Effects of Racial Congruence, "Likes", and Food Images in Social Media Ads on Adolescents' Caloric Intake - Study 3

June 8, 2026 updated by: NYU Langone Health

Comparing the Effects of Racial Congruence, "Likes," and Food Images in Social Media Ads on Adolescents' Caloric Intake - Study 3

This is a randomized trial to to test the degree to which visual attention to unhealthy foods, racially congruent people, and/or "likes" in social media ads explains the relationship between ad exposure and calorie intake.

Study Overview

Detailed Description

This is a randomized trial to to test the degree to which visual attention to unhealthy foods, racially congruent people, and/or "likes" in social media ads explains the relationship between ad exposure and calorie intake.

Study Type

Interventional

Enrollment (Estimated)

480

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

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • adolescent (13-17 years of age) who identifies as only non-Latino White or only Black/African American; who logs into Instagram once daily; who can read and speak English

Exclusion Criteria:

  • - participants who do not meet all criteria described above

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: Crossover Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Block 1: Black-Food
Exposure to ads with a Black person featuring a food product
Ads featuring a Black person with a food product
Experimental: Block 2: White-Food
Exposure to ads with a White person featuring a food product
Ads featuring a White person with a food product
Experimental: Block 3: Black-Non Food
Exposure to ads with a Black person featuring a non-food product
Ads featuring a Black person with a non-food product
Experimental: Block 4: White-Non Food
Exposure to ads with a White person featuring a non-food product
Ads featuring a White person with a non-food product
Experimental: Block 5: Food-Many Likes
Exposure to ads with many "likes" featuring a food product
Ads with Many "likes" featuring a food product
Experimental: Block 6: Non Food-Many Likes
Exposure to ads with many "likes" featuring a non-food product
Ads with Many "likes" featuring a non-food product
Experimental: Block 7: Food-Few Likes
Exposure to ads with few "likes" featuring a food product
Ads with Few "likes" featuring a food product
Experimental: Block 8: Non Food-Few Likes
Exposure to ads with few "likes" featuring a non-food product
Ads with Few "likes" featuring a non-food product

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Caloric Intake
Time Frame: Day 0 (Approximately 60 minutes)
number of calories consumed during the study protocol
Day 0 (Approximately 60 minutes)
Visual Attention to Ad Features - First Fixation
Time Frame: Day 0 (Approximately 60 minutes)
Measured as time to first fixation to the advertisement.
Day 0 (Approximately 60 minutes)
Visual Attention to Ad Features - Gaze Duration
Time Frame: Day 0 (Approximately 60 minutes)
Measured as the gaze duration during the advertisement.
Day 0 (Approximately 60 minutes)
Visual Attention to Ad Features - Number of Fixations
Time Frame: Day 0 (Approximately 60 minutes)
Measured as the number of fixations on ad features.
Day 0 (Approximately 60 minutes)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Marie A. Bragg, PhD, NYU Langone Health

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)

April 30, 2025

Primary Completion (Estimated)

June 1, 2027

Study Completion (Estimated)

June 1, 2027

Study Registration Dates

First Submitted

May 6, 2025

First Submitted That Met QC Criteria

May 6, 2025

First Posted (Actual)

May 14, 2025

Study Record Updates

Last Update Posted (Actual)

June 10, 2026

Last Update Submitted That Met QC Criteria

June 8, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 20-01796-3
  • R01CA248441 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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