Executive Function and Parenting in Childhood

NCT ID: NCT06241300

Last Updated: 2024-12-05

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-20
• Study Completion Date: 2028-03-31

Brief Summary

Deficits in executive functioning (EF) disproportionately impact children living in poverty and increase risk for psychopathology, particularly disruptive behavior disorders. This randomized clinical trial seeks to determine whether childhood EF, assessed across neural and behavioral units of analysis, is an experimental therapeutic target that can be directly modified through caregiver participation in the Chicago Parent Program (CPP), if increases in EF predict reduced disruptive behavior trajectories in low-income children over a short-term follow-up period, and identify which CPP-driven parenting skill improvements are the most influential in modifying EF. This work will contribute new knowledge as to whether a cost-efficient parenting intervention, developed for and with low-income families raising young children in poverty, can modify EF, a neural behavioral mechanism implicated in risk for childhood disruptive behavior problems.

Detailed Description

Impairments in executive functioning (EF), cognitive processes that support self-regulation, disproportionately impact children living in poverty and increase vulnerability for childhood disruptive behavior, which trigger a cascade of mental health problems and psychosocial difficulties across the lifespan. Poverty-related stress and maladaptive parenting styles have been linked to alterations of neural and behavioral EF markers in children; despite this, no studies have studied if parenting prevention programs can directly target childhood EF, and through improving EF, reduce disruptive behaviors in at-risk children. The National Institute of Mental Health (NIMH) funded K23 Mentored Patient-Oriented Research Career Development Award project seeks to conduct a mechanistic randomized clinical trial to determine whether neural-behavioral indices of childhood EF is an experimental therapeutic target that can be modified via caregiver participation in the Chicago Parent Program. Consistent with the NIMH Research Domain Criteria framework, childhood EF will be assessed across brain and behavior measurement units. The second aim of the clinical trial seeks to evaluate whether increases in childhood neural-behavioral EF mediate the effects of CPP in reducing disruptive behavior problems over a short-term follow-up. A third exploratory aim of the project is to preliminarily test whether increases in specific parenting practices (discipline, scaffolding), previously linked to individual differences in EF, mediate the effects of CPP in predicting change in childhood neural-behavioral EF. The sample will include 90 Medicaid eligible parent-child (ages 4-5 years old) dyads and will employ a novel recruitment approach where the target child will have moderate-to-severe EF delays at baseline but does not meet diagnostic criteria for a disruptive behavior disorder.

Conditions

Disruptive Behavior Disorder, Childhood Onset; Disruptive Behavior; Executive Function

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: SINGLE

Study Groups

Chicago Parent Program

Half of the dyads will be randomized to participant in the Chicago Parent Program (CPP), an evidence-based parenting preventive intervention for urban poor parents with children between the ages of 2-8 with behavior problems. The Chicago Parent Program consists of 12 groups sessions (11 weekly, 1 booster session). The groups are co-facilitated by two certified group leaders. Parents learn positive parenting and effective child behavior management skills, strategies to support the child's attention, literacy, and social skills, and stress management and problem solving techniques. Skill building is accomplished through watching videos of real-life parents and children during parent-child interactions, group discussion, role-playing, and weekly homework assignments.

Group Type: EXPERIMENTAL

Chicago Parent Program

Intervention Type: BEHAVIORAL

Chicago Parent Program is an evidence-based group parenting intervention designed to reduce disruptive behavior in young children (2-8 years old).

Control Condition

Half of the dyads will be randomized to the no intervention arm.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Chicago Parent Program

Chicago Parent Program is an evidence-based group parenting intervention designed to reduce disruptive behavior in young children (2-8 years old).

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Children must be between the ages of 4 years old and 5 years, 11 months old
• Parent must be the legal guardian of the target child and must live with the child full-time
• Parents will be 18 years and older (no maximum age limit)
• Only one child and one parent per family can participate in the study
• Child is Medicaid eligible, defined as receiving Medicaid or eligible based on family income (up to 142 percent of the federal poverty level)
• At enrollment the child will have moderate-to-severe (i.e., (sub)clinical) impairments in executive functioning as indicated by having a global executive composite standardized score greater than or equal to 60 on the Behavior Rating Inventory of Executive Function-Preschool Version (BRIEF-P), which will be completed by parents at the initial screen
• Given that some assessment materials are only validated in English, parents and children for this study will need to be English-speaking
• Child does not have a prior or current diagnosis of a disruptive behavior disorder based on Diagnostic Statistical Manual, Fifth Edition (DSM-5) criteria
• Child is not currently receiving mental health services
• Child does not take medications to treat emotional or behavioral problems
• Child does not have a medical condition, such as epilepsy, that would interfere with the completion of study tasks
• Child is not actively suicidal
• Child does not have a history of psychosis or currently psychotic
• Parent does not have a medical condition that would interfere with the completion of the study
• Parent does not have an intellectual disability that would interfere with their ability to complete the study
• Parent does not have a severe mental illness, active suicidal ideation, or current alcohol/substance abuse/dependence that would interfere with their ability to participate in the study
• Child can have a current or past histories of psychiatric disorders (anxiety, mood, attention deficit hyperactivity disorder)
• Parent can have current or past history of psychiatric disorders
• Parent can be taking medications to treat mental health problems

Exclusion Criteria

• Child is not between the ages of 4-5 years old
• The parent is not the legal guardian of the target child
• The parent does not live with the child full-time
• The parent is younger than 18 years old
• Child is not receiving Medicaid or Medicaid eligible
• Child does not have (sub)clinical impairments in executive functioning as indicated by having a global executive composite standardized score greater than or equal to 60 on the BRIEF
• Child and parent are not English-Speaking
• Child has a prior or current diagnosis of a disruptive behavior disorder based on DSM-5 criteria
• Child is currently receiving mental health services
• Child currently takes medications to treat emotional or behavioral problems
• Child has a medical condition, such as epilepsy, that would interfere with the completion of study tasks
• Child is actively suicidal
• Child has a history of psychosis or is currently psychotic
• Parent is not willing to be randomly assigned to receive the Chicago Parent Program intervention or to the control condition where they will not receive an intervention
• Parent has a medical condition that would interfere with the completion of the study
• Parent has an intellectual disability that would interfere with their ability to complete the study
• Parent has a severe mental illness and/or active suicidal ideation

• Minimum Eligible Age: 4 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Institute of Mental Health (NIMH)

NIH

Sponsor Role: collaborator

National Institutes of Health (NIH)

NIH

Sponsor Role: collaborator

University of Illinois at Chicago

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University of Illinois-Chicago

Chicago, Illinois, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Jennifer Suor, PhD

Role: CONTACT

Phone: 7733208989

Email: jesuor@uic.edu

Facility Contacts

Jennifer Suor, PhD

Role: primary

Jennifer Suor, PhD

Role: backup

Other Identifiers

K23MH130724-01A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2023-0048

Identifier Type: -

Identifier Source: org_study_id