- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04252898
Impact of a Front-of-pack Nutrition Labelling on Food Purchases in Contract Catering
Impact of a Front-of-pack Nutrition Labelling on the Nutritional Quality of Purchases of Customers in Contract Catering - a Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The introduction of front-of-pack nutrition labelling is thought to help consumers making healthier food choices at the point-of-purchase. In 2017, the French government has selected the Nutri-Score as single front-of-pack nutrition label to be applied on food products sold in French supermarkets, on a voluntary basis.
Some studies have found that the Nutri-Score would help consumers making healthier choices. Nevertheless, its impact has been demonstrated in experimental supermarkets and its implementation only concerns products sold in groceries and supermarkets, as it is stated in the official decree. The potential impact of the Nutri-Score in contract catering remains unknown, while this sector represents a growing share of out-of-home catering and that the promotion of the Nutri-Score in this sector is now part of the National Public Health Plan.
Thus, the objective of the present study is to investigate the impact of the implementation of the Nutri-Score in contract catering restaurants on the nutritional quality of food purchases. The trial will be conducted using a quasi experimental before/after design with a comparison group. Data on purchases will be collected regularly through receipts, and the nutritional quality of purchases will be evaluated over time on two pairs of sites. In each pair of sites, one site will receive an intervention (Nutri-Score) and one site will be a control site. Within each pair, the sites will be comparable in terms of food offer and consumers profile.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Bobigny, France, 93017
- Equipe de recherche en Epidémiologie nutritionnelle
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- all individuals purchasing in the contract catering restaurants will be included.
Exclusion Criteria:
- No
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention arm
In this arm (site n°1), participants will purchase their products in the restaurant first in a control phase and then in an interventional phase with the Nutri-Score affixed on food products.
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The intervention consists of displaying the Nutri-Score on dishes and pre-packed foods.
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No Intervention: Control arm
In this arm (site n°2), participants will purchase their products in the restaurant during the whole study without any label affixed on food products.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in the overall nutritional quality of purchases over time
Time Frame: Through study completion, an average of 6 months
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Score using the Food Standards Agency nutrient profiling system modified by the HCSP, allocating points depending on the amounts in unfavourable elements (energy, saturates, sugars, sodium) and favorable elements (fibres, proteins and fruits, vegetables, nuts and oils (olive, colza, nuts))
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Through study completion, an average of 6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in energy content of purchases
Time Frame: Through study completion, an average of 6 months
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Energy content of the purchases in kcal / 100g
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Through study completion, an average of 6 months
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Change in Saturated fat content of purchases
Time Frame: Through study completion, an average of 6 months
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Saturated fat content of the purchases in g / 100g
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Through study completion, an average of 6 months
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Change in Sugar content of purchases
Time Frame: Through study completion, an average of 6 months
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Sugar content of the purchases in g / 100g
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Through study completion, an average of 6 months
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Change in Sodium content of purchases
Time Frame: Through study completion, an average of 6 months
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Sodium content of the purchases in mg / 100g
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Through study completion, an average of 6 months
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Change in Protein content of purchases
Time Frame: Through study completion, an average of 6 months
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Protein content of the purchases in g / 100g
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Through study completion, an average of 6 months
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Change in Fibre content of purchases
Time Frame: Through study completion, an average of 6 months
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Fibre content of the purchases in g / 100g
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Through study completion, an average of 6 months
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Change in Fruit, vegetable and nut content of purchases
Time Frame: Through study completion, an average of 6 months
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Fruit, vegetable and nut content of the purchases in % / 100g
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Through study completion, an average of 6 months
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Collaborators and Investigators
Sponsor
Collaborators
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
Other Study ID Numbers
- ELIOR
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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