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Social MediaNCT07768488

Evaluating Food Messaging Campaigns for Young Adults

A study testing Counter-marketing and Health education in people with Social Media and Diet Quality, run by Stanford University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study aims to determine whether online social media campaigns improve diet quality among young adults. Young adults will be exposed to one of three social media campaigns. Read more about this study

Who is it for?
Ages 18 to 29 yearsHealthy volunteers can take part
Conditions the study is for
Social Media, Diet Quality, Diet Intervention
What is being tested?
Counter-marketing and Health education
Could I receive a placebo?
No, everyone receives an active treatment
How many people
750 participants
Where
No sites listed yet
Study dates
Sep 2027to Apr 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 29 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 18-29 years old
  • Reside in the US
  • Speak English
  • Use Instagram 3-4 times per week or more
  • Consume sugary drinks 5-6 times per week or more and consume sweet and salty snacks 5-6 times per week or more

Who cannot join

  • Younger than 18 years or older than 29 years
  • Do not reside in the US
  • Do not speak English
  • Use Instagram less than 3-4 times per week
  • Consume sugary drinks less than 5-6 times per week or consume sweet and salty snacks less than 5-6 times per week

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Amanda Food Policy Lab Study Team contact

408-598-2672

foodpolicylab@stanford.edu

About this study

Official title: Evaluating a Counter-marketing Campaign to Improve Diet Quality Among Young Adults

This study aims to determine whether online social media campaigns improve diet quality among young adults. Young adults will be exposed to one of three social media campaigns.

Read the detailed description

In this 3-arm parallel randomized controlled trial, participants will be randomized to one of three arms: 1) Control (neutral) messages, 2) Health education messages that focus on describing the health harms of consuming sugary drinks and processed snack foods, or 3) Counter-marketing messages that focus on exposing and undermining deceptive, harmful, or misleading marketing practices used by food companies to sell unhealthy foods. In each arm, participants will follow private Instagram accounts corresponding to their study arm. The study team will post campaign messages to the Instagram accounts. Participants will complete dietary recalls and answer online survey questions.

Being tested
Counter-marketing, Health education, Control (neutral) messages
Medical subject headings
Communication

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Counter-marketingBehavioural

    Participants will receive messages focused on exposing and undermining deceptive, harmful, or misleading marketing practices used by food companies to sell unhealthy foods. Messages are delivered via Instagram posts.

  • Health educationBehavioural

    Participants will receive messages about the health consequences of sugary drinks and processed snack foods. Messages are delivered via Instagram posts.

  • Control (neutral) messagesBehavioural

    Participants will receive messages describing neutral topic unrelated to food (fire and home safety). Messages are delivered via Instagram posts.

Study groups in NCT07768488
Study groupRoleWhat they receive
Counter-marketing messagesExperimentalParticipants will view a 10-week Instagram-delivered counter-marketing campaign exposing deceptive and harmful marketing practices used by food companies to sell sugary drinks and processed snack foods. Messages are drawn from those identified as most promising in prior message-development research and are targeted to values important to young adults (e.g., autonomy, respect).
Receives: Behavioral: Counter-marketing
Health education messagesExperimentalParticipants will view a 10-week Instagram-delivered health education campaign about the health consequences of sugary drinks and processed snack foods. Messages are adapted from existing public health campaigns about these foods.
Receives: Behavioral: Health education
Control (neutral) messagesActive comparatorParticipants will view a 10-week Instagram-delivered campaign about fire and home safety, a topic unrelated to diet. Messages are adapted from existing public health campaigns about these issues.
Receives: Behavioral: Control (neutral) messages

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Diet quality (Healthy Eating Index-2020 score)

    Overall diet quality calculated from up to two unannounced, nonconsecutive 24-hour dietary recalls (1 weekend day, 1 weekday) collected via NCI's Automated Self-Administered 24-Hour Dietary Assessment Tool (ASA24) at each time point. Healthy Eating Index-2020 scores reflect alignment with the US Dietary Guidelines for Americans; higher scores indicate healthier diet quality (i.e., greater intake of fruits, vegetables, whole grains, dairy, protein, and unsaturated fats and lower intake of saturated fat, sodium, added sugars, and refined grains).

    Measured: At 0-months (baseline), 3-months (immediately post- intervention), and 9-months (6-months post-intervention)

Secondary outcomes (7)
  1. Consumption of target food groups

    Consumption of the food groups targeted in the campaigns (sugary drinks, processed sweet and salty snack foods) will be assessed using two unannounced, nonconsecutive 24-hour dietary recalls (1 weekend day, 1 weekday) collected via NCI's Automated Self-Administered 24-Hour Dietary Assessment Tool (ASA24) at each time point. Servings of each target food group will be calculated and summed such that higher values indicate higher consumption of the target food groups.

