- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07249398
Influence of Social Media Ads on Food Choice - Master Protocol
Examining Influence of Social Media Ads on Black and White Adolescents' Food Choices: Master ClinicalTrials.Gov Protocol for Aim 1 (NCT05380505), Aim 2 (NCT06969638) and Aim 3 (NCT06969651).
This is a Master ClinicalTrials.gov Protocol for study 20-01796:
Aim 1: Examining Influence of Social Media Ads on Black and White Adolescents' Food Choices - Study 1 (NCT05380505)
Aim 2: A Randomized Trial to Examine the Influence of "Likes" in Social Media Food Ads on Black and White Adolescents' Food Purchases - Study 2 (NCT06969638)
Aim 3: Comparing the Effects of Racial Congruence, "Likes," and Food Images in Social Media Ads on Adolescents' Caloric Intake - Study 3 (NCT06969651)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
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
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- be 13-17 years of age;
- identify as only non-Latino White or only Black/African American;
- report that they log into Facebook at least once daily; and
- read and speak English.
Exclusion Criteria:
- Any criteria not met as listed above will bar an adolescent from participating in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: (Aim 1) Condition 1: Race Congruent Ads
Participants will complete a 15-minute survey in which they will be randomized to view and rate Facebook food ads associated with their condition.
Then they will complete a food purchasing task in which they will shop in an online store that will display six food items and six beverages.
Finally, they will answer demographic questions (e.g., self-reported height and weight) and view a debriefing summary that describes the full purpose of the study.
|
(Aim 1) Facebook food ads that are racially congruent.
|
|
Experimental: (Aim 1) Condition 2: Race Incongruent Ads
Participants will complete a 15-minute survey in which they will be randomized to view and rate Facebook food ads associated with their condition.
Then they will complete a food purchasing task in which they will shop in an online store that will display six food items and six beverages.
Finally, they will answer demographic questions (e.g., self-reported height and weight) and view a debriefing summary that describes the full purpose of the study.
|
(Aim 1) Facebook food ads that are racially incongruent.
|
|
Experimental: (Aim 2) Black Many Likes
Food ads with many "likes" and featuring Black individuals
|
(Aim 2 and 3) Food ads that feature Black individuals.
(Aim 2 and 3) Food ads that have many "likes"
|
|
Experimental: (Aim 2) Black Few Likes
Food ads with few "likes" and featuring Black individuals
|
(Aim 2 and 3) Food ads that feature Black individuals.
(Aim 2 and 3) Food ads that have few "likes"
|
|
Experimental: (Aim 2) White Many Likes
Food ads with many "likes" and featuring White individuals
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(Aim 2 and 3) Food ads that have many "likes"
(Aim 2 and 3) Food ads that feature White individuals.
|
|
Experimental: (Aim 2) White Few Likes
Food ads with few "likes" and featuring White individuals
|
(Aim 2 and 3) Food ads that have few "likes"
(Aim 2 and 3) Food ads that feature White individuals.
|
|
Experimental: (Aim 3) Block 1: Black-Food
Exposure to ads with a Black person featuring a food product
|
(Aim 2 and 3) Food ads that feature Black individuals.
|
|
Experimental: (Aim 3) Block 2: White-Food
Exposure to ads with a White person featuring a food product
|
(Aim 2 and 3) Food ads that feature White individuals.
|
|
Experimental: (Aim 3) Block 3: Black-Non Food
Exposure to ads with a Black person featuring a non-food product
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(Aim 3) Ads featuring a Black person with a non-food product
|
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Experimental: (Aim 3) Block 4: White-Non Food
Exposure to ads with a White person featuring a non-food product
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(Aim 3) Ads featuring a White person with a non-food product
|
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Experimental: (Aim 3) Block 5: Food-Many Likes
Exposure to ads with many "likes" featuring a food product
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(Aim 2 and 3) Food ads that have many "likes"
|
|
Experimental: (Aim 3) Block 6: Non Food-Many Likes
Exposure to ads with many "likes" featuring a non-food product
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(Aim 3) Ads with Many "likes" featuring a non-food product
|
|
Experimental: (Aim 3) Block 7: Food-Few Likes
Exposure to ads with few "likes" featuring a food product
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(Aim 2 and 3) Food ads that have few "likes"
|
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Experimental: (Aim 3) Block 8: Non Food-Few Likes
Exposure to ads with few "likes" featuring a non-food product
|
(Aim 3) Ads with Few "likes" featuring a non-food product
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Calories Purchased
Time Frame: Day 0 (approximately 15 minutes )
|
Aim 1 Participants only.
|
Day 0 (approximately 15 minutes )
|
|
Number of Calories Purchased
Time Frame: Day 0 (approximately 5 minutes)
|
Aim 2 Participants only.
|
Day 0 (approximately 5 minutes)
|
|
Caloric Intake
Time Frame: Day 0 (approximately 60 minutes)
|
Aim 3 Participants only.
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)
|
Aim 3 Participants only.
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)
|
Aim 3 Participants only.
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)
|
Aim 3 Participants only.
Measured as the number of fixations on ad features.
|
Day 0 (approximately 60 minutes)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attitude Toward Ad
Time Frame: Day 0 (approximately 15 minutes )
|
Aim 1 Participants only.
Attitude will be reported on a Likert scale of 1 to 100 (1 = likeable, 100 = unlikeable).
The higher the score, the less likeable the ad is to the participant.
|
Day 0 (approximately 15 minutes )
|
|
Time Spent Viewing Ad
Time Frame: Day 0 (approximately 15 minutes )
|
Aim 1 Participants only.
|
Day 0 (approximately 15 minutes )
|
|
Attitude Toward Ad
Time Frame: Day 0 (approximately 5 minutes)
|
Aim 2 Participants only.
Attitude will be reported on a Likert scale of 1 to 100 (1 = likeable, 100 = unlikeable).
The higher the score, the less likeable the ad is to the participant.
|
Day 0 (approximately 5 minutes)
|
|
Engagement with Ads
Time Frame: Day 0 (approximately 5 minutes)
|
Aim 2 Participants only.
Participants indicate in which ways, if any, they would engage with each ad by answering the following question: "How you would respond if you saw this ad on social media"?
[Select all that apply: "Like" [heart icon and other emojis], comment, tag a friend, direct message a friend, re-post, none of the above]).
The outcome is measured as the number of participants who indicate they would engage with ads.
|
Day 0 (approximately 5 minutes)
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Marie A. Bragg, PhD, NYU Langone Health
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20-01796
- R01CA248441 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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