- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05953194
Effects of Sugary Drinks Counter-marketing Messages
February 26, 2024 updated by: Anna Grummon, Stanford University
Effects of Anti-sugar-sweetened-beverage Counter-marketing on Behavioral Intentions and Perceived Weight Stigma
This study aims to examine consumer responses to traditional and counter-marketing messages discouraging sugary drink consumption, including effects on intentions to consume sugary drinks and perceived weight stigma.
Because prior research has suggested that counter-marketing may be especially effective among younger populations, the investigators will examine effects overall and by age group (young adults [ages 18-29 years] vs. middle and older adults [ages 30+ years]).
Study Overview
Status
Completed
Conditions
Detailed Description
In this online randomized clinical trial, participants will be randomized to one of three arms: 1) Control (neutral) messages, 2) Traditional health messages, and 3) Counter-marketing messages.
In each arm, participants will view four messages developed for their randomly assigned arm and answer questions about the messages and their behavioral intentions.
Study Type
Interventional
Enrollment (Actual)
2184
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 Locations
-
-
California
-
Palo Alto, California, United States, 94304
- Stanford School of Medicine
-
-
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
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- 18 years old or older
Exclusion Criteria:
- Less than 18 years old
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: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Traditional health messages
Participants will view traditional health messages focused on the health consequences of sugar-sweetened beverage consumption, using text adapted from prior sugary drink campaigns.
Participants will view a total of 4 messages developed for this arm.
|
Traditional health messages focused on the health consequences of sugar-sweetened beverage consumption, using text adapted from prior sugary drink campaigns.
Participants will view a total of 4 messages developed for this arm.
|
|
Active Comparator: Control (neutral) messages
Participants will view control messages approximately matched to the intervention messages on length, but discussing a neutral topic unrelated to sugary drinks (safe driving).
Participants will view a total of 4 messages developed for this arm.
|
Control messages approximately matched to the intervention messages on length, but discussing a neutral topic unrelated to sugary drinks (safe driving).
Participants will view a total of 4 messages developed for this arm.
|
|
Experimental: Counter-marketing messages
Participants will view counter-marketing messages about sugary drinks that incorporate principles of effective counter-marketing campaigns, including describing industry manipulation of consumers, appealing to emotions (especially anger), describing health consequences, and criticizing the industry for demographic targeting.
Messages include text adapted from prior counter-marketing campaigns.
Participants will view a total of 4 messages developed for this arm.
|
Counter-marketing messages about sugary drinks that incorporate principles of effective counter-marketing campaigns, including describing industry manipulation of consumers, appealing to emotions (especially anger), describing health consequences, and criticizing the industry for demographic targeting.
Messages include text adapted from prior counter-marketing campaigns.
Participants will view a total of 4 messages developed for this arm.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intentions to consume sugary drinks
Time Frame: The survey will take up to 20 minutes
|
We will assess intentions to consume sugary drinks using 2 items: "In the next week, I plan to drink sugary drinks like sodas, sports drinks, or fruit drinks," and "In the next week, I am likely to drink sugar-sweetened beverages like sodas, sports drinks, or fruit drinks".
Response options to both items will use a 5-point Likert scale: the first item's response options will range from "definitely not" (1) to "definitely yes" (5), and the second item's response options will range from "not at all likely" (1) to "extremely likely" (5).
We will average responses to the 2 items.
|
The survey will take up to 20 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived message effectiveness for discouraging sugary drink consumption
Time Frame: The survey will take up to 20 minutes
|
Item: "These messages discourage me from wanting to drink sugary drinks."
This variable will be measured on a 5-point Likert scale ranging from "not at all" (1) to "a great deal" (5).
|
The survey will take up to 20 minutes
|
|
Negative feelings toward drinking sugary drinks
Time Frame: The survey will take up to 20 minutes
|
Item: "How do these messages make you feel about drinking sugary drinks?"
This variable will be measured on a 5-point Likert scale ranging from "extremely positive" (1) to "extremely negative" (5).
|
The survey will take up to 20 minutes
|
|
Anticipated social interactions
Time Frame: The survey will take up to 20 minutes
|
We will examine anticipated social interactions by asking, "How likely are you to talk about these messages with others in the next week?"
This item will be scored on a 5-pt Likert scale ranging from "not at all likely" (1) to "extremely likely" (5).
|
The survey will take up to 20 minutes
|
|
Attitudes toward sugary drink companies
Time Frame: The survey will take up to 20 minutes
|
We will examine attitudes toward sugary drink companies by asking, "How do you feel about companies that make sugary drinks?"
