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Study identifier: NCT07339969 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Food Choice Among Individuals With an Eating Disorder Diagnosis

Condition: Eating Behavior Disorders  ·  Sponsor: University of Liverpool

PhaseNA
Planned participants246
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The aim of this study is to understand the impact of front of pack labelling systems such as, warning labels and traffic light labels on food choice and negative emotional response in an eating disorder(s) population group. Participants will be recruited to take part in an online study where they will be required to make hypothetical food choices. Participants will complete a baseline no label task, before being randomly assigned to (1) warning label group, (2) traffic light label group, or (3) no label group in which they will complete the same task a second time (mixed design). Each participant, irrespective of the group will be asked to complete five trials within the main task. Participants will view a selection of six packaged food items for scenarios involving labels predominately relating to (1) sugar, (2) salt, (3) fat, (4) saturated fat, and (5) calorie content of the food products. Three items will be 'high in' that particular nutrient and three items will not be high in that nutrient. Participants will be shown all six options at once and will be asked to choose one item. In total, participants will choose five different items, one from each trial. After participants have made their food choices for the second task, they will be asked questions about the task they have just completed.

This description comes directly from the study's public registry record.

Talk to the study team

Rebecca Evans, PhD  ·  0151 794 9832  ·  r.k.evans@liverpool.ac.uk

Rebecca Latham, MSc  ·  0151 794 9832  ·  Rebecca.Latham@liverpool.ac.uk

Always discuss trial participation with your own doctor first.

Locations (1)

University of LiverpoolLiverpool, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT07339969