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Active, not recruitingNCT07761559Updated Aug 12, 2026

Effect of a Nutrition Education Intervention on Ultra-Processed Food Awareness and Consumption Among University Students

An interventional study of Structured Nutrition Education Program on Ultra-Processed Foods in Ultra-Processed Food Consumption, Nutrition Knowledge and Ultra-processed Food, sponsored by BENGİSU KARAGÖZ. Active, not recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-12.

Sponsored by BENGİSU KARAGÖZ · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Aug 2026, 3 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
74
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

This study is designed as a cluster-randomized controlled intervention study with pre-intervention, post-intervention, and one-month follow-up measurements. The study will be conducted among sixth-year medical students at Eskisehir Osmangazi University Faculty of Medicine. Students aged 18 years or older who understand Turkish, agree to participate, and provide informed consent will be eligible.

Internship groups will be assigned as clusters to either the intervention group or the control group. All eligible students in the selected internship groups will be invited to participate. The sample size calculation indicated that at least 34 participants per group are required. To account for possible losses during follow-up, the target sample size was increased by 10%. The final number of participants may vary depending on the number of eligible and consenting students in the selected clusters.

The intervention group will receive a structured nutrition education program, while the control group will not receive this program during the study period. The education program is based on the Health Belief Model and Social Cognitive Theory. It focuses on ultra-processed foods, the NOVA food classification system, associations between ultra-processed food consumption and chronic diseases, nutrition label literacy, food security, nutrition self-efficacy, and healthier food choices.

The program includes lectures, small-group discussions, interactive quizzes, case-based learning, role-playing, food-label exercises, analysis of dietary records, low-cost meal planning, and practical cooking activities. Participants will learn to distinguish ultra-processed foods from minimally processed and processed foods, interpret ingredient lists and nutrition information, evaluate the contribution of ultra-processed foods to dietary energy and nutrient intake, and establish achievable personal goals for reducing ultra-processed food consumption.

Data will be collected at baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2). The assessment includes sociodemographic characteristics and health behaviors, food security, knowledge and attitudes concerning ultra-processed foods, food-processing knowledge, ultra-processed food consumption, nutrition label literacy, nutrition self-efficacy, and three-day dietary records.

Changes in outcomes over time will be compared between the intervention and control groups to determine whether the education program improves knowledge, attitudes, nutrition label literacy, and nutrition self-efficacy and reduces ultra-processed food consumption.

02

Conditions studied

  • Ultra-Processed Food Consumption
  • Nutrition Knowledge
  • Ultra-processed Food
  • Food Insecurity
  • Nutrition Label Literacy
  • Front-of-Pack Nutrition Labeling

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Keywords

  • Ultra-Processed Foods
  • Nutrition Education
  • Nutrition Label Literacy
  • Food Insecurity
  • Nutrition Self-Efficacy
  • Medical Students
  • Cluster-Randomized Trial
  • Front-of-Pack Nutrition Labeling
03

In context

Literacy

201 studies on the registry are indexed under Literacy; 69 are open to participants now.

This study's planned enrollment of 74 is below the median of 124 across 170 interventional studies indexed under Literacy.

Browse Literacy studies →

Lead sponsor

This is the only study on the registry with BENGİSU KARAGÖZ as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Agreeing to participate in the study
  • Being a medical faculty student
  • Being able to understand Turkish
  • Being 18 years of age or older

Exclusion criteria

Exclusion Criteria:

  • Not agreeing to participate in the study
  • Not being a medical faculty student
  • Being unable to understand Turkish
  • Being under 18 years of age
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
74 participants (estimated)

Study arms

  • Experimental
    Nutrition Education Intervention

    Participants 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.

    Behavioral: Structured Nutrition Education Program on Ultra-Processed Foods

  • No intervention
    Control Group

    Participants 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

  • BehavioralStructured Nutrition Education Program on Ultra-Processed Foods

    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

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

  2. 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.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

Secondary outcomes

  1. Change in Food Processing Knowledge

    Food processing knowledge will be assessed using the Food Processing Knowledge Score (FoodProK). The assessment includes 12 foods from four categories: fruits, meat products, dairy products, and grains. Each category includes foods representing NOVA Groups 1, 3, and 4. Participants rank the foods according to perceived healthiness. Each category is scored from 0 to 2 according to agreement with the expected NOVA-based ranking. The total score ranges from 0 to 8, with higher scores indicating greater knowledge of food processing levels.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

  2. Change in Nutrition Label Literacy

    Nutrition label literacy will be assessed using the 10-item Evaluation and Application of Label Information subscale of the Food Label Literacy Scale. Items are scored on a 5-point Likert scale ranging from 1 (very difficult) to 5 (very easy). Higher scores indicate greater nutrition label literacy.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

  3. Change in Nutrition Self-Efficacy

    Nutrition self-efficacy will be assessed using the five-item Nutrition Self-Efficacy Scale. Each item is scored on a 4-point Likert scale ranging from 1 (not at all certain) to 4 (very certain). No items are reverse-scored. The total score ranges from 5 to 20, with higher scores indicating greater nutrition self-efficacy.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

  4. Change in the Acceptability of Front-of-Pack Nutrition Labels

    The acceptability of front-of-pack nutrition labels will be assessed using five items adapted from previous studies. Each item is scored on a 5-point Likert scale. The mean score of the five items will be calculated, with higher mean scores indicating greater acceptability of front-of-pack nutrition labels.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

  5. Change in Purchase Intention for Products With Front-of-Pack Nutrition Labels

    Purchase intention for products displaying front-of-pack nutrition labels will be assessed using one item scored on a 5-point Likert scale.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

  6. Change in Views About Front-of-Pack Nutrition Labels

    Participants' views about front-of-pack nutrition labels will be assessed using three items adapted from previous studies. Each item is scored on a 5-point Likert scale.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

  7. Change in Dietary Intake Based on Three-Day Food Records

    Dietary intake will be assessed using three-day food records completed by the participants. The records will cover two weekdays and one weekend day, with all foods and beverages consumed during each 24-hour period recorded by the participants.

    Time frame: Baseline before the intervention (T0), immediately after the intervention (T1), and at the one-month follow-up (T2)

07

Study locations

1 site
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2026 (actual). Primary completion is estimated for Aug 2026, 1 month after the start.

Of 115 non-industry interventional studies with no phase under Literacy, half reached primary completion within 11 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 20. This study's planned 1 month is below that.

Counting every sponsor, half of 117 studies reached it within 11 months; a quarter within 4 and three quarters within 19.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 6, 2026
First posted
Aug 12, 2026
StartActual
Jul 13, 2026
Primary completionEst.
Aug 2026
CompletionEst.
Aug 2026
Last update
Aug 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07761559
Lead sponsor
BENGİSU KARAGÖZ
Responsible party
BENGİSU KARAGÖZ (Research Assistant, Eskisehir Osmangazi University) — Sponsor-investigator
First posted
Aug 12, 2026
Start date
Jul 13, 2026
Primary completion
Aug 2026 (estimated)
Completion
Aug 2026 (estimated)
Last update
Aug 12, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is active, not recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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