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N/A N=63 Prevention

Visual Attention to Text and Pictorial Food Labels: An Eye Tracking Experiment

Health Behavior

Enrolled (actual)
63
Serious AEs
0.0%
Results posted
Aug 2024
Primary outcome: Primary: Amount of Time Spent Looking at the Front-of-package Sodium Label (i.e., Dwell Time) — .96; 1.94; 2.34; 2.58 seconds — p=<0.001

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Text only sodium label (Behavioral); Icon sodium label (Behavioral); Pictorial sodium label (Behavioral); Barcode label (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of North Carolina, Chapel Hill
Primary completion
Sep 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Amount of Time Spent Looking at the Front-of-package Sodium Label (i.e., Dwell Time)
.96; 1.94; 2.34; 2.58 <0.001 sig
SECONDARY
Number of Times Looking at the Front-of-package Sodium Label (i.e., Fixation Count)
5; 9; 11; 13 <.001 sig
SECONDARY
Time to First Fixation on the Front-of-package Sodium Label
.87; .31; .52; .27 .01 sig
SECONDARY
Dwell Time on "Natural" Claim
.90; .91; .87; .74 >.99
SECONDARY
Self-reported Attention to the Front-of-package Sodium Label
2.40; 3.29; 4.16; 4.10 <.001 sig
SECONDARY
Perceived Message Effectiveness of the Front-of-package Sodium Label
1.74; 3.47; 4.13; 3.85 <.001 sig
SECONDARY
Understandability of Front-of-package Sodium Label
3.41; 4.00; 4.22; 4.13 <.001 sig

Summary

The goal of this study is to examine attention elicited by icon, text-only, and control front-of-package food labels. The study also aims to explore whether English language proficiency moderates the impact of icon vs. text-only labels on attention.

Eligibility Criteria

Inclusion Criteria

  • Adult aged 18 or older
  • Self-identifies as Hispanic or Latino

Exclusion Criteria

  • Less than 18 years old
  • Does not identify as Hispanic or Latino
  • Has one of the following conditions: (Wears bifocals, glaucoma, permanently dilated pupils, eye implants [artificial lenses, not contact lenses], less than 2 eyes, or blindness)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05958888). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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