Hybrid Delivery to Increase Access and Sustainability: Evaluating ezParent Implementation
ezParent FT
2 other identifiers
interventional
516
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 10, 2026
CompletedFirst Posted
Study publicly available on registry
February 18, 2026
CompletedStudy Start
First participant enrolled
August 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2028
Study Completion
Last participant's last visit for all outcomes
September 30, 2028
February 27, 2026
February 1, 2026
2.2 years
February 10, 2026
February 24, 2026
Conditions
Outcome Measures
Primary Outcomes (4)
Multidimensional Assessment of Parenting Scale (MAPS) Parent-form - Version 2.0
A 35-item scale measures parenting practices constituting both positive and negative dimensions of warmth/hostility and behavioral control appropriate for parents of children across the developmental span from young childhood through adolescence. Parents respond to each item on a 5-point scale from "Never" to "Always". Possible range= 0-175
Baseline, 10- and 24-weeks post-baseline
Child-Parent Relationship Scale-Short Form (CPRS-SF)
The CPRS-SF has 15 items that parents rate their perception of their relationship with their child. The measure taps into positive and negative aspects of parent-child relationships. The CPRS-SF is rated on a 5-point scale with two subscales of closeness and conflict. Possible range= 0-35
Baseline, 10- and 24-weeks post-baseline
Parenting Sense of Competence Scale (PSOC)
The Parenting Sense of Competence Scale (PSOC) has 17 items, with 2 subscales: satisfaction (person's liking of the parenting role) and efficacy (person's perceived competence in the parenting role). Scale: 6-point Likert scale (1 = strongly disagree, 6 = strongly agree) Minimum item score = 1 Maximum item score = 6 Subscale scoring (satisfaction and efficacy): Higher scores means a better outcome
Baseline, 10- and 24-weeks post-baseline
Strengths and Difficulties Questionnaire (SDQ)
The Strengths and Difficulties Questionnaire (SDQ) is 25-items with five subscales: emotional symptoms, conduct problems, hyperactivity-inattention, peer problems, and prosocial behavior. A total difficulties score (TDS) is generated from the emotional, conduct, hyperactivity- inattention, and peer problems scales. Scale: 3-point scale (not true, somewhat true, and certainly true). Minimum item score = 0 Maximum item score = 2 Minimum subscale score = 0 Maximum subscale score = 10 Subscale scoring - Prosocial subscale: Higher score means a better outcome All other subscales (emotional, conduct, hyperactivity, peer): Higher scores means a worse outcome
Baseline, 10- and 24-weeks post-baseline
Study Arms (2)
Hybrid ezParent Intervention
EXPERIMENTALHybrid 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.
Control
NO INTERVENTIONParticipants receive usual services for parents and families at their agency during the study period.
Interventions
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.
Eligibility Criteria
You may qualify if:
- Parent or legal guardian of a 2-5-year-old child receiving services at the partnering organization site.
- Speaks English.
- Has a smartphone, tablet, or computer with Wi-Fi access to receive the ezParent program.
You may not qualify if:
- Parents who have previously participated in CPP or ezParent will be excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Johns Hopkins Universitycollaborator
- Klein Buendel, Inc.lead
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)collaborator
- Ohio State Universitycollaborator
Study Sites (1)
The Ohio State University
Columbus, Ohio, 43210, United States
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 10, 2026
First Posted
February 18, 2026
Study Start (Estimated)
August 1, 2026
Primary Completion (Estimated)
September 30, 2028
Study Completion (Estimated)
September 30, 2028
Last Updated
February 27, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- Deidentified data for the shared database will be made available after the main findings from the final dataset have been accepted for publication.
- Access Criteria
- The data that is shared will be openly accessible via LDbase.