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Completed

NCT Number: NCT07540234

Storybook-Based Nutrition Education for Preschoolers

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.

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Key information

Age range

5 year–6 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bahcesehir University

Istanbul, 34349, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Behavioral Treatment

Behavioral

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

Primary outcomes

  1. 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

Secondary outcomes

  1. 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
  2. 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.

  3. 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).

Other outcomes

  1. 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.

  2. 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.

  3. 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.]

Sponsors and collaborators

Lead sponsor

Bahçeşehir University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 20, 2026
Registry last updated
Apr 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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