ClinicalTrials.gg
RecruitingNCT07750054Updated Aug 6, 2026

Testing the Impact of the Parenting Young Children Check-up

An Early Phase 1 interventional study of 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 2026-08-06.

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

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Nov 2025, registered Jul 2026).
  • Started Nov 2025; still recruiting 1 year later.
Phase
Early Phase 1
Study type
Interventional
Enrollment
50
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 pediatric primary care practice in Detroit that primarily serves low-income families. Fifty parents will be randomized to intervention (n = 25) or control (n = 25) 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

In context

Problem Behavior

178 studies on the registry are indexed under Problem Behavior; 47 are open to participants now.

This study's planned enrollment of 50 is below the median of 90 across 165 interventional studies indexed under Problem Behavior.

Browse Problem Behavior studies →

Lead sponsor

Wayne State University is the lead sponsor of 230 studies on the registry; 35 are open to participants now.

Of its 17 completed or terminated interventional studies of FDA-regulated products, 4 (24%) have results posted.

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
No

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 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
05

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 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: Parenting Young Children Check-up

  • No intervention
    Control

    This arm will only complete assessment measures.

Interventions

  • BehavioralParenting 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.

06

What researchers measure

Primary outcomes

  1. Disruptive Behavior Problems

    Measured with the Eyberg Behavior Checklist

    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

07

Study locations

1 of 1 sites recruiting
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No — All participation will be confidential.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Nov 2025 (actual). Primary completion is estimated for Dec 2026, 13 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 23, 2026
First posted
Aug 6, 2026
StartActual
Nov 1, 2025
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2026
Last update
Aug 6, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07750054
Responsible party
Lucy (Kathleen) McGoron, Ph.D. (Assistant Professor, Wayne State University) — Principal investigator
First posted
Aug 6, 2026
Start date
Nov 1, 2025
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Aug 6, 2026

Study contacts

Lucy McGoron
Contact
Lucy.K.McGoron@wayne.edu
313-664-2500

Oversight

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

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