- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07768488
Evaluating Food Messaging Campaigns for Young Adults
14. August 2026 aktualisiert von: 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.
Studienübersicht
Status
Noch keine Rekrutierung
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Interventionell
Einschreibung (Geschätzt)
750
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Amanda Food Policy Lab Study Team
- Telefonnummer: 408-598-2672
- E-Mail: foodpolicylab@stanford.edu
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Ja
Beschreibung
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
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
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).
|
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.
|
|
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.
|
Participants will receive messages about the health consequences of sugary drinks and processed snack foods.
Messages are delivered via Instagram posts.
|
|
Aktiver Komparator: 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.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Diet quality (Healthy Eating Index-2020 score)
Zeitfenster: 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)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Consumption of target food groups
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Hauptermittler: Anna H. Grummon, Stanford School of Medicine
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
1. September 2027
Primärer Abschluss (Geschätzt)
1. April 2029
Studienabschluss (Geschätzt)
1. April 2029
Studienanmeldedaten
Zuerst eingereicht
12. August 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
14. August 2026
Zuerst gepostet (Tatsächlich)
17. August 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
17. August 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
14. August 2026
Zuletzt verifiziert
1. August 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 85231
- R01DK142823 (US NIH Stipendium/Vertrag)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
JA
Beschreibung des IPD-Plans
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-Sharing-Zeitrahmen
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-Sharing-Zugriffskriterien
Anyone will be able to access materials via the public repository.
Art der unterstützenden IPD-Freigabeinformationen
- STUDIENPROTOKOLL
- SAFT
- ANALYTIC_CODE
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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