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Study identifier: NCT07531849 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Nutrition Labelling Education Program in Socioeconomically Vulnerable Areas

Condition: Self-Efficacy · Food Choices · Understanding of Front-of-pack Labeling  ·  Sponsor: University of Paris 13

PhaseNA
Planned participants400
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

Front-of-pack nutrition labels (FoPLs) have been adopted in many countries to help consumers rapidly assess the nutritional quality of foods and to encourage healthier choices. Among these schemes, interpretive systems such as Nutri-Score appear particularly promising, as their graphic design improves understanding and use compared with more complex or purely numerical formats. In France, where social inequalities in diet-related chronic diseases are pronounced, implementing and effectively using FoPLs is especially challenging in socioeconomically vulnerable areas. Seine-Saint-Denis, a department with a markedly higher prevalence of diabetes and cardiovascular diseases than the national average, offers a relevant setting to test prevention strategies embedded within routine care. The PEANUTS project is a quasi-experimental before-after interventional study conducted in primary care and hospital outpatient settings, with later extension to the social sector. It aims to evaluate the effectiveness of a brief, literacy-sensitive nutrition education program focused on on-pack nutrition information (Nutri-Score, nutrition facts panel, claims and marketing elements) on self-efficacy, food literacy and the nutritional quality of purchase intentions among adults living in vulnerable territories.

This description comes directly from the study's public registry record.

Talk to the study team

Chantal Julia, MD, PhD  ·  +33148388932  ·  c.julia@eren.smbh.univ-paris13.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Université Sorbonne Paris NordBobigny, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07531849