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RecruitingNCT07734545Updated Jul 29, 2026

Examining the Impact of the Parenting Young Children Check-up

An Early Phase 1 interventional study of The Parenting Young Children Check-up in Behavioral Health, Disruptive Behaviors and Parenting Behavior, sponsored by Wayne State University. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-29.

Sponsored by Wayne State University · Early Phase 1, Interventional, and Treatment

Phase
Early Phase 1
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The proposed project aims to evaluate the Parenting Young Children Check-up (PYCC) through a randomized clinical trial in a family medicine clinic in Detroit that primarily serves low-income families. Forty parents will be randomized to intervention (n = 20) or control (n = 20) conditions. We will follow up with parents 1 month and 3-months later to test the impact of the program on children's behavioral health/disruptive behavior problems, parenting, and parenting stress and to examine how much parents in the intervention group make use of and report satisfaction with the PYCC program.

Read the detailed description

This study will test three hypotheses. First, we hypothesize that randomization to the PYCC intervention group, as compared to the control group, will be related to reduced child behavioral health challenges and disruptive behavior problems. Second, we hypothesize that randomization to the PYCC intervention group, as compared to control, will be related to improved positive parenting and reduced parenting stress. Third, for parents in the intervention group, we hypothesize there will be high rates of module use on the PYCC website (i.e., >50%). Finally, for parents in the intervention group, we also hypothesize that there will be high rates of satisfaction with the PYCC overall and with each PYCC module.

02

Conditions studied

  • Behavioral Health
  • Disruptive Behaviors
  • Parenting Behavior
  • Parenting Stress

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03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Parent of child ages 2-5 years old
  • Report a score of 9 or higher on the Preschool Pediatric Symptoms Checklist

Exclusion criteria

Exclusion Criteria:

  • Does not speak/read English
  • Does not have access to a Smartphone
04

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Intervention

    This arm will go through the initial check-up of the Parenting Young Children Check-up (PYCC), receive text messages from the PYCC, and have access to modules on the PYCC website.

    Behavioral: The Parenting Young Children Check-up

  • No intervention
    No Intervention: Control

    This arm will only complete assessment measures.

Interventions

  • BehavioralThe Parenting Young Children Check-up

    The Parenting Young Children Check-up (PYCC) is a technology-based program for parents of young children with challenging behavior. The PYCC has three components: 1) the initial check-up, 2) text messages, and 3) the parenting program website.

05

What researchers measure

Primary outcomes

  1. Disruptive Behavior Problems

    Measured with the Eyberg Child Behavior Inventory

    Time frame: From enrollment (baseline) to follow-up at 1-month and 3-months post baseline

  2. Children's Behavioral Health Challenges

    Measured with the Preschool Pediatric Symptoms Checklist

    Time frame: From enrollment (baseline) to follow-up at 1-month and 3-months post baseline

Secondary outcomes

  1. Parenting Stress

    Measured with the Parenting Stress Index

    Time frame: From enrollment (baseline) to follow-up at 1-month and 3-months post baseline

  2. Parenting

    Measured with the Preschool Version of the Alabama Parenting Questionnaire

    Time frame: From enrollment (baseline) to follow-up at 1-month and 3-months post baseline

Other outcomes

  1. Use of Modules on the PYCC Website

    Number of modules used

    Time frame: From enrollment (baseline) to follow-up at 1-month and 3-months post baseline

  2. Satisfaction with the Parenting Young Children Check-up

    Time frame: From enrollment (baseline) to follow-up at 3-months post baseline

06

Study locations

1 of 1 sites recruiting
  • Henry Ford Health
    Detroit, Michigan 48202, United States
    Recruiting
07

References and documents

Study documents

  • Study protocol · Apr 6, 2026
  • Informed consent form · Sep 24, 2025

Documents are hosted by the registry — open the source record to download them.

08

Registry details

Key details

Study ID
NCT07734545
Lead sponsor
Wayne State University
Collaborators
Henry Ford Health System
Responsible party
Lucy (Kathleen) McGoron, Ph.D. (Assistant Professor, Wayne State University) — Principal investigator
First posted
Jul 29, 2026
Start date
Nov 6, 2025
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Jul 29, 2026

Study contacts

Lucy McGoron, Ph.D.
Contact
Lucy.K.McGoron@wayne.edu
13138064414

Oversight

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

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