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

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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