Preventing Conduct Disorder in Child Welfare

NCT ID: NCT03329625

Last Updated: 2017-11-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

144 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-07-05

Study Completion Date

2015-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

A mixed methods randomized control trial was conducted to test the effectiveness of Pathways Triple P with child welfare involved families compared to treatment as usual. Outcomes tested included parenting behaviors and attitudes, and child behavior problems. 144 families were recruited into the study. Data was collected at 4 time points (baseline, 4 months, 9 months, and 18 months). Over 70% were retained from baseline to 18 months.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Behavioral Disorder Child Maltreatment

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Triple P RCT parent management training Child welfare child behavior problems

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Pathways Triple P

Families randomized to the Pathways Triple P received a 14 week home based intervention.

Group Type EXPERIMENTAL

Pathways Triple P

Intervention Type BEHAVIORAL

Pathways Triple was developed by Matt Sanders and is a behavioral parent training intervention designed to treat child behavior problems and prevent child maltreatment.

Services as Usual

Families randomized to the services as usual condition received services as usual through the Missouri Children's Division

Group Type ACTIVE_COMPARATOR

Services as Usual

Intervention Type BEHAVIORAL

Families received family centered services and other parenting interventions as deemed appropriate by the child welfare case manager.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Pathways Triple P

Pathways Triple was developed by Matt Sanders and is a behavioral parent training intervention designed to treat child behavior problems and prevent child maltreatment.

Intervention Type BEHAVIORAL

Services as Usual

Families received family centered services and other parenting interventions as deemed appropriate by the child welfare case manager.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Families with open child protective service case following allegation of child physical abuse or neglect
* parent of child between the age of 3 and 12
* Child remained in the home following investigation
* parent spoke English

Exclusion Criteria

* parent's child could not have chronic medical condition or have a pervasive developmental delay
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Washington University School of Medicine

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Patricia Kohl, Ph.D.

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Patricia Kohl, PhD

Role: PRINCIPAL_INVESTIGATOR

Washington University School of Medicine

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

5R01HD061454

Identifier Type: NIH

Identifier Source: org_study_id

View Link