Study Results
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View full resultsBasic Information
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COMPLETED
NA
1252 participants
INTERVENTIONAL
2022-03-16
2023-03-04
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
PREVENTION
DOUBLE
Study Groups
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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.
Racially Congruent Ads
Facebook food ads that are racially congruent.
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.
Racially Incongruent Ads
Facebook food ads that are racially incongruent.
Interventions
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Racially Congruent Ads
Facebook food ads that are racially congruent.
Racially Incongruent Ads
Facebook food ads that are racially incongruent.
Eligibility Criteria
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Inclusion Criteria
* who identifies as only non-Latino White or only Black/African American
* who logs into Facebook once daily
* who can read and speak English
Exclusion Criteria
13 Years
17 Years
ALL
Yes
Sponsors
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National Institutes of Health (NIH)
NIH
National Cancer Institute (NCI)
NIH
NYU Langone Health
OTHER
Responsible Party
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Principal Investigators
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Marie Bragg, PhD
Role: PRINCIPAL_INVESTIGATOR
NYU Langone Health
Locations
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NYU Langone Health
New York, New York, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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20-01796-1
Identifier Type: -
Identifier Source: org_study_id
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