NSS Grocery Store Brazil

April 13, 2026 updated by: Allison Sylvetsky (Meni), George Washington University

Effects of a Non-sugar Sweetener Label on Parents' Selection of Foods and Beverages in Brazil: a Randomized Clinical Trial.

The purpose of this study is to assess the impact of non-sugar sweeteners (NSS) front-of-package labels (FOPL) on Brazilian parents' food and beverage selections for their children. The study includes three arms: 1. no NSS FOPL control group, 2. a group exposed to a NSS FOPL modeled after the Mexican warning label for NSS, and 3. a group exposed to a NSS FOPL using the magnifying glass symbol currently implemented in Brazil for nutrients of public health concern. Participants will be instructed to select products for their child, including one yogurt, three beverages (for breakfast, lunch, and dinner), one granola, and one cereal bar.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

1068

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • District of Columbia
      • Washington D.C., District of Columbia, United States, 20037
        • Recruiting
        • Milken Institute School of Public Health
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Eligible participants include:

  • Adults aged 20 years or older,
  • Living in Brazil
  • Parents or guardians of children between 2 and 12 years old
  • Primarily responsible for the household grocery shopping (more than 50%)
  • Can read and understand Portuguese

Recruitment will occur nationwide through an online panel, with quotas for education, race, and geographic distribution to approximate the national profile.

Individuals will be excluded if

  • Not a parent or guardian of a child aged 2-12 years
  • Younger than 20 years
  • Not primarily responsible for more than half of the household grocery shopping
  • Unable to read or understand Portuguese
  • Do not provide informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Participants view the online store without any non-sugar sweetener front-of-package label
Experimental: Mexico-based NSS FOPL
Participants view the online store with the Mexican-style non-sugar sweetener front-of-package label on eligible products
Participants view the online store with the Mexican-style non-sugar sweetener front-of-package label on eligible products
Experimental: Brazil-based NSS FOPL
Participants view the online store with the magnifying glass non-sugar sweetener front-of-package label like the one used in Brazil
Participants view the online store with the magnifying glass non-sugar sweetener front-of-package label like the one used in Brazil

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percentage of products selected that are unsweetened or low in added sugars
Time Frame: Day 1
Selection of products that do not contain NSS or added sugars, or that contain added sugars below the FOPL threshold (i.e., less than 10 g per 100 g) for granola and cereal bars.
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percentage of products selected that contain NSS and high added sugars
Time Frame: Day 1
Selection of products containing both NSS and are high in added sugars, defined as those displaying the FOPL for added sugars (i.e., more than 7.5 g per 100 ml for liquids, and more than 10 g per 100 g for foods).
Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 15, 2026

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

June 30, 2026

Study Registration Dates

First Submitted

September 15, 2025

First Submitted That Met QC Criteria

November 21, 2025

First Posted (Actual)

November 25, 2025

Study Record Updates

Last Update Posted (Actual)

April 15, 2026

Last Update Submitted That Met QC Criteria

April 13, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • FWA00005945

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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