancing readiness for reunification among the families who received the services.
Study Type
Interventional
Enrollment (Actual)
1652
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
3 years to 16 years (CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Children age 3-16 with severe emotional disturbances
- In foster care and their families (parents).
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: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Treatment
|
Evidence-based, behavioral parent management training model, Parent Management Training - Oregon Model (PMTO) tailored to address permanency barriers of parents of children with SED.
|
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
|
Positive parenting behaviors
Time Frame: Pre intervention, post intervention and at 12-months
|
Measured by administering two standardized instruments: 1) the Caregiver Wish List (CWL); and, 2) the Family Interaction Task (FIT).
|
Pre intervention, post intervention and at 12-months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Use of community resources & social supports
Time Frame: Pre intervention, post intervention and at 12-months
|
Measured by observing the results of a subscale of a standardized instrument, the North Carolina Family Assessment Scale, General and Reunification services (NCFAS-G+R).
The subscale is identified as "social/community life."
|
Pre intervention, post intervention and at 12-months
|
Readiness for Reunification
Time Frame: Pre intervention, post intervention and at 12-months
|
Measured by the "readiness for reunification" subscale of the North Carolina Family Assessment Scale, General and Reunification services (NCFAS-G+R).
|
Pre intervention, post intervention and at 12-months
|
Improve parent mental health & Substance Abuse
Time Frame: Pre intervention, post intervention and at 12-months
|
Measured by the relevant items on the North Carolina Family Assessment Scale, General and Reunification services (NCFAS-G+R).
|
Pre intervention, post intervention and at 12-months
|
Child behavior
Time Frame: Intake & every 6-months post intake
|
Measured with Social Skills Improvement System rating scales (SSIS).
|
Intake & every 6-months post intake
|
Child functioning
Time Frame: Intake & every 6-months post intake
|
Measured by assessing the child's functioning with the Child and Adolescent Functional Assessment Scale (CAFAS) for school-aged children and the Preschool and Early Childhood Functional Assessment Scale (PECFAS) for preschool-aged children.
|
Intake & every 6-months post intake
|
Reunification
Time Frame: 18 months post intervention start date
|
Measured using data from Kansas' state administrative database for child welfare as reported to AFCARS/NCANDS.
|
18 months post intervention start date
|
Long-term foster care
Time Frame: Measured at 6 and 12 months post entry into foster care
|
Measured by using data from Kansas' state administrative database for child welfare as reported to AFCARS/NCANDS.
|
Measured at 6 and 12 months post entry into foster care
|
Stable permanency
Time Frame: Measured at 6 and 12 months post entry into foster care
|
Measured by using data from Kansas' state administrative database for child welfare as reported to AFCARS/NCANDS.
|
Measured at 6 and 12 months post entry into foster care
|
Child safety
Time Frame: Measured at 6 and 12 months post entry into foster care
|
Measured by using data from Kansas' state administrative database for child welfare as reported to AFCARS/NCANDS.
|
Measured at 6 and 12 months post entry into foster care
|
Coercive parenting practices
Time Frame: Pre intervention, post intervention and at 12-months
|
Measured by administering two standardized instruments: 1) the Caregiver Wish List (CWL); and, 2) the Family Interaction Task (FIT).
|
Pre intervention, post intervention and at 12-months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
November 1, 2015
Study Completion (Actual)
November 1, 2015
Study Registration Dates
First Submitted
April 14, 2014
First Submitted That Met QC Criteria
May 28, 2014
First Posted (Estimate)
June 2, 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
Additional Relevant MeSH Terms
Other Study ID Numbers
- HHSP23320095655WC-KS
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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