Storybook-Based Nutrition Education for Preschoolers

April 17, 2026 updated by: Ilayda Ozturk Altuncevahir, Bahçeşehir University

Nutrition Education for Preschool Children: The Effect of Designing an Educator Storybook on Nutrition Behaviors

This project aims to design a nutrition-based educational storybook for preschool children and to evaluate its effect on improving general nutrition behaviors and reducing possible picky eating habits.

Study Overview

Detailed Description

This study aims to develop a nutrition-focused educational storybook for preschool children (ages 5-6) and assess its impact on improving eating behaviors and reducing picky eating. Picky eating is common in early childhood and can negatively affect nutrition and growth, potentially leading to health issues later in life. The study will use a crossover design with 60 healthy children from kindergartens in Istanbul. Participants will experience both the intervention (storybook) and control conditions. Parental consent will be obtained, and data confidentiality will be maintained.

Study Type

Interventional

Enrollment (Actual)

70

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

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

Inclusion Criteria:

  • Children aged 5-6 years and free from any diagnosed chronic health conditions.

Exclusion Criteria:

  • Children younger than 5 years or older than 6 years, and those diagnosed with any chronic health conditions.

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: Screening
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Intervention group
Healthy preschool age children

In the first week, children in the intervention group were exposed to a structured, story-based nutrition education program. On the first day, the teacher read the designed storybook to the children for approximately 12-15 minutes. Children in the control group continued their routine classroom activities without exposure to nutrition-related content.

During the remaining four days of the week, reinforcement activities were implemented to support the main message of the story, which emphasized the importance of fruit and vegetable consumption and healthy eating. These activities were developed in consultation with a child development specialist and were based on active learning and repetition principles.

The reinforcement activities included age-appropriate tasks such as coloring, cutting, pasting, and drawing. Specifically, children participated in activities involving coloring story-related characters, selecting and pasting healthy food items onto visual materials, drawing their fa

Other Names:
  • nutrition education
No Intervention: Control group
Healthy preschool age children

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Choice of Snack (Healthy vs. Unhealthy) Measured by Direct Observation
Time Frame: Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention).

At the baseline and right after the storybook intervention ends, each child will be offered a snack choice: fruit/vegetables (healthy) or cookies (unhealthy). The selection will be recorded using a standardized observation form. The primary outcome will be analyzed as the number and percentage of children selecting the healthy snack.

Unit of Measure: Number and Percentage of Children Choosing a Healthy Snack

Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
NutriSTEP Questionnaire (OBTA Questionnare)
Time Frame: Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention)

Turkish version of NutriSTEP Questionnaire (OBTA Questionnare) will be used to detect children's nutritional status. The scale will be filled by the parents of the children. It is fast and simple to use to scan eating habits and identify nutritional problems. It is a form that can identify preschool children who are and are not in risky nutritional status.Each question has 2-5 response options, with each option scored from 0 (no risk) to 4 (high risk). The total score is calculated by summing the scores obtained from all questions. Higher total scores indicate greater risk in dietary behavior. The total score can range from 0 to 68. According to the OBTA cut-off points:

≤20 points = low risk 21-25 points = moderate risk

≥26 points = high risk OBTA four

It contains 17 questions in the category:

  • Food and liquid intake
  • Physical growth and development
  • Physical activity and sedentary behavior
  • Factors affecting food intake and nutritional behavior
Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention)
Nine-Item Avoidant/Restrictive Food Intake Disorder Screen (NIAS) Parent-Report
Time Frame: Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention)
In order to evaluate their nutritional behaviors and detect potential disrupted eating habits, the "Avoidant/Restrictive Food Intake Disorder (ARFID) Parent Questionnaire", which is a 9-item scale that has been validated in Turkish (as ARFID scale) and applied to the parents of individuals between the ages of 2-18, will be filled out by the mothers of the participants. There NIAS has three subscales. The maximum score is 15 for the subscales and the total maximum score is 45 points. As the score increases the risk of ARFID increases too.
Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention)
Visual Scales
Time Frame: Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention)
Various questions will be asked to assess the children's cognitive, automatic, and detailed emotional responses. To measure children's cognitive, automatic and detailed emotional reactions, various questions will be asked and their reactions will be observed using a 4-point visual scale. For example, when measuring cognitive response, "How strong does eating fruit/vegetables make you?" and children's answers will be evaluated using a 4-point visual scale with squares from smallest to largest. Automatic emotional response to children quickly determine whether they like fruits/vegetables or not. Children's immediate liking of fruits/vegetables will be assessed using a two-choice facial expression scale (happy vs. sad). Detailed emotional response will be measured with two questions ("How much do you like fruits/vegetables?" and "How do you like the taste of fruit/vegetables?") using a 4-point facial expression scale (1 = not at all, 4 = like a lot).
Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Height measurement
Time Frame: At the baseline (before intervention) of the study.
Children will be barefoot with their heads in the Frankfurt plane; heels, hips, back, and head aligned as upright as possible; knees straight; and standing comfortably. The headpiece will be gently placed at a right angle. Measurements will be recorded to the nearest millimeter and repeated twice, with the average taken.
At the baseline (before intervention) of the study.
Weight Measurement
Time Frame: At the baseline (before intervention) of the study.
Weight will be measured using a digital scale: children will wear light clothing and be barefoot; the scale will be placed on a flat, calibrated surface. Children will stand balanced, not move, and distribute weight evenly. Each measurement will be performed twice and averaged. Weight will be recorded in kilograms with 0.1 kg precision.
At the baseline (before intervention) of the study.
Body Mass Index Calculation and BMI z-scores
Time Frame: At the baseline (before intervention) of the study.

Body Mass Index (BMI) and BMI z-scores BMI will be calculated as weight (kg) divided by height squared (m²), and BMI z-scores will be determined according to WHO standards.

Unit of Measure: kg/m² (for BMI) and z-score (unitless) [Time Frame: At the baseline (before intervention) of the study.]

At the baseline (before intervention) of the study.

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)

November 1, 2025

Primary Completion (Actual)

January 21, 2026

Study Completion (Actual)

January 21, 2026

Study Registration Dates

First Submitted

July 31, 2025

First Submitted That Met QC Criteria

April 17, 2026

First Posted (Actual)

April 20, 2026

Study Record Updates

Last Update Posted (Actual)

April 20, 2026

Last Update Submitted That Met QC Criteria

April 17, 2026

Last Verified

April 1, 2026

More Information

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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