CClinicalTrials.gg
Not yet recruitingNCT07809295Updated Sep 9, 2026

Food Menu Labelling Effects on Individuals With Eating Disorders and Other Mental Health Conditions.

An interventional study of Control condition and Calorie labelling in Food Labelling, Eating Behaviour and Mental Health, sponsored by University of Liverpool. Not yet recruiting at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-09.

Sponsored by University of Liverpool · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
900
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Calorie labelling in out-of-home (OOH) settings was introduced by the government in England as part of a wider strategy to 'tackle obesity' (DHSC, 2020). The OOH sector encompasses outlets where food and drinks are prepared for immediate consumption, on or off the premises (DHSC, 2021). Increased consumption of OOH food is associated with greater intake of energy and nutrients of concern; therefore, is implicated in poorer dietary quality and ill-health (Gesteiro et al., 2022). The key ambition for the calorie labelling policy was to inform consumers of the calorie content of their food choices, making it easier to select healthier food choices (DHSC, 2020). An additional potential benefit of the policy was to prompt reformulation by the food industry to either reduce the calorie content of foods on offer or provide new lower calorie options (DHSC, 2021).

The calorie labelling policy in England was criticised at the time of implementation in the media for its potential to cause harm in individuals with eating disorders (Polden et al., 2023). However, limited research had explored effects on individuals with eating disorders (Robinson et al., 2023). It is estimated that over a million individuals in the UK are living with an eating disorder (Beat Eating disorders, 2026). Therefore, it is important for research to understand the impact of food labelling interventions on mental health outcomes in individuals with eating disorders and other mental health conditions, and whether alternative nutritional labelling practices that are not focused on calories alone could have positive health impacts without unintended negative consequences.

One alternative form of nutritional labelling that could be considered in OOH settings is Nutri-score. Nutri-score provides food items with a label from A (dark green, healthiest) to E (Red, least healthy) according to the content of both positive (e.g. fibre, protein) and negative (e.g. saturated fat, salt, sugar) nutrients. Nutri-score has been implemented as a front-of-pack label in several countries across Europe, with positive impacts on the healthiness of food purchasing in supermarkets (Andreani et al., 2025). Two studies have assessed Nutri-score in OOH settings, also finding associations between Nutri-score and healthier food choices (Chandon \& Indaburu, 2026; Julia et al., 2021). However, Nutri-score on food menus has not previously been examined in terms of the potential impact on individuals with eating disorders and other mental health outcomes.

Nutri-score encompasses the nutritional quality of a food product, by accounting for both positive and negative components. This may be less harmful to individuals with eating disorders as it would remove the focus on calorie content. Previous qualitative research has shown that individuals with eating disorders may support labelling strategies that provide more holistic approaches to nutrition (Trompeter et al., 2026). It could also be of benefit to general population health to focus on helping individuals to consume a well-rounded diet higher in positive nutrients (fibre, protein), with high fruit, vegetable and nut content, and lower in negative nutrients that contribute to ill health (salt, sugar, fats). To date, limited research has compared Calorie labelling to Nutri-score in the general population or among those living with mental health conditions, like eating disorders.

OBJECTIVES This new study will explore the impact of Nutri-score labelling vs Calorie labelling vs no labelling (Control) in a simulated OOH food delivery ordering platform (common setting for food purchasing and calorie labelling is required by law in England) on participants' perceived effectiveness of nutritional labelling, healthiness of food choices, positive and negative affect, and perceived impacts on mental health.

We will examine effects in a general population sample (no eating disorder diagnosis), a sample of participants with a past or current diagnosis of an eating disorder by a medical practitioner and a sample of participants with a common mental health condition diagnosed by a medical practitioner without eating disorder (e.g., anxiety), in order to understand potential effects across groups of participants who may differ in their risk of poorer mental health in response to nutritional labelling.

