- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06969651
- Original Trial
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
Status
Recruiting
Conditions
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
- Name: Program Manager
- Phone Number: 6465013880
- Email: krystle.tsai@nyulangone.org
Study Contact Backup
- Name: Zora Hall
- Email: zora.hall@nyulangone.org
Study Locations
-
-
New York
-
New York, New York, United States, 10016
- Recruiting
- NYU Langone Health
-
Contact:
- Program Manager
- Phone Number: 646-501-3394
- Email: krystle.tsai@nyulangone.org
-
-
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.
Sponsor
Collaborators
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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