Evaluating Food Messaging Campaigns for Young Adults
Evaluating a Counter-marketing Campaign to Improve Diet Quality Among Young Adults
Aperçu de l'étude
Statut
Statut
Les conditions
Les conditions
Intervention / Traitement
Intervention / Traitement
Description détaillée
Type d'étude
Type d'étude
Inscription (Estimé)
Inscription
Phase
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
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
Critère d'éligibilité
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
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
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Nombre de bras
Armes et Interventions
Groupe de participants / BrasGroupe de participants / Bras |
Intervention / TraitementIntervention / 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).
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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.
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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.
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Participants will receive messages about the health consequences of sugary drinks and processed snack foods.
Messages are delivered via Instagram posts.
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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.
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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
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
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Diet quality (Healthy Eating Index-2020 score)
Délai: At 0-months (baseline), 3-months (immediately post- intervention), and 9-months (6-months post-intervention)
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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).
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At 0-months (baseline), 3-months (immediately post- intervention), and 9-months (6-months post-intervention)
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Mesures de résultats secondaires
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Consumption of target food groups
Délai: At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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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).
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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.
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At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention).
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Disordered eating attitudes and behaviors
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 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)
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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.
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At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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Externalized weight stigma
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 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.
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At 0-months (baseline), 3-months (immediately post-intervention), and 9-months (6-months post-intervention)
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Collaborateurs et enquêteurs
Parrainer
Parrainer
Collaborateurs
Collaborateurs
Les enquêteurs
Les enquêteurs
- Chercheur principal: Anna H. Grummon, Stanford School of Medicine
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Début de l'étude
Achèvement primaire (Estimé)
Achèvement primaire
Achèvement de l'étude (Estimé)
Achèvement de l'étude
Dates d'inscription aux études
Première soumission
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Première publication
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour publiée
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
Autres numéros d'identification d'étude
- 85231
- R01DK142823 (Subvention/contrat des NIH des États-Unis)
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Délai de partage IPD
Critères d'accès au partage IPD
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
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