Evaluating Food Messaging Campaigns for Young Adults
Evaluating a Counter-marketing Campaign to Improve Diet Quality Among Young Adults
Studieoversikt
Status
Status
Forhold
Forhold
Intervensjon / Behandling
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Studietype
Registrering (Antatt)
Registrering
Fase
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
Studiekontakt
- Navn: Amanda Food Policy Lab Study Team
- Telefonnummer: 408-598-2672
- E-post: foodpolicylab@stanford.edu
Deltakelseskriterier
Kvalifikasjonskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Beskrivelse
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
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Antall våpen
Våpen og intervensjoner
Deltakergruppe / ArmDeltakergruppe / Arm |
Intervensjon / BehandlingIntervensjon / Behandling |
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Eksperimentell: 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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Eksperimentell: 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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Aktiv 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.
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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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Hva måler studien?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Diet quality (Healthy Eating Index-2020 score)
Tidsramme: 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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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Consumption of target food groups
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Samarbeidspartnere og etterforskere
Sponsor
Sponsor
Samarbeidspartnere
Samarbeidspartnere
Etterforskere
Etterforskere
- Hovedetterforsker: Anna H. Grummon, Stanford School of Medicine
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Studiestart
Primær fullføring (Antatt)
Primær fullføring
Studiet fullført (Antatt)
Studiet fullført
Datoer for studieregistrering
Først innsendt
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Først lagt ut
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Sist oppdatering lagt ut
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
Andre studie-ID-numre
- 85231
- R01DK142823 (U.S. NIH-stipend/kontrakt)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
Tilgangskriterier for IPD-deling
IPD-deling Støtteinformasjonstype
- STUDY_PROTOCOL
- SEVJE
- ANALYTIC_CODE
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