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Designing Impactful Warnings for Sugary Drinks

22 januari 2021 bijgewerkt door: University of North Carolina, Chapel Hill

The goal of this online RCT study is to examine how sugar-sweetened beverage (SSB) health warnings influence US adults' perceptions and reactions. The investigators have the following predictions:

  1. SSB warnings will be perceived as more effective than the control (message topic)
  2. Icon and graphic warnings will be perceived as more effective than text-only warnings (message type)

The investigators will also examine the interaction of warning topic and warning type, but have no specific hypothesis about this interaction.

Finally, the investigators will test the following predictions about the secondary outcomes:

SSB warnings (vs. control), as well as icon and graphic warnings (vs text.warnings), will lead to lower perceived product healthfulness, lower purchase intentions, and higher cognitive elaboration.

Studie Overzicht

Gedetailleerde beschrijving

Childhood obesity is a major public health problem in the US among racial and ethnic minorities, including among the US's growing Latino population. One promising but understudied policy for addressing childhood obesity is requiring warnings on the front of sugar-sweetened beverage containers. However, the topic and design of warnings that are most effective in communicating the harms of sugar-sweetened beverages remains unknown. This study assess which warning topics and which warning designs lead to the greatest perceived message effectiveness among US Latino and non-Latino parents of children ages 2-12. The investigators focus on parents as they are the primary decision-makers and purchasers of food products for children and exert strong influence over their children's dietary intake and food attitudes.

Setting: The trial will take place online on a survey developed using Qualtrics.

Recruitment: Participants will be recruited online by CloudResearch PrimePanels, a survey research platform with access to over 20 million participants. As such, participants will have to be PrimePanels members in order to participate.

Informed Consent: After determining eligibility, eligible participants will be directed to a page on Qualtrics with the consent form. Participants acknowledge their consent in the study by clicking the "next page" arrow and proceeding to the study.

Randomization: After consenting, the participant is randomly assigned to to view one of the 5 warning topics. "WARNING: High in added sugar" (added sugar), "WARNING: Excess consumption of drinks with added sugar contributes to weight gain" (weight gain), "WARNING: Excess consumption of drinks with added sugar contributes to type 2 diabetes" (Type 2 diabetes), "WARNING: Excess consumption of drinks with added sugar contributes to heart damage" (heart damage), and "Please refrain from littering" (control). Within each of the four experimental arms, participants see the message displayed on four different types of warning designs: a text warning on a square background, a text warning on a octagon background, and icon warning, and a graphic warning. Within the control arm, participants see the message displayed on three different types of warning designs: a text warning on a square background, an icon warning, and a graphic warning. Participants randomly see the different warning designs in a random order.

Survey: The participants complete a survey answering behavioral perceptions and intentions questions about the different warning labels.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

1078

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • North Carolina
      • Chapel Hill, North Carolina, Verenigde Staten, 27599
        • University of North Carolina Chapel Hill

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 99 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • at least 18 years old
  • Prime Panels member
  • have at least one child ages 2-12
  • Currently reside in the US

Exclusion Criteria:

  • less than 18 years old

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Preventie
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Added sugar warning message
Message displayed on warning labels is: "WARNING: High in added sugar."
The warning message is in white text on a black square background
The warning message is in white text on a black octagon background
The warning message in in white text on a black background, below an icon that conveys the topic the warning is about
The warning message in in white text on a black background, below a graphic that conveys the topic the warning is about
Experimenteel: Weight gain warning message
Message displayed on warning labels is: "WARNING: Excess consumption of drinks with added sugar contributes to weight gain."
The warning message is in white text on a black square background
The warning message is in white text on a black octagon background
The warning message in in white text on a black background, below an icon that conveys the topic the warning is about
The warning message in in white text on a black background, below a graphic that conveys the topic the warning is about
Experimenteel: Type 2 diabetes warning message
Message displayed on warning labels is: "WARNING: Excess consumption of drinks with added sugar contributes to type 2 diabetes."
The warning message is in white text on a black square background
The warning message is in white text on a black octagon background
The warning message in in white text on a black background, below an icon that conveys the topic the warning is about
The warning message in in white text on a black background, below a graphic that conveys the topic the warning is about
Experimenteel: Heart damage warning message
Message displayed on warning labels is: "WARNING: Excess consumption of drinks with added sugar contributes to heart damage."
The warning message is in white text on a black square background
The warning message is in white text on a black octagon background
The warning message in in white text on a black background, below an icon that conveys the topic the warning is about
The warning message in in white text on a black background, below a graphic that conveys the topic the warning is about
Actieve vergelijker: Neutral message
Message displayed on control label is: "Please refrain from littering."
The warning message is in white text on a black square background
The warning message in in white text on a black background, below an icon that conveys the topic the warning is about
The warning message in in white text on a black background, below a graphic that conveys the topic the warning is about

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Perceived message effectiveness
Tijdsspanne: During survey, which lasts approximately 12-15 minutes.

Perceived message effectiveness as measured by average response to three statements:

This message makes me concerned about the health effects of drinking beverages with added sugar. Response options are on a scale (1=Strongly disagree...5=Strongly agree).

This message makes drinking beverages with added sugar seem unpleasant to me. Response options are on a scale (1=Strongly disagree...5=Strongly agree).

This message discourages me from wanting to drink beverages with added sugar. Response options are on a scale (1=Strongly disagree...5=Strongly agree).

During survey, which lasts approximately 12-15 minutes.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Perceived product healthfulness of beverages with added sugar
Tijdsspanne: During survey, which lasts approximately 12-15 minutes.
Measured with the question, "How healthy or unhealthy would it be for your child to drink beverages with added sugar every day?" Response options are on a scale (1= Very unhealthy...5=Very healthy).
During survey, which lasts approximately 12-15 minutes.
Intentions to purchase beverages with added sugar
Tijdsspanne: During survey, which lasts approximately 12-15 minutes.
Measured with the question, "How likely are you to buy beverages with added sugar for your child in the next four weeks?" Response options are on a scale (1 = Not at all likely...5 = Extremely likely).
During survey, which lasts approximately 12-15 minutes.
Thinking about the health problems from beverages with added sugar
Tijdsspanne: During survey, which lasts approximately 12-15 minutes.
Measured with the question, "How much does this message make you think about the health problems caused by drinking beverages with added sugar?" Response options are on a scale (1=Not at all...5=Very much).
During survey, which lasts approximately 12-15 minutes.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Marissa G Hall, PhD, University of North Carolina

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

7 oktober 2019

Primaire voltooiing (Werkelijk)

4 november 2019

Studie voltooiing (Werkelijk)

4 november 2019

Studieregistratiedata

Eerst ingediend

6 mei 2020

Eerst ingediend dat voldeed aan de QC-criteria

6 mei 2020

Eerst geplaatst (Werkelijk)

11 mei 2020

Updates van studierecords

Laatste update geplaatst (Werkelijk)

25 januari 2021

Laatste update ingediend die voldeed aan QC-criteria

22 januari 2021

Laatst geverifieerd

1 januari 2021

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • 19-0277a

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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