This item will be scored on a 5-pt Likert scale ranging from "dislike them a lot" (1) to "like them a lot" (5).
|
The survey will take up to 20 minutes
|
|
Perceived obesity stigma
Time Frame: The survey will take up to 20 minutes
|
We will examine the extent to which participants perceive the messages as contributing to obesity stigma by asking 3 items: "These messages promote negative attitudes about people who have overweight or obesity," "These messages increase blame towards people for being overweight," and "These messages make obesity seem like a much simpler issue than it really is."
Each item will be scored on a 5-point Likert scale from "not at all" (1) to "a great deal" (5).
We will average responses to these items.
|
The survey will take up to 20 minutes
|
|
Message reactance
Time Frame: The survey will take up to 20 minutes
|
We will examine psychological reactance to the messages by asking 3 items: "These messages are trying to manipulate me," "These messages are overblown" and "How much do these messages make you feel angry?"
Each item will be scored on a 5-point Likert scale from "not at all" (1) to "a great deal" (5).
We will average responses to these items, assuming sufficient internal consistency (alpha>=.70).
|
The survey will take up to 20 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Anna H Grummon, PhD, Stanford School of Medicine, Department of Pediatrics
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Bryan CJ, Yeager DS, Hinojosa CP. A values-alignment intervention protects adolescents from the effects of food marketing. Nat Hum Behav. 2019 Jun;3(6):596-603. doi: 10.1038/s41562-019-0586-6. Epub 2019 Apr 15.
- Kraak VI, Consavage Stanley K, Harrigan PB, Zhou M. How have media campaigns been used to promote and discourage healthy and unhealthy beverages in the United States? A systematic scoping review to inform future research to reduce sugary beverage health risks. Obes Rev. 2022 May;23(5):e13425. doi: 10.1111/obr.13425. Epub 2022 Feb 9.
- Boles M, Adams A, Gredler A, Manhas S. Ability of a mass media campaign to influence knowledge, attitudes, and behaviors about sugary drinks and obesity. Prev Med. 2014 Oct;67 Suppl 1:S40-5. doi: 10.1016/j.ypmed.2014.07.023. Epub 2014 Jul 24.
- Kite J, Grunseit A, Bohn-Goldbaum E, Bellew B, Carroll T, Bauman A. A Systematic Search and Review of Adult-Targeted Overweight and Obesity Prevention Mass Media Campaigns and Their Evaluation: 2000-2017. J Health Commun. 2018;23(2):207-232. doi: 10.1080/10810730.2018.1423651. Epub 2018 Jan 16.
- Te V, Ford P, Schubert L. Exploring social media campaigns against sugar-sweetened beverage consumption: A systematic search. Schumacher U, ed. Cogent Medicine. 2019;6(1):1607432. doi:10.1080/2331205X.2019.1607432
- Crandall CS, Reser AH. Attributions and Weight-Based Prejudice. In: Brownell K, Puhl R, Schwartz M, Rudd L, eds. Weight Bias: Nature, Consequences, and Remedies. Guilford Publications; 2005:83-96.
- Puhl RM, Schwartz MB, Brownell KD. Impact of perceived consensus on stereotypes about obese people: a new approach for reducing bias. Health Psychol. 2005 Sep;24(5):517-25. doi: 10.1037/0278-6133.24.5.517.
- Dixon H, Scully M, Gascoyne C, Wakefield M. Can counter-advertising diminish persuasive effects of conventional and pseudo-healthy unhealthy food product advertising on parents?: an experimental study. BMC Public Health. 2020 Nov 25;20(1):1781. doi: 10.1186/s12889-020-09881-1.
- Krieger J, Kwon T, Ruiz R, Walkinshaw LP, Yan J, Roberto CA. Countermarketing About Fruit Drinks, Alone or With Water Promotion: A 2019 Randomized Controlled Trial in Latinx Parents. Am J Public Health. 2021 Nov;111(11):1997-2007. doi: 10.2105/AJPH.2021.306488. Epub 2021 Oct 28.
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)
August 7, 2023
Primary Completion (Actual)
August 7, 2023
Study Completion (Actual)
August 7, 2023
Study Registration Dates
First Submitted
July 11, 2023
First Submitted That Met QC Criteria
July 11, 2023
First Posted (Actual)
July 20, 2023
Study Record Updates
Last Update Posted (Estimated)
February 28, 2024
Last Update Submitted That Met QC Criteria
February 26, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 69580a
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The investigators will share statistical analysis plan and analytic code after publication.
The investigators will post these items and de-identified data on ResearchBox, a publicly available platform.
IPD Sharing Time Frame
Within 6 months of publication
IPD Sharing Access Criteria
There will be no access criteria; information will be publicly available.
We plan to make these resources available on ResearchBox.
IPD Sharing Supporting Information Type
- 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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