(references in attached protocol)

Read the detailed description

See attached study protocol for detailed information

02

Conditions studied

  • Food Labelling
  • Eating Behaviour
  • Mental Health
  • Eating Disorder

Keywords

  • Obesity
  • Food policy
  • Nutritional labelling
  • Food choice
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

  • Residing in the UK
  • Regularly eat food prepared out of the home (from restaurants, cafes, fast food etc., at least once a month)
  • Over the age of 18 years
  • Fluent English speaker
  • Can complete the study on a laptop or desktop computer (not touch screen)
  • Inclusion for specific participant groups:

    1. Current or previous eating disorder diagnosis by a medical practitioner
    2. Current or previous common mental health condition (i.e. anxiety and/or depression) diagnosis by a medical practitioner but no eating disorder diagnosis
    3. No diagnosis of eating disorder or mental health condition

Exclusion Criteria:

  • Pregnant/breastfeeding
  • Have taken part in a previous study using the same version of the online food choice task (exclusion list obtained from prolific)
04

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
900 participants (estimated)

Study arms

  • Other
    Control group

    Participants with no diagnosis of a mental health or eating disorder

    Behavioral: Control condition · Behavioral: Calorie labelling · Behavioral: Nutri-Score labelling

  • Experimental
    Mental health diagnosis group

    Participants with a diagnosis of a mental health condition but no diagnosis of an eating disorder

    Behavioral: Control condition · Behavioral: Calorie labelling · Behavioral: Nutri-Score labelling

  • Experimental
    Eating disorder diagnosis group

    Participants with a diagnosis of an eating disorder

    Behavioral: Control condition · Behavioral: Calorie labelling · Behavioral: Nutri-Score labelling

Interventions

  • BehavioralControl condition

    Participants will be asked to select a meal from a food menu with no nutritional labelling

  • BehavioralCalorie labelling

    Participants will be asked to select a meal from a food menu with calorie labelling

  • BehavioralNutri-Score labelling

    Participants will be asked to select a meal from a food menu with calorie labelling

05

What researchers measure

Primary outcomes

  1. Perceived Message Effectiveness

    An adapted version of the University of North Carolina Perceived Message Effectiveness (PME) scale will be used as a measurement of how effective participants believe nutritional labelling is in promoting behaviour change. The scale measures health concern, product attitude, and discouragement of item consumption in response to public health messaging or in this context, the food menu presented during the study. Participants will be shown a screenshot of the menu they ordered. All participants will answer 3 questions using a Likert scale ranging from 1 - 5 anchored by "Strongly disagree" and "Strongly agree". The mean response to the three items will be calculated. PME is used as an early indicator of a health messages potential to change behaviour (e.g., reduce selection of less healthy items). The scale has been used previously to identify the potential impact of food labels and is predictive of long-term behaviour.

    Time frame: Day 1 of 1: the PME measure will be completed immediately after participants have made their food selection

  2. Perceived usefulness of menu in identifying healthier/less healthy food choices

    Participants will be asked 'To what extent was the menu useful in helping you identify healthy vs. less healthy food choices'. Participants will select their answer on a Likert scale ranging from 1 - 5 anchored by "Strongly disagree" and "Strongly agree".

    Time frame: Day 1 of 1: Participants will rate the perceived usefulness of the menu immediately after making their food selection.

  3. Nutritional quality of food ordered

    An overall measure of nutritional quality of participants food order will be calculated using mean UK NPM scores of individual items, weighted according to the energy content of the item. Nutritional content used to calculate NPM scores for each menu item was obtained from outlet websites and input into the online NPM calculation tool (2004/05). Weighted scores will be calculated using the weighted.mean function in R.

    Time frame: Day 1 of 1: Food orders (item names, energy content, UK Nutrient Profiling Model scores) will be recorded immediately after the baseline questionnaire. The recorded information will be used to calculate weighted NPM scores.]

  4. Positive/negative affect

    Participants will complete an adapted version of PANAS after completing the food selection task. This is a 20-item measure, whereby participants will be asked to 'indicate the extent you feel this way right now' on a scale of 1 to 5 from 'very slightly or not at all' to 'extremely'. Participants receive a positive affect score and a negative affect score.

    Time frame: Day 1 of 1: Participants will complete the PANAS measure immediately after making their food selection

  5. Perceived impact of labelling on mental health

    Questions were developed based on self-reported mental health-related outcomes in previous research. Participants will be asked to respond to each of the following points on a scale of 1 to 5 from 'very slightly or not at all' to 'extremely'. The information on the menus made me feel... * Anxious about my food choice * Guilty about my food choice * Reassured about my food choice * Ashamed about my food choice * Fixated on the nutritional content of my food choice

    Time frame: Day 1 of 1: Participants will complete these measures immediately after making their food choices.

