The Parenting Young Children Check-up Evaluation

November 3, 2021 updated by: Lucy (Kathleen) McGoron, Ph.D., Wayne State University

Pediatric Motivational mHealth Parent Training for Child Disruptive Behaviors: Pilot Randomized Clinical Trial

The PYCC is a system for parents of young children (2-5 years old) with Disruptive Behavior Problems (DBPs). The program is designed with the intentions of being used a pediatric primary care visit. Parents that report elevated child behavior problems go through a three part program. First, they go through a brief intervention on a tablet (i.e., the initial check-up) to receive feedback and learn about the PYCC; the aim is to build motivation to make parenting changes and engage in the parenting young children check-up. Next, parents receive text messages to connect them to further parent training content. Finally, parent training content is delivered via a web-based resource (i.e., the PYCC website), which includes videos to teach parenting skills. In this pilot RCT, the investigators will focus on examining the impact of the brief intervention (i.e., the initial check-up). Secondarily, the investigators will examine overall impact of the whole PYCC program and use of the parenting training website.

Parents will learn about the research opportunity through select community-based organizations in Detroit, Michigan, local posting, and a local participant registry. Through a phone call, parents will complete a demographics questionnaire and the DBP screener. The investigators aim to screen 200 parents in order to enroll 40 parents in the clinical trial.

If parents report elevated DBPs and do not meet any exclusion criteria, then they will be eligible to further participate. Parents that are eligible will complete a consent form (i.e., an online information sheet) and then be randomly assigned to intervention (n = 20) or control (n = 20). Both groups will complete a brief baseline. Both groups will also learn about the Parenting Young Children Check-up (PYCC). However, the way in which they learn about the program will differ. The control group will see a brief description about the program (i.e., an online flier) and will receive a brochure for the program through the mail. The intervention group will go through the full PYCC initial check-up and also receive a brochure through the mail. Both groups will receive text messages prompting them to engage in the PYCC.

After initial participation, parents will be free to use, or not use, the Parenting Young Children Check-up web-based resource as much as they want. Parents will enter their phone number and first name when accessing the web-based content in order for use to track their engagement. All use of the web-based resource will start with "Session 1. In this, they will choose what parenting skills they want to learn. If parents go through session 1, they will be further connected to PYCC content through tailored text messages. Texts contain links to all PYCC web-based content. Parents will be able to learn content related to "Special Time," "Labeled Praise," "Family Rules," "Effective Commands," "Offering Choices," "Routines," "Removing Attention," "Logical Consequences," and "Time out." All content of the PYCC is based on evidence-based parent training program content.

The purpose of this project is evaluate the Parenting Young Children Check-up. In particular, the investigators are interested in if the initial check-up leads parents to engage in the PYCC (i.e., completing session 1 and using the parent training content on the PYCC website).

Hypotheses include:

Primary Hypothesis: The intervention group (i.e. those randomized to complete the full initial check-up) will visit the parent training website more than the control group. The investigators hypothesize that, compared to the control group, more parents in the control group with complete "session 1," and use the PYCC web-based content to learn parenting skills (i.e., more parents will use any of this content and parents will use it more frequently).

Secondary Hypothesis (a): Participants assigned to the intervention group, as compared to those in the control group, will have higher scores for all domains consistent with the Theory of Planned Behavior at follow-up.

Secondary Hypothesis (b). Participants in the intervention group will report high levels of satisfaction (i.e., >=4 on a 5-point scale).

The investigators will also explore the impact of the PYCC on reported parenting and child behavior problems. Furthermore, the investigators will explore the impact of the initial check-up on intentions to use the parent training website.

Study Overview

Study Type

Interventional

Enrollment (Actual)

38

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Michigan
      • Detroit, Michigan, United States, 48236
        • Merrill Palmer Skillman Institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age 18 or above
  • English speaking
  • Parent to a child ages 2-5
  • Report their child has elevated disruptive behavior problems on the Eyberg Child Behavior Inventory
  • Have Smartphone and CIAS program works on their phone

Exclusion Criteria:

  • Parent report that their child has an Autism Spectrum Disorder diagnosis
  • Parent report that their child has an intellectual disability
  • Parent report that their child is receiving treatment of Oppositional Defiant Disorder or ADHD

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
Parents assigned to the intervention condition will go through the Initial Check-up, which is a brief intervention that uses motivational content to promote use of the Parenting Young Children Check-up parenting education website. They will also receive text messages and a brochure to connect them to the parenting education website.
Parents assigned to the control condition will not go through the Parenting Young Children Check-up Initial Check-up. They will only go through assessment and then see a brief flier about the Parenting Young Children. Like the intervention condition, they will also receive text messages and a brochure to connect them to the Parenting Young Children Check-up parenting education website.
No Intervention: Assessment Only

