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RecruitingNCT07417930ezParent FTUpdated Aug 3, 2026

Hybrid Delivery to Increase Access and Sustainability: Evaluating ezParent Implementation

An interventional study of ezParent in Parenting, Prevention and Program Implementation, sponsored by Klein Buendel, Inc.. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-03.

Sponsored by Klein Buendel, Inc. · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started Jul 2026; still recruiting 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
516
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

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.

Read the detailed description

Positive parenting practices (e.g., supportive, consistent, responsive) buffer the negative effects of early adverse experiences by developing safe, stable, and nurturing environments. Positive parenting practices are important in strengthening and creating positive childhood and supporting optimal child social and behavioral development. Parent training (PT) is the gold standard for supporting and strengthening parenting practices and preventing and treating child behavior problems. The PT program proposed in this study is the web-based adaptation of the evidence-based based Chicago Parent Program (CPP), called ezParent. The purpose of this study is to test the effects of hybrid delivery of ezParent versus a waitlist control on parent and child outcomes. Hybrid ezParent combines the self-administered ezParent with virtual or in-person group meetings. Hybrid ezParent lasts \~ 8 weeks and includes four 1-1.5 hour group sessions led by trained facilitators, held via Zoom or in person. Facilitators follow a discussion guide to reinforce content, build community, and support program use.

A cluster-randomized trial will be conducted with 16 organizations (sites) randomized to either the intervention (hybrid ezParent) or control condition (waitlist control). There will be 8 sites per condition. Each site will recruit approximately 32 parents of children aged 2-5 years, for a total sample size of approximately 516 parents. All participating parents within a given site will receive the condition assigned to that site. Once sites are randomized to intervention or waitlist control, parents are invited to participate through recruitment materials. Outcome data will be collected from parents at 3 timepoints over 6 months at baseline, and 10 and 24- weeks post-baseline. Outcome data includes parenting skills and self-efficacy, parent-child relationship, and reductions in child behavior problems.

02

Conditions studied

  • Parenting
  • Prevention
  • Program Implementation
  • Early Childhood
03

In context

Lead sponsor

Klein Buendel, Inc. is the lead sponsor of 35 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Parents who have previously participated in CPP or ezParent will be excluded.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
516 participants (estimated)

Study arms

  • Experimental
    Hybrid ezParent Intervention

    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.

    Behavioral: ezParent

  • No intervention
    Control

    Participants receive usual services for parents and families at their agency during the study period.

Interventions

  • BehavioralezParent

    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.

06

What researchers measure

Primary outcomes

  1. 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

    Time frame: Baseline, 10- and 24-weeks post-baseline

  2. 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

    Time frame: Baseline, 10- and 24-weeks post-baseline

  3. 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

    Time frame: Baseline, 10- and 24-weeks post-baseline

  4. 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

    Time frame: Baseline, 10- and 24-weeks post-baseline

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Statistical analysis plan

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.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07417930
Responsible party
Sponsor
First posted
Feb 18, 2026
Start date
Jul 27, 2026
Primary completion
Sep 30, 2028 (estimated)
Completion
Sep 30, 2028 (estimated)
Last update
Aug 3, 2026

Study contacts

Susan M Breitenstein, PhD
Contact
breitenstein.5@osu.edu
614-688-4614

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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