  6. Perceived impact of labelling on mental health

    Two additional questions relating to compensation were adapted from an existing scale related to compensatory eating behaviour and alcohol (CEBRACS). Participants will be asked to respond to each of the following points on a scale of 1 to 5 from 'very slightly or not at all' to 'extremely'. * Like I should eat less than usual during one or more meals to make up for the amount of food I have selected * Like I should skip one or more meals to make up for the amount of food I have selected

    Time frame: Day 1 of 1: Participants will complete this measure immediately after making their food choices

Secondary outcomes

  1. Nutri-Score labels of selected food items

    We will record the Nutri-Score values (A-E) of all items selected by participants in the food choice task. Participants will be coded as having ordered any of the healthiest menu items labelled A or B (Y/N) and/or the least healthy menu items labelled D or E (Y/N).

    Time frame: Day 1 of 1: UK Nutrient Profiling Model scores of food orders will be recorded immediately after the baseline questionnaire.

  2. Energy content of meals

    We will record the energy and nutrient content of all items selected by participants in the food choice task. The total energy content of the ordered meal will be calculated.

    Time frame: Day 1 of 1: energy content of food orders will be recorded immediately after the baseline questionnaire.

Other outcomes

  1. Participant education

    Participants will be asked to report their highest level of education achieved: * Less than high school * High school completion * College or foundation degree * Bachelor's degree * Master's degree

    Time frame: Day 1 of 1: Participants will report demographic data in a baseline questionnaire prior to completing the food selection task Participants will be asked this question in the follow-up survey as an consistency check after the food selection task

  2. Notice and impact of labels

    Participants will be asked several questions to assess whether they noticed any nutritional labelling, and if the labelling impacted their food choices. Questions will be amended slightly according to labelling condition.

    Time frame: Day 1 of 1: Participants will be asked these questions immediately after the food selection task

  3. Participant age

    Participants will report their age on a dropdown list

    Time frame: Day 1 of 1: Participants will report demographic data in a baseline questionnaire prior to completing the food selection task

  4. Participant gender

    Participants will select their gender from the following options: * Man * Woman * Non-binary * Other * Prefer not to say

    Time frame: Day 1 of 1: Participants will report demographic data in a baseline questionnaire prior to completing the food selection task

  5. Participant ethnicity

    Participants will select their ethnicity from a dropdown list: White English/Welsh/Scottish/Northern Irish/British White Irish Any other White background White and Black Caribbean White and Black African Any other mixed/multiple ethnic background please describe Indian Pakistani Bangladeshi Chinese Other Asian African Caribbean Arab Any other ethnic group

    Time frame: Day 1 of 1: Participants will report demographic data in a baseline questionnaire prior to completing the food selection task

  6. Participant height

    Participants will report their height in either cm or ft and inches. This will be converted to metres in order to calculate BMI.

    Time frame: Day 1 of 1: Participants will be asked these questions immediately after the food selection task

  7. Participant weight

    Participants will report their weight in either kg or stones and pounds. All will be converted if necessary to KG to calculate BMI.

    Time frame: Day 1 of 1: Participants will be asked these questions immediately after the food selection task

  8. Frequency of consumption of OOH food

    Participants will be asked how often over the past year they have eaten food prepared out of the home (from restaurants, cafes, fast food etc.). The following options will be listed. * Not in the last year * Less than once per month * 1-3 times per month * 1-2 times per week * 3 times per week or more

    Time frame: Day 1 of 1: Participants will report this in a baseline questionnaire prior to completing the food selection task

06

Study locations

1 site
  • University of Liverpool
    Liverpool, Merseyside L69 7ZA, United Kingdom
07

References and documents

Individual participant data

Plan to share: Yes — Anonymised participant data will be placed in an online data repository for other researchers to use in the future.

Supporting information: Study protocol, Sap, Icf, Analytic code

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07809295
Lead sponsor
University of Liverpool
Collaborators
King's College London, University of Oxford, Liverpool John Moores University
Responsible party
Sponsor
First posted
Sep 9, 2026
Start date
Sep 2026 (estimated)
Primary completion
Sep 2026 (estimated)
Completion
Sep 2026 (estimated)
Last update
Sep 9, 2026

Study contacts

Eric Robinson, PhD
Contact
robinsoe@liverpool.ac.uk
+44 151794 ext. 1187
Amy Finlay, PhD
Contact
amy.finlay@liverpool.ac.uk
Eric Robinson, PhD
principal investigator · University of Liverpool

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion