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Clinical Trials in the USA / NCT07417930
Recruiting Not applicable

Hybrid Delivery to Increase Access and Sustainability: Evaluating ezParent Implementation

NCT07417930 · tracked via the Priya Life Science USA tracker
Sponsor
Klein Buendel, Inc.
Phase
Not applicable
Started
2026-07-27
Last updated
2026-08-03

Condition(s) studied

ParentingPreventionProgram ImplementationEarly Childhood

Investigational drug(s) / intervention(s)

ezParent

ezParent: Hybrid ezParent includes the web-based ezParent program and 4 synchronous group sessions. ezParent is a 6-module digital delivery of the group-based Chicago Parent Program (CPP). The purpose of the program is to strengthen parenting, decrease child behavior problems, and increase child prosocial behavior. Each module includes: a video narrator describing parenting strategies; video vignettes of parents and children as examples of how parenting strategies work; questions following each vignette for parents to reflect upon; interactive activities for parents to complete; knowledge questions to assess parent understanding of the strategies; and practice assignments. Parents are instructed to complete modules independently between synchronous group sessions. Group sessions are 1-1.5 hours and follow a discussion guide to reinforce key content, build community, and support parents in using ezParent. Trained facilitators lead groups of about 10 parents either in-person or virtual.

Study summary

The goal of this study is to evaluate the effects of the hybrid ezParent program (e.g., web-based training program plus synchronous group sessions) on parent and child outcomes in a community setting serving parents of children 2-5 years old. Parent participants will complete surveys at baseline, and 10 and 24-weeks post baseline.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
Accepted
Inclusion Criteria: * Parent or legal guardian of a 2-5-year-old child receiving services at the partnering organization site. * Speaks English or Spanish. * Has a smartphone, tablet, or computer with Wi-Fi access to receive the ezParent program. Exclusion Criteria: • Parents who have previously participated in CPP or ezParent will be excluded.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Ohio State University Columbus Ohio Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07417930 on ClinicalTrials.gov ↗ ← All trials in the USA