- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07768488
Evaluating Food Messaging Campaigns for Young Adults
14 agosto 2026 aggiornato da: 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.
Panoramica dello studio
Stato
Non ancora reclutamento
Condizioni
Descrizione dettagliata
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.
Tipo di studio
Interventistico
Iscrizione (Stimato)
750
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Amanda Food Policy Lab Study Team
- Numero di telefono: 408-598-2672
- Email: foodpolicylab@stanford.edu
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
Accetta volontari sani
Sì
Descrizione
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
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: 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.
|
|
Sperimentale: 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.
|
|
Comparatore attivo: 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.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Diet quality (Healthy Eating Index-2020 score)
Lasso di tempo: 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)
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Consumption of target food groups
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Anna H. Grummon, Stanford School of Medicine
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 settembre 2027
Completamento primario (Stimato)
1 aprile 2029
Completamento dello studio (Stimato)
1 aprile 2029
Date di iscrizione allo studio
Primo inviato
12 agosto 2026
Primo inviato che soddisfa i criteri di controllo qualità
14 agosto 2026
Primo Inserito (Effettivo)
17 agosto 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
17 agosto 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
14 agosto 2026
Ultimo verificato
1 agosto 2026
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 85231
- R01DK142823 (Sovvenzione/contratto NIH degli Stati Uniti)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
SÌ
Descrizione del piano 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.
Periodo di condivisione 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.
Criteri di accesso alla condivisione IPD
Anyone will be able to access materials via the public repository.
Tipo di informazioni di supporto alla condivisione IPD
- STUDIO_PROTOCOLLO
- LINFA
- CODICE_ANALITICO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .