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Not yet recruiting Not applicable Interventional Accepts healthy volunteers

Testing Ultra-processed Warning Labels and Not-Ultra-processed Labels in United States

ClinicalTrials.gov ID: NCT07863570

Public ClinicalTrials.gov record NCT07863570. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 13, 2026, 9:48 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Testing Adding Ultra-processed Warning Labels and Not-Ultra-Processed Labels in the FDA Nutrition Info Box, a Randomized Online Experiment in Adults in the United States

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized controlled online experiment will test whether adding an ultra-processed food (UPF) warning label or a positive not-ultra-processed (Not-UPF) label, to the FDA's proposed Nutrition Information Box (NIB) changes consumer perceptions of UPFs among U.S. adults. Participants will be randomized to one of four label conditions and will evaluate UPF and Not-UPF products with different nutritional profiles of 3 food categories: yogurts, cereals, and sliced breads. The primary outcome is shelf choice and the secondary outcomes are correct identification of UPF products, perceived healthfulness, perceived usefulness, and perceived message effectiveness. This experiment aims to answer the following questions: Do UPF warning labels and Not-UPF labels shift shelf choice toward Not-UPF products compared to the NIB alone? Is a UPF warning label more effective than a Not-UPF label at shifting shelf choice, decreasing perceived healthfulness, improving correct identification of UPFs, and increasing perceived usefulness and perceived message effectiveness? Researchers will compare outcomes across the four randomized arms to estimate the independent effect of adding a UPF warning label versus a Not-UPF label beyond nutrient disclosure in the NIB alone.

Study identification

NCT ID
NCT07863570
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Enrollment
12,400 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2026 (Estimated)
Primary completion
Nov 11, 2026 (Estimated)
Completion
Nov 11, 2026 (Estimated)
Last update posted
Oct 8, 2026

2026

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Johns Hopkins Bloomberg School of Public Health Baltimore Maryland 21205 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07863570, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 8, 2026 · Synced Oct 13, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07863570 live on ClinicalTrials.gov.

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