Food Choice Among Individuals With an Eating Disorder Diagnosis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Liverpool

About this trial

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.

Eligibility criteria

Qualifiers

Current or past eating disorder diagnosis

Aged 18+

Live in the UK

Fluent English speaker

Disqualifiers

Currently partaking in a fast or any other restrictive eating

Any dietary restrictions/intolerances (eg. Vegan, Gluten-free, etc.)

Trial design

Treatments tested in this trial

  • Front-of-pack nutrition labelling

Treatment groups

246 Participants
are divided into 3 treatment groups

Sponsors and collaborators

University of Liverpool

Lead sponsor

National Institute for Health Research, United Kingdom

Collaborator