    Measured: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)

  2. Internalized weight stigma

    Survey items will assess internalized weight stigma using the 11-item Modified Weight Bias Internalization Scale (e.g., "I am less attractive than most other people because of my weight."). Responses will be measured on 5-point Likert scale ranging from "Strongly disagree" (1) to "Strongly agree" (5). Responses will be coded such that higher scores indicate higher internalized weight stigma. Responses to the 11 items will be averaged.

    Measured: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention).

  3. Disordered eating attitudes and behaviors

    Survey items will assess disordered eating attitudes and behaviors using the Eating Disorder Examination Questionnaire (EDE-Q), a 28-item self-report questionnaire assessing the range, frequency, and severity of disordered eating attitudes and behaviors, including restraint, eating concern, shape concern, and weight concern. Responses will be measured on a 6-point scale, ranging from "No days" or "None of the times" or "Not at all" or "Not at all markedly" (each coded as 0) to "Every day" or "Every time" or "Markedly" or "Moderately" (each coded as 5). Following scoring guidance, global scores will be calculated as follows: analyses will sum responses within each of the 4 subscales (restraint, eating concern, shape concern, and weight concern), divide those scores by the number of items in the subscale, sum the subscale scores, and divide this sum by 4. Higher global scores indicate higher frequency or severity of disordered eating attitudes and behaviors.

    Measured: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)

  4. Attitudes toward unhealthy food companies

    Survey items will assess the extent to which participants feel positively or negatively toward food companies that sell unhealthy foods with 2 items: "How do you feel about companies that sell sugary drinks?" and "How do you feel about companies that sell processed sweet and salty snack foods?" Each item will be measured on a 5-point Likert scale ranging from "Very unfavorably" (1) to "Very favorably" (5). Responses to these items will be averaged. Higher scores indicate more positive attitudes toward unhealthy food companies.

    Measured: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)

  5. Perceived alignment of healthy eating with values

    Survey items will assess the extent to which participants view healthy eating behaviors (such as reducing their sugary drink consumption) as aligned with personal values such as autonomy and respect with two items: "When I limit how much I drink sugary drinks, I'm doing my part to disempower companies that try to cover up scientific evidence" and "When I limit how much I eat sweet and salty snacks, I'm doing my part to disempower companies that try to cover up scientific evidence." Responses will be measured on a 5-point Likert scale ranging from "Strongly disagree"(1) to "Strongly agree" (5). Responses to these items will be averaged. Higher scores indicate higher perceived alignment of healthy eating with values.

    Measured: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)

  6. Externalized weight stigma

    Survey items will assess the extent to which participants hold negative views about people with higher body weight using the 20-item Universal Measure of Bias - Fat Scale (UMB-FAT). Response items will be measured on a 5-point Likert scale ranging from "Strongly agree" (1) to "Strongly disagree" (5). Responses to these items will be averaged. Higher scores indicate higher externalized weight stigma.

    Measured: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)

  7. Attribution of individual responsibility for weight

    Survey items will assess the extent to which participants attribute responsibility for body weight to individuals using the 16-item Causal Attribution for Obesity scale. Response items will be measured on a 5-point Likert scale ranging from "Strongly agree" (1) to "Strongly disagree" (5). Responses to these items will be averaged. Higher scores indicate stronger attribution of responsibility to individuals for their body weight.

    Measured: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Aug 2026
  2. Study startSep 2027 (estimated)
  3. Primary completionApr 2029 (estimated)
  4. Study completionApr 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
750 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07768488
Sponsor's protocol ID
85231
Other IDs
R01DK142823
Status last verified
Aug 2026
First submitted
12 Aug 2026
Last updated
17 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: We will post study materials (including the Study Protocol, Statistical Analysis Plan, de-identified participant data, and Analytic Code) to a public repository (e.g., GitHub or similar) upon publication of study findings.

Questions about this trial

What is this clinical trial studying?

A study testing Counter-marketing and Health education in people with Social Media and Diet Quality, run by Stanford University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 17 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Amanda Food Policy Lab Study Team (408-598-2672, foodpolicylab@stanford.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Diet quality (Healthy Eating Index-2020 score) (time frame: At 0-months (baseline), 3-months (immediately post- intervention), and 9-months (6-months post-intervention)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Aug 2026.

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