Piaget-Based Nutrition Education in Preschools (PNEP)

August 23, 2026 updated by: Perihan Solmaz, Uşak University

Piaget-Based Nutrition Education in Preschools: An Explanatory Sequential Mixed-Methods Evaluation

This explanatory sequential mixed-methods study evaluated a six-week Piaget-based nutrition education programme for preschool children. Seven public preschools were randomized at the school level to an intervention condition (three preschools) or a usual-curriculum control condition (four preschools). The intervention consisted of six weekly, approximately 30-minute, developmentally tailored sessions delivered to groups of children in their usual classrooms. Mothers completed measures of children's food consumption frequency, nutrition behavior, and eating behavior before and immediately after the programme. Following the quantitative phase, three focus groups with 18 mothers from intervention preschools explored perceived changes and helped interpret the quantitative patterns. Because preschool identifiers were not retained in the final analytical dataset, the reported child-level analyses did not adjust for clustering and are interpreted as exploratory.

Study Overview

Study Type

Interventional

Enrollment (Actual)

268

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

      • Uşak, Turkey (Türkiye), 64200
        • Preschools affiliated with the Provincial Directorate of National Education, Uşak

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

Yes

Description

The sample of the study consists of preschool children and their mothers.

Inclusion criteria for the sample:

  • Mothers of children aged 3-6 attending kindergartens affiliated with the Provincial Directorate of National Education
  • Mothers whose children do not have any health problems affecting their nutritional status
  • Mothers aged 18 and above
  • Mothers who are at least literate.

The exclusion criteria for the study are as follows:

  • Children with hearing and speech problems,
  • Children who do not understand or speak Turkish,
  • Children with any illness or learning difficulties,
  • Those who participate for a maximum of 2 weeks during the six-week nutrition training.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Piaget-Based Nutrition Education
Children attending the three intervention preschools received the six-week Piaget-based nutrition education programme in their usual classrooms. A total of 138 mother-child dyads were allocated to intervention preschools; 130 children received at least part of the programme, and 127 dyads were included in the reported per-protocol analysis.
The researcher delivered six weekly sessions, each lasting approximately 30 minutes, to groups of 8-15 preschool children in their usual classrooms. The programme was tailored to the preoperational stage of cognitive development and used simple language, concrete classification, play, pictures, coloring, cartoons, songs, sensory exploration, and fruit-yogurt preparation. Sessions addressed food groups; fruits; vegetables; energy- and growth-supporting foods; milk and dental health; and foods to be consumed every day or occasionally.
No Intervention: Usual Preschool Curriculum
Children attending the four control preschools continued their usual preschool curriculum and did not receive the Piaget-based nutrition education programme during the study period. A total of 130 mother-child dyads were allocated to control preschools, and 111 dyads were included in the reported analysis.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in food consumption frequency
Time Frame: Baseline and immediately after completion of the six-week intervention
In the Food Consumption Frequency Questionnaire, there are foods that include 7 food groups (dairy group, meat group, vegetable group, fruit group, grain group, oil/margarine group, and sweet group) aimed at determining the child's food consumption status (Güneş et al., 2016). Food consumption frequency is recorded in nine different categories (>6/day, 4-5/day, 2-3/day, 1/day, 5-6/week, 2-4/week, 1/week, 1-3/month, 1-none/month). The Food Consumption Frequency Questionnaire specific to Turkish children was developed by Güneş and colleagues in 2016. The form includes not only food items but also commonly used ingredients in Turkish cuisine. During the development phase of the form, a food atlas containing the most frequently consumed foods, beverages, and some Turkish dishes was used. Results are reported by food item or food group; the questionnaire does not yield a single total score.
Baseline and immediately after completion of the six-week intervention
Change in Nutrition Behavior Scale (NBS) Score
Time Frame: Baseline and immediately after completion of the six-week intervention
In determining eating behaviors, the Nutrition Behavior Scale developed by Edmundson et al. (1996) and adapted for Turkish children by Öztürk (2010) was used. The scale consists of fourteen different items, each containing two different food items-low-fat, high-fat, salty, and unsalted-depicted in pictures and presented as choices, to determine children's food consumption. Students are asked to indicate which of the two comparable food items in each question item they eat more. The scale items receive a value of -1 for unhealthy food and +1 for healthy food. The total score ranges from -14 to +14. A high total score on the scale indicates a healthy eating habit. The reliability of the scale has been reported as r=0.76 (Öztürk, 2010).
Baseline and immediately after completion of the six-week intervention
Change in Children's Eating Behavior Questionnaire (CEBQ) Subscale Scores
Time Frame: Baseline and immediately after completion of the six-week intervention
Developed by Wardle et al. (2001), the Children's Eating Behaviour Questionnaire (CEBQ) is a 35-item parent-reported instrument that assesses children's eating behaviours on a five-point Likert scale ranging from 1 (never) to 5 (always). It comprises eight subscales: Food Responsiveness, Emotional Overeating, Enjoyment of Food, Desire to Drink, Satiety Responsiveness, Slowness in Eating, Emotional Undereating, and Food Fussiness. Each subscale is scored separately, with higher scores indicating a greater level of the behaviour represented by that subscale. The original instrument demonstrated an eight-factor structure, with Cronbach's alpha coefficients ranging from 0.74 to 0.91. The Turkish validity and reliability study was conducted by Yılmaz et al. (2011).
Baseline and immediately after completion of the six-week 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)

September 30, 2022

Primary Completion (Actual)

February 20, 2023

Study Completion (Actual)

June 30, 2023

Study Registration Dates

First Submitted

July 7, 2026

First Submitted That Met QC Criteria

July 7, 2026

First Posted (Actual)

July 13, 2026

Study Record Updates

Last Update Posted (Actual)

August 25, 2026

Last Update Submitted That Met QC Criteria

August 23, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PAU-BESEG-2026-01

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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