Effect of a Nutrition Education Intervention on Ultra-Processed Food Awareness and Consumption Among University Students
Tıp Fakültesi Öğrencilerinde "Besinini Bilinçli Tüket, Sağlığı Seç" Eğitim Programının Ultra İşlenmiş Gıda Farkındalığına Etkisinin Değerlendirilmesi: Yarı Deneysel Kontrollü Çalışma
1 other identifier
interventional
74
1 country
1
Brief Summary
Ultra-processed foods are industrially formulated products that often contain high amounts of salt, sugar, and saturated fat, as well as additives. Higher consumption of these foods has been associated with several chronic diseases. Medical students may be at increased risk of unhealthy dietary behaviors and food insecurity. This study aims to evaluate the effects of a low-cost nutrition education program on medical students' knowledge and attitudes about ultra-processed foods, ultra-processed food consumption, nutrition label literacy, and nutrition self-efficacy. A total of 74 sixth-year medical students at Eskisehir Osmangazi University Faculty of Medicine will be assigned by clusters to either an intervention group or a control group. The intervention group will participate in an educational program about ultra-processed foods, food labels, and healthier food choices. The control group will not receive this educational program during the study period. Data will be collected at baseline, immediately after the intervention, and at the one-month follow-up. The study will assess food security, knowledge and attitudes regarding ultra-processed foods, ultra-processed food consumption, nutrition label literacy, nutrition self-efficacy, and dietary intake based on three-day food records.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
CompletedFirst Submitted
Initial submission to the registry
August 6, 2026
CompletedFirst Posted
Study publicly available on registry
August 12, 2026
CompletedAugust 12, 2026
August 1, 2026
19 days
August 6, 2026
August 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in Ultra-Processed Food Consumption
Ultra-processed food consumption will be assessed using the Turkish version of the Short Screening Questionnaire for Highly Processed Food Consumption (sQ-HPF). The total score ranges from 0 to 11, with higher scores indicating higher consumption of ultra-processed foods. Scores of 6 or above indicate a high level of ultra-processed food consumption.
Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)
Change in Ultra-Processed Food Knowledge
Knowledge of ultra-processed foods will be assessed using a list of 20 foods, including 10 ultra-processed and 10 non-ultra-processed foods. Participants will classify each food according to whether it is ultra-processed. One point will be awarded for each correct classification. The total score ranges from 0 to 20, with higher scores indicating greater accuracy in identifying ultra-processed foods.
Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)
Secondary Outcomes (7)
Change in Food Processing Knowledge
Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)
Change in Nutrition Label Literacy
Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)
Change in Nutrition Self-Efficacy
Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)
Change in the Acceptability of Front-of-Pack Nutrition Labels
Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)
Change in Purchase Intention for Products With Front-of-Pack Nutrition Labels
Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)
- +2 more secondary outcomes
Study Arms (2)
Nutrition Education Intervention
EXPERIMENTALParticipants in this arm will receive a structured nutrition education program focusing on ultra-processed foods, nutrition label literacy, food insecurity, nutrition self-efficacy, and healthier food choices. Measurements will be conducted before the intervention, immediately after the intervention, and at the one-month follow-up.
Control Group
NO INTERVENTIONParticipants in this arm will not receive the structured nutrition education program during the study period. Measurements will be conducted at baseline, immediately after the intervention period, and at the one-month follow-up
Interventions
The multi-session nutrition education program is planned and implemented based on the PRECEDE-PROCEED Model. During the PRECEDE phase, problems related to ultra-processed food consumption and food insecurity among medical students are analyzed, and predisposing, enabling, and reinforcing factors are identified. The intervention content is structured to address these determinants. During the PROCEED phase, the education program is implemented, and its effects on participants' knowledge, attitudes, and behaviors are evaluated. The intervention is also informed by the Health Belief Model and Social Cognitive Theory. The program covers ultra-processed foods, the NOVA food classification system, associations between ultra-processed food consumption and chronic diseases, nutrition label reading, front-of-pack nutrition labels, food insecurity, nutrition self-efficacy, and healthier food choices. It includes presentations, small-group discussions, interactive quizzes, case-based learning, rol
Eligibility Criteria
You may qualify if:
- Agreeing to participate in the study
- Being a medical faculty student
- Being able to understand Turkish
- Being 18 years of age or older
You may not qualify if:
- Not agreeing to participate in the study
- Not being a medical faculty student
- Being unable to understand Turkish
- Being under 18 years of age
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- BENGİSU KARAGÖZlead
Study Sites (1)
Eskisehir Osmangazi University Faculty of Medicine
Eskişehir, Eskişehir, 26040, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
August 6, 2026
First Posted
August 12, 2026
Study Start
July 13, 2026
Primary Completion
August 1, 2026
Study Completion
August 1, 2026
Last Updated
August 12, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share