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Not yet recruitingNCT07768488Updated Aug 17, 2026

Evaluating Food Messaging Campaigns for Young Adults

An interventional study of Counter-marketing and Health education in Social Media, Diet Quality and Diet Intervention, sponsored by Stanford University. Not yet recruiting. Open to participants aged 18 Years to 29 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-17.

Sponsored by Stanford University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
750
Allocation
Randomized
Ages
18 Years to 29 Years
Sex
All
01

Study 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 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.

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Conditions studied

  • Social Media
  • Diet Quality
  • Diet Intervention
  • Communication
  • Young Adults
  • Nutrition

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03

Who can participate

Ages eligible
18 Years to 29 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • 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
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
750 participants (estimated)

Study arms

  • Experimental
    Counter-marketing messages

    Participants 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).

    Behavioral: Counter-marketing

  • Experimental
    Health education messages

    Participants 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.

    Behavioral: Health education

  • Active comparator
    Control (neutral) messages

    Participants 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.

    Behavioral: Control (neutral) messages

Interventions

  • BehavioralCounter-marketing

    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.

  • BehavioralHealth education

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

  • BehavioralControl (neutral) messages

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

05

What researchers measure

Primary outcomes

  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).

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

Secondary outcomes

  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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

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

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: 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.

Supporting information: Study protocol, Sap, Analytic code

No publications or documents are linked to this record.

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Registry details

Key details

Study ID
NCT07768488
Lead sponsor
Stanford University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Responsible party
Anna Grummon (Assistant Professor, Stanford University) — Principal investigator
First posted
Aug 17, 2026
Start date
Sep 2027 (estimated)
Primary completion
Apr 2029 (estimated)
Completion
Apr 2029 (estimated)
Last update
Aug 17, 2026

Study contacts

Amanda Food Policy Lab Study Team
Contact
foodpolicylab@stanford.edu
408-598-2672
Anna H. Grummon
principal investigator · Stanford School of Medicine

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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