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Impact of Front-of-package Labels on Weight Bias Among Latines

University of North Carolina (UNC) logo

University of North Carolina (UNC)

Status

Completed

Conditions

Weight Prejudice

Treatments

Behavioral: Separated interpretive magnifying glass icon label
Behavioral: Interpretive text-only label
Behavioral: Numerical label
Behavioral: Interpretive magnifying glass icon label

Study type

Interventional

Funder types

Other

Identifiers

NCT06293937
24-0300b

Details and patient eligibility

About

The goal of this experiment is to examine the effects on explicit weight bias of a selection task using 4 different types of front-of-package food labels to select healthy or unhealthy foods among a sample of Latine and low English proficiency adults. The main questions this experiment aims to answer are:

  • Does the use of different front-of-package label designs in a selection task lead to different effects on explicit weight bias among Latine and low English proficiency consumers?
  • Does the use of different front-of-package label designs in a selection task lead to different effects on attribution of personal responsibility for body weight among Latine and low English proficiency consumers?

Participants will be randomly assigned to 1 of 4 types of front-of-package label designs. They will view 3 sets of products (frozen meals, frozen pizzas, and frozen desserts), shown in random order. For each product set, participants will view 3 products shown in random arrangement, each with participants' randomly assigned label shown on the front of package. After viewing all 3 product types, participants will answer questions about explicit weight bias and attribution of responsibility for body weight. Researchers will compare results across label designs.

Full description

This study aims to determine if the use of different front-of-package label types in a selection task leads to different effects on explicit weight bias and attribution of responsibility for body weight among Latine and low English proficiency (LEP) consumers. A Latine-focused panel company will recruit 4,000 US Latine adults of parental age (18-55 years), approximately 50% of whom will have low English proficiency (LEP). In a between-subjects experiment, researchers will randomize participants to 1 of 4 types of front-of-package labels: a numerical label, an interpretive text-only label, an interpretive label with a magnifying glass icon, or separated interpretive labels with a magnifying glass icon. Participants will first perform a selection task for a parent study in which they will view their assigned label on 3 sets of products (with 3 products per set) and select the product they believe is most and least healthy and the product they most want to purchase. After this selection task, participants will answer questions measuring this study's outcomes: explicit weight bias (primary outcome) and attribution of personal responsibility of body weight (secondary outcome).

Enrollment

3,306 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Identifying as Latine or Hispanic
  • Ages 18-55 years old
  • Residing in the United States

Exclusion criteria

  • Not identifying as Latine or Hispanic
  • Less than 18 or greater than 55 years old
  • Not residing in the United States

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

3,306 participants in 4 patient groups

Numerical label
Experimental group
Treatment:
Behavioral: Numerical label
Interpretive text-only label
Experimental group
Treatment:
Behavioral: Interpretive text-only label
Interpretive magnifying glass icon label
Experimental group
Treatment:
Behavioral: Interpretive magnifying glass icon label
Separated interpretive magnifying glass icon label
Experimental group
Treatment:
Behavioral: Separated interpretive magnifying glass icon label

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Aline D'Angelo Campos, MPP

Data sourced from clinicaltrials.gov

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