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Pediatric ObesityNCT07540234

Storybook-Based Nutrition Education for Preschoolers

A study testing Behavioral Treatment in people with Pediatric Obesity and Pediatric Nutrition, run by Bahçeşehir University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 5 to 6 yearsHealthy volunteers can take part
What is being tested?
Behavioral Treatment
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Nov 2025to 21 Jan 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 5 to 6 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Bahcesehir University

    Istanbul, 34349

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Read the 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.

Being tested
Behavioral Treatment
Keywords
preschool nutrition, picky eating, eating behaviour intervention, child nutrition education, educational storybook
Medical subject headings
Pediatric Obesity, Food Fussiness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Behavioral TreatmentBehavioural

    Also called nutrition education

    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

Study groups in NCT07540234
Study groupRoleWhat they receive
Intervention groupOtherHealthy preschool age children
Receives: Behavioral: Behavioral Treatment
Control groupNo interventionHealthy preschool age children

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Choice of Snack (Healthy vs. Unhealthy) Measured by Direct Observation

    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

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

Secondary outcomes (3)
  1. NutriSTEP Questionnaire (OBTA Questionnare)

    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

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

  2. Nine-Item Avoidant/Restrictive Food Intake Disorder Screen (NIAS) Parent-Report

    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.

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

  3. Visual Scales

    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).

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Apr 2026
  2. Study start1 Nov 2025
  3. Primary completion21 Jan 2026
  4. Study completion21 Jan 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Screening
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Participant
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07540234
Sponsor's protocol ID
E-85646034-604.01-107411
Status last verified
Apr 2026
First submitted
31 Jul 2025
Last updated
20 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Behavioral Treatment in people with Pediatric Obesity and Pediatric Nutrition, run by Bahçeşehir University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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).). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Apr 2026.

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