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Evaluating Food Messaging Campaigns for Young Adults

perjantai 14. elokuuta 2026 päivittänyt: Anna Grummon, Stanford University

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.

Tutkimuksen yleiskatsaus

Tila

Ei vielä rekrytointia

Ehdot

Interventio / Hoito

Yksityiskohtainen kuvaus

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.

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

750

Vaihe

  • Ei sovellettavissa

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen

Hyväksyy terveitä vapaaehtoisia

Joo

Kuvaus

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:

  • 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

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Ennaltaehkäisy
  • Jako: Satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Yksittäinen

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: 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).
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.
Kokeellinen: 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.
Participants will receive messages about the health consequences of sugary drinks and processed snack foods. Messages are delivered via Instagram posts.
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.
Participants will receive messages describing neutral topic unrelated to food (fire and home safety). Messages are delivered via Instagram posts.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Diet quality (Healthy Eating Index-2020 score)
Aikaikkuna: At 0-months (baseline), 3-months (immediately post- intervention), and 9-months (6-months post-intervention)
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).
At 0-months (baseline), 3-months (immediately post- intervention), and 9-months (6-months post-intervention)

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Consumption of target food groups
Aikaikkuna: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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.
At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
Internalized weight stigma
Aikaikkuna: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention).
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.
At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention).
Disordered eating attitudes and behaviors
Aikaikkuna: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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.
At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
Attitudes toward unhealthy food companies
Aikaikkuna: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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.
At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
Perceived alignment of healthy eating with values
Aikaikkuna: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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.
At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
Externalized weight stigma
Aikaikkuna: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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.
At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
Attribution of individual responsibility for weight
Aikaikkuna: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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.
At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Sponsori

Yhteistyökumppanit

Tutkijat

  • Päätutkija: Anna H. Grummon, Stanford School of Medicine

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

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Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Keskiviikko 12. elokuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Perjantai 14. elokuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Maanantai 17. elokuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Maanantai 17. elokuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Perjantai 14. elokuuta 2026

Viimeksi vahvistettu

Lauantai 1. elokuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muita asiaankuuluvia MeSH-ehtoja

Muut tutkimustunnusnumerot

  • 85231
  • R01DK142823 (Yhdysvaltain NIH-apuraha/sopimus)

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

JOO

IPD-suunnitelman kuvaus

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.

IPD-jaon aikakehys

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.

IPD-jaon käyttöoikeuskriteerit

Anyone will be able to access materials via the public repository.

IPD-jakamista tukeva tietotyyppi

  • STUDY_PROTOCOL
  • MAHLA
  • ANALYTIC_CODE

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .