Skip to main content
Clinical Trials/NCT02709291
NCT02709291
Completed
Not Applicable

Systematically Adapted Delivery of the Family Check-Up in Underserved Communities

Christina Studts1 site in 1 country51 target enrollmentFebruary 20, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parenting, Child Behavior, Implementation
Sponsor
Christina Studts
Enrollment
51
Locations
1
Primary Endpoint
Feasibility: Enrollment
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Early childhood disruptive behavior problems lead to significant costs to families and society, but can be reduced with behavioral parent training interventions. To increase the public health impact of these interventions, their feasibility, accessibility, and acceptability in high-need, underserved communities must be ensured. This pilot project will systematically adapt and pilot-test the delivery model of an existing effective parent training intervention for implementation in rural Appalachia, a region with many documented health disparities, high levels of poverty, and shortages of mental health providers. Community health workers in 5 rural Appalachian counties will be trained to deliver a behavioral parent training intervention. Each worker will deliver the intervention to 4 parent-child dyads.

Registry
clinicaltrials.gov
Start Date
February 20, 2017
End Date
June 26, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Christina Studts
Responsible Party
Sponsor Investigator
Principal Investigator

Christina Studts

Assistant Professor

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • Parents: aged 18+ years, custodial guardian of child, can speak/read/understand English
  • Children: ages 3-5 years, lives full time in custodial guardian's home
  • Community health workers: aged 18+ years, currently employed at a partnering health department, able to speak/read/understand English

Exclusion Criteria

  • Parents: has already accessed behavioral health services for the child, reports suicidal ideation or intent to harm self or others, participated in formative research for this study
  • Children: diagnosed with a severe developmental condition (i.e., significant developmental delay, autism, debilitating neurological condition)
  • Community health workers: none

Outcomes

Primary Outcomes

Feasibility: Enrollment

Time Frame: 2 weeks after final parent-child dyad completes the study

Percentage of invited parents who enroll in the study (obtained from process records)

Secondary Outcomes

  • Interventionist satisfaction(2 weeks after final parent-child dyad completes study)
  • Interventionist evidence-based practice attitudes(2 weeks after final parent-child dyad completes study)
  • Interventionist self-efficacy(2 weeks after final parent-child dyad completes study)
  • Feasibility: Number of sessions completed(2 weeks after final parent-child dyad completes the study)
  • Feasibility: Interventionist-reported fidelity(following each behavioral parent training intervention session)
  • Feasibility: Parent satisfaction(10 weeks after parent baseline)

Study Sites (1)

Loading locations...

Similar Trials