Parent Preferences and Family Engagement in a Conduct Problems Prevention Program

Conduct Problems Clinical Trial

Official title:

DCISR for Adaptive Intervention Models in Children's Mental Health

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02432014
• Other study ID #: 1006S83774
• Secondary ID: P20MH085987
• Status: Completed
• Phase: N/A
• Start date: January 2012
• Est. completion date: September 2015

Study information

• Verified date: October 2019
• Source: University of Minnesota
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to gain a better understanding of family preferences for and engagement in services.

Description:

The overarching goal of this pilot project is to elucidate factors that influence families' engagement in indicated prevention/early intervention programming for youth conduct problems. We will explore factors previously shown to influence engagement, including parent motivational cognitions, family context variables, and preferences for intervention type. Study aims are organized around a randomized preference trial with a parallel hybrid design structure (see Abikoff, 2001). Families with youth ages 5-12, referred to community mental health clinics in Michigan, will be invited to participate in a prevention study. Families who chose to participate were assigned at random to preference (i.e. choice) or no preference (i.e. no choice) conditions. Those randomly assigned to the preference condition were allowed to choose between four intervention options: clinic-based services-as-usual (youth intervention); individual, home-based Oregon Parent Management Training (PMTO; Patterson, 2005), individual, clinic-based PMTO, and in-person group-based PMTO (Parenting Through Change; Forgatch & DeGarmo, 1999). Families in the no-choice condition were randomly assigned to one of the same four conditions.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 134
• Est. completion date: September 2015
• Est. primary completion date: July 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 5 Years to 12 Years

Eligibility

Inclusion Criteria:

• Families with at least one child between the ages of 5 and 12.

• Referral to community mental health clinic (specifically, to one of the project partner clinics)

Exclusion Criteria:

• Active psychosis

• Serious child mental health diagnosis

• Open child protection case for abuse or neglect

Related Conditions & MeSH terms

• Conduct Problems

Intervention

Behavioral:
• PMTO-PTC Group clinic-based

• PMTO Individual home-based

• PMTO Individual clinic-based

• Services as Usual

Locations

Country	Name	City	State
United States	Center for Personalized Prevention Research in Children's Mental Health	Minneapolis	Minnesota

Sponsors (3)

Lead Sponsor	Collaborator
University of Minnesota	Michigan Department of Community Health, National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Family Interaction Task (FIT)	Parent(s) and child participate in a number of activities which are observed and coded based on parent-child interactions.	1 year
Primary	Strengths and Difficulties Questionnaire	Parent and Teacher Report	1 year
Primary	Brief Symptom Inventory 18 (BSI-18) Questionnaire	Parent Report	1 year
Primary	Perceptions of Intervention Benefits and Barriers Questionnaire	Parent Report	1 year
Primary	Parent Locus of Control Questionnaire	Parent Report	1 year
Primary	Perceived Susceptibility & Severity Questionnaire	Parent Report	1 year
Primary	Perceived Need to Improve Parenting Questionnaire	Parent Report	1 year
Primary	Child Service Utilization Summary Questionnaire	Parent Report	1 year