Young Adult Food Messaging Experiment

August 14, 2026 updated by: Anna Grummon, Stanford University

An Experiment Evaluating the Effectiveness of Counter-marketing Food Messages Among Young Adults

The primary objective of this study is to identify the food counter-marketing messages (i.e., messages that describe deceptive marketing tactics used by food companies) that are perceived as most effective among young adults.

Study Overview

Detailed Description

Participants will complete a within-subjects, randomized experiment in which they view and rate messages describing deceptive marketing tactics used by food companies to sell unhealthy products.

Messages cover five topics: (1) lying about unhealthy products being healthy, (2) engineering foods to be addictive, (3) covering up evidence about the harms of consuming unhealthy products, (4) targeting groups, (5) piggybacking on social causes to promote products. Each topic is presented in five framing variants: an unframed version and four values-based frames that connect the message to a value (e.g., authenticity, fairness). Participants also view one control message, for a total of 26 messages (5 topics × 5 framing variants, plus 1 control).

Topic order is randomized across participants; within each topic, the five framing variants are presented consecutively in random order.

Study Type

Interventional

Enrollment (Estimated)

645

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 Locations

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age between 18-29 years
  • Reside in the United States
  • Consume at least 5-6 servings per week of sugary drinks and 5-6 servings per week of sweet and salty snacks

Exclusion Criteria:

  • Younger than 18 or older than 29 years
  • Reside outside of the United States
  • Consume less than 5-6 servings per week of sugary drinks or less than 5-6 servings per week of sweet and salty snacks

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental: Counter-marketing food messages

Participants view 26 messages. Messages cover five counter-marketing topics: (1) lying about unhealthy products being healthy, (2) engineering foods to be addictive, (3) covering up evidence about the harms of consuming unhealthy products, (4) targeting groups, (5) piggybacking on social causes to promote products. Each topic is presented in five framing variants: an unframed version and four values-based frames that connect the message to a value (e.g., authenticity, fairness). Participants also view one control message, for a total of 26 messages (5 topics × 5 framing variants, plus 1 control).

Topic order is randomized across participants; within each topic, the five framing variants are presented consecutively in random order.

Participants will view 5 messages about how food companies promote unhealthy foods as healthy.
Participants will view 5 messages about how food companies engineer foods to be addictive.
Participants will view 5 messages about how food companies target some groups to sell their unhealthy products.
Participants will view 5 messages about how food companies promote their unhealthy products by piggybacking on popular social causes.
Participants will view 5 messages about how food companies cover up evidence about the harms of their unhealthy products.
Participants will view 1 control message about fire safety.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived message effectiveness for discouraging consumption of unhealthy foods
Time Frame: The survey will take up to 15 minutes
The study will assess perceived message effectiveness for discouraging consumption of sugary drinks and processed snacks with 1 item: "This message discourages me from wanting to consume sugary drinks and processed snacks." Response options for all items will range from "Not at all" (coded as 1) to "A great deal" (coded as 5). Higher scores indicate higher perceived message effectiveness. The survey will measure perceived message effectiveness immediately after participants are exposed to each message.
The survey will take up to 15 minutes

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Anna H. Grummon, Stanford School of Medicine

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)

January 8, 2027

Primary Completion (Estimated)

January 16, 2027

Study Completion (Estimated)

January 16, 2027

Study Registration Dates

First Submitted

August 12, 2026

First Submitted That Met QC Criteria

August 14, 2026

First Posted (Actual)

August 17, 2026

Study Record Updates

Last Update Posted (Actual)

August 17, 2026

Last Update Submitted That Met QC Criteria

August 14, 2026

Last Verified

August 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 85135
  • R01DK142823 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

We will post supporting information to a public repository (e.g., GitHub or similar) upon publication of manuscripts using these data.

IPD Sharing Time Frame

We will post supporting information upon publication of manuscripts using these data.

IPD Sharing Access Criteria

Anyone will be able to access the supporting information.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • 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.

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