About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- Chicago Parent Program
Treatment groups
Sponsors and collaborators
University of Illinois at Chicago
Lead sponsor
National Institute of Mental Health (NIMH)
Collaborator
National Institutes of Health (NIH)
Collaborator