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The Impact of Parent Training on the Child's Health Services

Terminated
Conditions
Child Behavior Problem
Parenting
Child Rearing
Interventions
Behavioral: Video-Based Parent Training Program
Registration Number
NCT03704974
Lead Sponsor
Children's Hospital Los Angeles
Brief Summary

The purpose of the study is to determine whether parent training with the Incredible Years Parent Program delivered in pediatric primary care decreases usage of healthcare services for the next year when compared to annual healthcare service use during the two years prior to the parents participating in program.

Detailed Description

Pediatric health services utilization (pHSU) by children with mental health conditions demonstrated dramatic increases between 2006 and 2011. These national trends reflecting large increases in pHSU for mental health conditions were seen across multiple developmental levels. Health services costs for children with mental health conditions are estimated to be twice those for the average child. The Incredible Years® Parent Program (IY) has a strong evidence-base supporting its effectiveness in reducing early onset conduct problems. The overall objective of this stage 3 (T3) translational research proposal is to conduct a pilot study of 45 pediatrician-referred parents who participate in IY and examine the impact of IY on pHSU of their children. Pediatric HSU outcome measures include: all-cause ED visits; in-patient hospitalizations and length of stay; authorizations for specialist referrals; primary and acute care visits; and ED visits for mental health conditions. The investigator's central hypothesis is that children ages 3 to 6 years with behavior concerns whose parents are referred by their pediatricians for participation in IY will have decreased mean annual all-cause pHSU and decreased ED visits for mental health conditions in the 12 months following IY, compared to the 24 months prior to IY participation. This is important to demonstrate because significant financial barriers exist to integrating effective family focused prevention services like IY into pediatric primary care settings. Demonstration of reduced pHSU is one way to address these translational barriers. Results of this pilot study are expected to provide preliminary data on pre- and post-intervention effect sizes; these data will be used to demonstrate the feasibility of collecting data using existing sources of pHSU to design a more fully powered multi-site trial with a robust comparator group.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
7
Inclusion Criteria
  • Children receiving primary care at CHLA AltaMed with parent-reported behavioral concerns whose parents are referred by their pediatricians for participation in the Incredible Years Parenting Program.
  • Continuous enrollment in AltaMed Medicaid funded health services during the 24 months prior to participation in IY and 12 months following participation in IY with lapses in coverage of no more than 90 days in length.
  • Parents are English or Spanish-speaking or willing to use interpretation if they speak another language.
Exclusion Criteria
  • Private (commercial non-Medicaid) insurance coverage for greater than 90 days during the 24 months prior to participation in IY and 12 months following participation in IY.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Children of Parents Receiving IYVideo-Based Parent Training ProgramChildren ages 3 to 6 years at start of group with behavior concerns whose parents are referred by their pediatricians for participation in a video-based parent training program from 2014 through 2018.
Primary Outcome Measures
NameTimeMethod
Change in Annual Pediatric Health Services Utilization from 24 months prior to IY Parent Group Participation to 12 months following IY Parent Group ParticipationUtilization for 24 months prior to intervention and 12 months following intervention

(1) all-cause Emergency Department (ED) visits (yes/no) and number; (2) ED visits for mental health conditions (yes/no) and number; (3) in-patient hospitalizations (yes/no) and number, and length of stay in days; (4) authorizations for specialist referrals from AltaMed (yes/no) and number; (5) number of AltaMed primary care visits; (6) AltaMed acute care visits (yes/no) and number; (7) AltaMed mental health visits (yes/no) and number; (8) Children's Hospital Los Angeles (CHLA) specialty mental health visits (yes/no) and number.

Secondary Outcome Measures
NameTimeMethod
Youth Outcome Questionnaire (Parent Report)During week before or after starting group; and during week before or after ending group, up to 20 weeks

Total raw score \[measures change in frequency of child symptoms and prosocial behaviors; range -16 to 240; higher worse\].

Pediatric Symptom ChecklistDuring week before or after starting group; and during week before or after ending group, up to 20 weeks

Total raw score \[measures frequency of pediatric psychosocial problems; range 0 to 70; higher worse\].

Eyberg Child Behavior InventoryDuring week before or after starting group; and during week before or after ending group, up to 20 weeks

Raw and T-scores for Intensity \[measures frequency of problem behaviors; range 36 to 252; higher worse\] and Problem \[measures number of behaviors that are a problem for the parent; range 0 to 36; higher worse\] Subscales

Trial Locations

Locations (1)

Children's Hospital Los Angeles

🇺🇸

Los Angeles, California, United States

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