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Initial use of the parenting training website session 1
Time Frame: 1 month
After learning about the program, the first point of program use is session 1 (i.e., selecting parenting skill to learn first); the investigators will track if parents completed session 1 (1) or did not (0)
1 month
Use of parent training content on the PYCC website (binary; yes or no)
Time Frame: 1 month
The investigators will measure if parents use the parent training content on the Parenting Young Children Check-up Website (binary; yes or no)
1 month
Number of uses of parent training content on the PYCC website
Time Frame: 1 month
The investigators will track how many of the parent training content modules parents use; there are 9 different areas of training content with two modules each, thus there is a possible range of 0-18
1 month
Use of parent training content on the PYCC website (binary; yes or no)
Time Frame: 3 months
The investigators will measure if parents use the parent training content on the Parenting Young
3 months
Number of uses of parent training content on the PYCC website
Time Frame: 3 months
The investigators will track how many of the parent training content modules parents use; there are 9 different areas of training content with two modules each, thus there is a possible range of 0-18
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Attitudes, norms, and perceived behavioral control; consistent with the Theory of Planned Behavior
Time Frame: Baseline; 1 month
Nine items total with 3 items each taping into each of the three elements of TPB (perceived norms, attitude, behavioral control); Rated on a 5 point scale (0 = Strongly Disagree, 1 = Disagree, 2 = neither disagree nor agree, 3 = Agree, 4 =Strongly Agree)
Baseline; 1 month
Change in Attitudes, norms, and perceived behavioral control; consistent with the Theory of Planned Behavior
Time Frame: Baseline; 3 months
Nine items total with 3 items each taping into each of the three elements of TPB (perceived norms, attitude, behavioral control); Rated on a 5 point scale (0 = Strongly Disagree, 1 = Disagree, 2 = neither disagree nor agree, 3 = Agree, 4 =Strongly Agree)
Baseline; 3 months
Technology Acceptance with initial check-up
Time Frame: Baseline;
6 Items specific to the initial check-up derived from the technology acceptance model tapping including ease of use, usefulness, and satisfaction, 5-point scale (0 = Strongly Disagree, 1 = Disagree, 2 = neither disagree nor agree, 3 = Agree, 4 =Strongly Agree)
Baseline;
Technology Acceptance Parenting Young Children Check-up
Time Frame: 1 month
18 Items focused on all the elements the PYCC program that are derived from the 1technology acceptance model and tap into ease of use, usefulness, and satisfaction; 5-point scale (0 = Strongly Disagree, 1 = Disagree, 2 = neither disagree nor agree, 3 = Agree, 4 =Strongly Agree)
1 month

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Child Disruptive Behavior Intensity
Time Frame: Baseline; 1 month; 3 month
Eyberg child behavior inventory; 36 items rated on a 7 point scale ((Never=1; Seldom=2-3; Sometimes=4; Often=5-6; Always=7))
Baseline; 1 month; 3 month
Change in Child Disruptive Behavior Intensity
Time Frame: Baseline; 3 month
Eyberg child behavior inventory; 36 items rated on a 7 point scale ((Never=1; Seldom=2-3; Sometimes=4; Often=5-6; Always=7))
Baseline; 3 month
Change in Child Disruptive Behavior Problems Count
Time Frame: Baseline; 1 month
Eyberg child behavior inventory; 36 items rated as a problem or not (0 =no, 1 = yes)
Baseline; 1 month
Change in Child Disruptive Behavior Problems Count
Time Frame: Baseline; 3 months
Eyberg child behavior inventory; 36 items rated as a problem or not (0 =no, 1 = yes)
Baseline; 3 months
Change in Parenting
Time Frame: Baseline; 1 months
The Alabama Parenting Questionnaire; 31 items rated on a 5-point scale (1 = never, 5 = always)
Baseline; 1 months
Change in Parenting
Time Frame: Baseline; 3 months
The Alabama Parenting Questionnaire
Baseline; 3 months
Intentions to use the PYCC parent training website
Time Frame: Baseline
1 items taping into parents intentions to use the PYCC parent training website
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 29, 2020

Primary Completion (Actual)

October 31, 2021

Study Completion (Actual)

October 31, 2021

Study Registration Dates

First Submitted

September 28, 2020

First Submitted That Met QC Criteria

November 12, 2020

First Posted (Actual)

November 13, 2020

Study Record Updates

Last Update Posted (Actual)

November 4, 2021

Last Update Submitted That Met QC Criteria

November 3, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • K01MH110600B
  • K01MH110600 (U.S. NIH Grant/Contract)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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