Cognitive-Based Behavior Change Training Program

May 14, 2025 updated by: SELMA HASANOĞLU, Uskudar University

The Effect of the 'Cognitive-Based Behavior Change Training Program' Applied to Parents of Preschool Children With Behavior Problems on Parents' Attitudes and Stress Levels Towards the Child and on the Problematic Behaviors of the Children

This study will be conducted to determine the effects of the Parent Education Program Based on the Cognitive Development of the Child, which is applied to the parents of preschool children with behavioral problems, on the attitudes and stress levels of the parents and the problematic behaviors of the children.

The purpose of this study has two dimensions;

Dimension 1: The 'Parent Education Program Based on the Cognitive Development of the Child', which is planned to be developed for the purpose of measuring the attitudes, stress levels of the parents and the effects on the problematic behaviors of the children.

The development of the program was based on Jean Piaget's theory of cognitive development.

Dimension: It is experimental. The aim is to reveal the effectiveness of the Parent Education Program, which will be applied to the parents of children with behavioral problems. There are parent training programs developed for children with behavioral problems in the preschool period. However, the lack of parent studies based on the child's cognitive development reveals the rationale and importance of this study.

Study Overview

Study Type

Interventional

Enrollment (Actual)

44

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

      • Gazi̇antep, Turkey
        • Gaziantep Municipality Kindergartens

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

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Children must be between the ages of 3-6
  • Participating in the study as a mother and father together
  • Not having attended any parent training

Exclusion Criteria:

  • Participating in the study as a single parent
  • The child must have been diagnosed in the special needs category

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental Group
Implementation of the 8-session parent study

Parents will be given an 8-session parent training program.

Session 1: Establishing a trusting relationship and informing them about the study Session 2: Informing parents about the cognitive development of 3-6 year old children Theme: Children learn with 'numbers/scales/amounts' Session 3: Parents being consistent in their approach to children Theme: Children learn with the all/or nothing rule Session 4: Reinforcing positive behaviors in children Theme: Children Learn Laterally Session 5: Parents being positive models Theme: Children Learn by Imitation Session 6: Guidance of parents on the principle of 'learning by doing and experiencing' Theme: Children Learn by Action Session 7: This is the last session. Session 8: Application of final tests and saying goodbye.

No Intervention: Control groups
Group where parental work was not implemented

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Preschool Behavior Problems Screening Scale
Time Frame: One month prior to the intervention / One month following the intervention
The "Preschool Behavior Questionnaire" developed by Behar (1976; Cited in Kanlıkılıçer, 2005) is a Likert-type scale used to determine the behavioral problems of preschool children. The scale was adapted to Turkish by Kanlıkılıçer, and the propositions in the scale were converted into questions and used. The original Turkish version of the "Preschool Behavior Problems Screening Scale" consists of 30 items. After the factor analysis conducted for this study, items with item loading values below .50 were removed, so 15 items were used. The highest score a child can get from the "Preschool Behavior Problems Screening Scale" is "30", and the lowest score is "0".
One month prior to the intervention / One month following the intervention
Parent Stress Scale
Time Frame: One month prior to the intervention / One month following the intervention
The "Parenting Stress Scale" was developed to measure the stress experienced by parents of children with normal developmental characteristics regarding parenting. The scale consists of 18 items and has a single-dimensional structure that includes the parent, parent-child relationship, and the characteristics of the child. The Parenting Stress Scale is a Likert-type measurement tool evaluated from 0 (Does not describe at all) to 4 (Describes very well). The range of scores that can be obtained from the scale is between 0-72, with higher scores indicating the level of parenting stress. The scale is a measurement tool that can be easily applied to parents with at least one child with a primary school education level or higher.
One month prior to the intervention / One month following the intervention
Parent Attitude Scale
Time Frame: One month prior to the intervention / One month following the intervention

The Parental Attitude Scale was developed by Evren Karabulut Demir to measure the attitudes of parents with children aged 2 to 6 years, and its validity and reliability study was conducted in collaboration with Gül Erdil. The scale is designed to be applied to parents of children within this age range and consists of 46 items grouped under four subdimensions: Democratic, Authoritarian, Overprotective, and Permissive. The scale is structured in a 5-point Likert format, with each item offering five response options that vary based on frequency or degree of agreement. Participants are asked to indicate their level of agreement with each statement using the following options:

1 = Strongly disagree, 2 = Disagree, 3 = Neutral, 4 = Agree, and 5 = Strongly agree.

This Likert-type rating system allows for a quantitative evaluation of parental attitudes across the specified subdimensions. Some items are negatively worded and are therefore reverse-coded prior to analysis. Higher scores within ea

One month prior to the intervention / One month following the intervention

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)

April 1, 2025

Primary Completion (Estimated)

September 1, 2025

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

April 27, 2025

First Submitted That Met QC Criteria

May 14, 2025

First Posted (Actual)

May 22, 2025

Study Record Updates

Last Update Posted (Actual)

May 22, 2025

Last Update Submitted That Met QC Criteria

May 14, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • E-97105791-050.04-51964

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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