- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07768488
Evaluating Food Messaging Campaigns for Young Adults
14 août 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Interventionnel
Inscription (Estimé)
750
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Amanda Food Policy Lab Study Team
- Numéro de téléphone: 408-598-2672
- E-mail: foodpolicylab@stanford.edu
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
Oui
La description
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
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: 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.
|
|
Expérimental: 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.
|
|
Comparateur actif: 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.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Diet quality (Healthy Eating Index-2020 score)
Délai: 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)
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Consumption of target food groups
Délai: 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.
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At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
|
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Internalized weight stigma
Délai: 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
Délai: 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.
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At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
|
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Attitudes toward unhealthy food companies
Délai: 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.
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At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
|
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Perceived alignment of healthy eating with values
Délai: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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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
Délai: 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.
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At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
|
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Attribution of individual responsibility for weight
Délai: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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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)
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Anna H. Grummon, Stanford School of Medicine
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 septembre 2027
Achèvement primaire (Estimé)
1 avril 2029
Achèvement de l'étude (Estimé)
1 avril 2029
Dates d'inscription aux études
Première soumission
12 août 2026
Première soumission répondant aux critères de contrôle qualité
14 août 2026
Première publication (Réel)
17 août 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
17 août 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
14 août 2026
Dernière vérification
1 août 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 85231
- R01DK142823 (Subvention/contrat des NIH des États-Unis)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
OUI
Description du régime IPD
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.
Délai de partage IPD
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.
Critères d'accès au partage IPD
Anyone will be able to access materials via the public repository.
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
- ANALYTIC_CODE
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .