- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06392035
Breakfast Training Based on PENDER's Health Promotion Model (HPM) ((HPM))
Determining the Effect of Nutrition Education Based on PENDER's Health Promotion Model on the Breakfast Habits of Secondary School Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: SEÇİL DURAN YILMAZ
- Phone Number: 05465772813
- Email: secilduran.91@gmail.com
Study Locations
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Karaman, Turkey
- Seçil Duran Yilmaz
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Contact:
- Karaman İl Milli Eğitim Müdürlüğü
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Being a 7th grade student of secondary school,
- Not having a chronic disease
- Students who voluntarily agreed to participate in the research and received consent from their parents.
Exclusion Criteria:
• Not being a 7th grade student of secondary school,
- Having a chronic disease
- Students who do not agree to participate in the research voluntarily and whose parents' consent cannot be obtained
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control Group
No intervention will be made to the participants in the control group.
A pre-test will be administered before the study and a post-test will be administered after the study.
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Experimental: Intervention Group
Secondary schools located in Karaman city center will be visited. The researcher will introduce himself and explain the purpose of the research. A research inclusion form will be applied to those who agree to participate in the research. "Sociodemographic Data Form", "Nutrition Behavior Scale", "Parental Questionnaire" and "Tool for Measuring the Health Promotion Model Related to Breakfast Consumption" will be applied as pre-test forms to the participants who meet the inclusion criteria. Participants will be assigned randomization by someone other than the researcher. After randomization assignment, a 6-week web-based training based on PENDER's Health Promotion Model, prepared in line with the literature, will be applied. |
Data collection tools will be filled in by two study groups (experimental group, control group) and based on the pre-test results of both groups, Pender's SGM-based breakfast training will be given only to the experimental group.
No intervention will be made to the control group.
In this study, a total of 6 sessions will be held for the experimental group for 6 weeks (one session per week), each lasting 40 minutes.
In these sessions, web-based training will be given every week according to the components of the model and will be supported with written and visual brochures.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Teaching children the habit of regular breakfast
Time Frame: at the end of the 1th weeks
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Children will be taught regular breakfast habits.
Here, weight, height and BMI status will be examined.
Weight in kilograms; Height will be measured in metres.
Weight and height will be combined.
BMI will be reported in kg/m^2.
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at the end of the 1th weeks
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Teaching children the habit of regular breakfast
Time Frame: at the end of the 6th weeks
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Children will be taught regular breakfast habits.
Here, weight, height and BMI status will be examined.
Weight in kilograms; Height will be measured in metres.
Weight and height will be combined.
BMI will be reported in kg/m^2.
|
at the end of the 6th weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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"Health Promotion Model Related to Breakfast Consumption (first week) )
Time Frame: at the end of the 1th weeks
|
Health Promotion Model Related to Breakfast Consumption scale consists of 10 sub-dimensions and 58 items. Previous Relevant Behavior (first 10 questions - score range 10-50) Perceived Usefulness (questions 11-16 - score range 6-30) Perceived Obstacles (questions 17-24-score range 8-40) Perceived Self-Efficacy (questions 25-32 - score range 8-40) Positive Impact (33,34 questions - score range 2-10) Negative Impact (35,36 questions - score range 2-10) Interpersonal Influences (questions 37-46 - score range 10-50) Situational Effects (questions 47,48,49 - score range 3-15) Instant Competing Demands and Preferences (questions 50,51,52,53 - score range 4-20) Planning Commitment (questions 54-58 - score range 5-20) |
at the end of the 1th weeks
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Nutrition behavior scale (first week)
Time Frame: at the end of the 1th weeks
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Children's food consumption was evaluated with the "Nutrition Behavior Scale" developed within the scope of CATCH (Child and Adolescent Trial for Cardiovascular Health)HBQ (Health Behavior Questionnaire). The scale consists of 14 visual items with low-fat/salty and high-fat/salty food options to determine children's food consumption. Children are shown comparable foods and asked which of the two foods is more common (often). Trying to find out what he ate. Scale items take values of -1 for unhealthy food and +1 for healthy food. The lowest and highest scores that can be obtained from this scale are between -14 and +14. A high total score from the scale indicates that you have healthy eating habits. The internal consistency reliability coefficient of the original scale was found to be 0.76, and the test-retest reliability was 0.58 (Edmunson et al., 1996). Scale validity and reliability study for this scale was conducted by Öztürk (2010). |
at the end of the 1th weeks
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Parent Questionnaire
Time Frame: at the end of the 1th weeks
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The parent questionnaire contains 18 questions asked to parents about their children, created by the researcher by scanning the literature.
The questionnaire will be scored between 18-90.
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at the end of the 1th weeks
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: HAVVA KARADENİZ, Research Supervisör-hkmumcu@ktu.edu.tr
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- 13562490-299-55
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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