Effects of UPF Warning Labels on Social Media Among Teens and Young Adults

November 24, 2025 updated by: Yuru Huang, University of Tennessee

Online Randomized Experiment Evaluating Ultra-Processed Food Warning Labels on Social Media Posts Among Teens and Young Adults

This study aims to evaluate whether Ultra-Processed Food (UPF) warning labels on social media posts improve consumer understanding and influence purchase intentions among teens and young adults. Participants aged 13-29 in the United States will be recruited and randomized into two groups: a control group (no label) and an intervention group (UPF warning). Participants will view social media posts featuring UPFs with or without warning labels and respond to survey questions following each post.

Study Overview

Detailed Description

This study is designed to assess the effect of a highly visible UPF warning label on social media posts among adolescents and young adults in the United States. we will recruit approximately 500 US teens aged 13-17 and 500 young adults aged 18-29.

Participants will complete a between-subjects online randomized experiment. They will be randomized into either a UPF warning label group or a no label control group. Participants will view four social media posts featuring UPFs (with or without warning labels based on their assigned group) in random order. These posts are based on real Instagram advertisements from leading food and beverage companies; two posts will feature sugar-sweetened beverages and two will feature fast-food menu items. After viewing each post, participants will answer questions assessing consumer understanding, purchase intentions, and perceived healthfulness. At the end of the survey, all participants will also respond to questions regarding perceptions of control over healthy eating, policy support for UPF warnings, and their understanding of the term "ultra-processed food."

Study Type

Interventional

Enrollment (Estimated)

1000

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

    • Tennessee
      • Memphis, Tennessee, United States, 38163
        • UTHSC Department of Preventive Medicine
        • 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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Aged 13-29
  • Reside in the US
  • Can read and speak English

Exclusion Criteria:

  • Under the age of 13 or over 29
  • Reside outside of the United States
  • Unable to complete a survey in English

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: UPF Warning Labels
UPF warning labels will be placed beneath each social media post. Each label will feature an icon accompanied by explanatory text, using the exact health risk wording proposed in the Childhood Diabetes Reductions Act: "Warning: consuming ultra-processed foods and drinks can cause weight gain, which increases the risk of obesity and type-2 diabetes". All text will be left-aligned. The icon will consist of exclamation marks within a yellow triangle. The warning label will be large and highly visible and enclosed within a bold rectangular border.
Participants will view four Instagram posts featuring UPFs, displayed with warning labels
Other: No Label (Control)
No label
Participants will view four Instagram posts featuring UPFs, displayed without warning labels

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Consumer understanding
Time Frame: Assessed during one-time 10-minute online study survey
For each social media post, participants will be asked whether they think the product is ultra-processed. Response options will be "yes", "no", or "I don't know". Consumer understanding will be coded as a binary outcome: "yes" = correct; "no" and "I don't know" = incorrect.
Assessed during one-time 10-minute online study survey
Purchase intentions
Time Frame: Assessed during one-time 10-minute online study survey
For each social media post, participants will be asked how likely they would buy the product in the next week, either in-store or online. Response options will be on a 1-5 Likert scale, with 5 being "very likely". Higher scores indicate higher intentions to purchase the product.
Assessed during one-time 10-minute online study survey

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived healthfulness
Time Frame: Assessed during one-time 10-minute online study survey
For each social media post, participants will be asked how healthy the product seems to them. Responses options will be on a 1-5 Likert scale, with 5 indicating "very healthy". Higher scores indicate higher perceived healthfulness.
Assessed during one-time 10-minute online study survey
Perceptions of control over healthy eating
Time Frame: Assessed during one-time 10-minute online study survey
After viewing all four social media posts, all participants will be shown the UPF warning label (regardless of condition) and asked whether the UPF warning labels make them feel "less in control of making healthy eating decision," "neither less nor more in control or making healthy eating decisions," or "more in control of making healthy eating decisions." Responses will be binary coded: "more in control" = 1; "less" or "neither" = 0.
Assessed during one-time 10-minute online study survey
Policy support for ultra-processed food warning labels
Time Frame: Assessed during one-time 10-minute online study survey
After viewing all four social media posts, all participants will be shown the UPF warning label (regardless of condition) and asked whether they support or oppose a policy requiring these labels on social media advertisements for ultra-processed foods and beverages. Response options will be on a 1-5 Likert scale, with 5 indicating "Strongly support." Higher scores will indicate higher support for warning labels.
Assessed during one-time 10-minute online study survey

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Yuru Huang, University of Tennessee
  • Principal Investigator: Anna Grummon, Stanford University

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 (Estimated)

December 1, 2025

Primary Completion (Estimated)

December 20, 2025

Study Completion (Estimated)

December 20, 2025

Study Registration Dates

First Submitted

November 10, 2025

First Submitted That Met QC Criteria

November 11, 2025

First Posted (Estimated)

November 12, 2025

Study Record Updates

Last Update Posted (Actual)

December 2, 2025

Last Update Submitted That Met QC Criteria

November 24, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 25-10909-NHSR

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Investigators will post de-identified individual participant data in a public repository.

IPD Sharing Time Frame

Investigators will post IDP within 6 months of publication of manuscripts associated with the data generated in this study.

IPD Sharing Access Criteria

Data and code will be made publicly available.

IPD Sharing Supporting Information Type

  • SAP
  • ANALYTIC_CODE

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.

Clinical Trials on Food Preferences

Clinical Trials on UPF Warning Labels

Subscribe