ClinicalTrials.gg
CompletedNCT03336151Updated Jun 13, 2019

FOP Nutrition Label in Campus Cafeteria

An interventional study of Front-of-pack labelling Nutri-Score in Food Labelling, sponsored by University of Paris 13. Completed at 1 site in France. Per ClinicalTrials.gov, last updated 2019-06-13.

Sponsored by University of Paris 13 · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
119,219
Allocation
Not applicable
Sex
All
01

Study summary

This study evaluates the impact of the introduction of a front-of-pack nutrition label on foods and beverages sold in a campus cafeteria in France on the nutritional quality of purchases.

Read the detailed description

The introduction of front-of-package nutrition labelling is thought to help consumers making healthier food choices at the point-of-purchase.

Recently, the French government has selected the Nutri-Score as single front-of-pack nutrition label.

Evaluations of the Nutri-Score suggest it is in helping consumers making healthier choices. However, its impact in vulnerable populations has not yet been tested. Students are thought to be a vulnerable population due to their limited resources and to their unhealthy food choices.

The objective of the present study is to investigate the impact of the introduction of the Nutri-Score in campus cafeterias on the nutritional quality of food purchases. The intervention is conducted during several months, with a control period without front-of-pack nutrition labelling at the beginning of the university year.

Data on purchases is collected regularly through receipts, and the nutritional quality of purchases is evaluated over time between the intervention situation and the control situation.

02

Conditions studied

  • Food Labelling
03

In context

Lead sponsor

University of Paris 13 is the lead sponsor of 15 studies on the registry; 2 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
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

  • All subjects purchasing foods or beverages in the selected campus cafeteria

Exclusion criteria

Exclusion Criteria:

  • None No individual data is collected. Only purchases data is collected (cash register sales data)
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
119,219 participants (actual)

Study arms

  • Experimental
    Front-of-pack labelling Nutri-Score

    Introduction of the Nutri-Score front-of-pack nutrition label on every food and beverage in the campus cafeteria after a control period without food labelling. The implementation of the label is accompanied by a communication campaign towards students in the form of posters and leaflets.

    Behavioral: Front-of-pack labelling Nutri-Score

Interventions

  • BehavioralFront-of-pack labelling Nutri-Score

    Introduction of the Nutri-Score front-of-pack nutrition label on shelf display tags for every food and beverage sold in the cafeteria

06

What researchers measure

Primary outcomes

  1. Overall nutritional quality of purchases

    Overall nutritional quality of purchases evaluated using the Food Standard Agency nutrient profiling system

    Time frame: Every 15 days, up to 6 months

Secondary outcomes

  1. Energy content of purchases

    Energy content of the purchases (kcal/100g)

    Time frame: Every 15 days, up to 6 months

  2. Saturated fat content of purchases

    Saturated fat content of the purchases (g/100g)

    Time frame: Every 15 days, up to 6 months

  3. Sugar content of purchases

    Sugar content of the purchases (g/100g)

    Time frame: Every 15 days, up to 6 months

  4. Sodium content of purchases

    Sodium content of the purchases (g/100g)

    Time frame: Every 15 days, up to 6 months

  5. Fiber content of purchases

    Fiber content of the purchases (g/100g)

    Time frame: Every 15 days, up to 6 months

  6. Protein content of purchases

    Protein content of the purchases (g/100g)

    Time frame: Every 15 days, up to 6 months

07

Study locations

1 site
  • CROUS Nice - Toulon
    Nice, France
08

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 reached

Ran from Sep 2017 to primary completion in Jun 2018, 9 months.

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

Registered
Nov 3, 2017
First posted
Nov 8, 2017
StartActual
Sep 8, 2017
Primary completionActual
Jun 8, 2018
CompletionActual
Jun 8, 2018
Last update
Jun 13, 2019
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 Jun 13, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03336151
Lead sponsor
University of Paris 13
Responsible party
Serge HERCBERG (Head of Department, University of Paris 13) — Principal investigator
First posted
Nov 8, 2017
Start date
Sep 8, 2017
Primary completion
Jun 8, 2018
Completion
Jun 8, 2018
Last update
Jun 13, 2019

Oversight

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

Not currently enrolling

This study is completed, as verified in Jun 2019. You cannot join it, but the record below documents what was studied.

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