- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07540234
Storybook-Based Nutrition Education for Preschoolers
Nutrition Education for Preschool Children: The Effect of Designing an Educator Storybook on Nutrition Behaviors
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey (Türkiye), 34349
- Bahcesehir University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
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
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:
|
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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:
|
Baseline (before intervention) and immediately after the storybook intervention ends (5 days of intervention)
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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).
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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.
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At the baseline (before intervention) of the study.
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Weight Measurement
Time Frame: At the baseline (before intervention) of the study.
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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.
|
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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.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Nutrition Disorders
- Overnutrition
- Body Weight
- Overweight
- Obesity
- Pathological Conditions, Signs and Symptoms
- Behavior
- Nutritional and Metabolic Diseases
- Signs and Symptoms
- Feeding Behavior
- Pediatric Obesity
- Food Fussiness
- Health Care Quality, Access, and Evaluation
- Investigative Techniques
- Epidemiologic Methods
- Data Collection
- Health Care Evaluation Mechanisms
- Quality of Health Care
- Public Health
- Environment and Public Health
- Psychotherapy
- Behavioral Disciplines and Activities
- Epidemiologic Measurements
- Nutrition Assessment
- Behavior Therapy
Other Study ID Numbers
- E-85646034-604.01-107411
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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