Salt Warning Label Restaurant Study

March 27, 2025 updated by: Eric Robinson, University of Liverpool

Perceived Effectiveness of Salt Warning Labels on a UK Restaurant Menu: a Real-world Pilot Experiment

This between-subjects randomised controlled trial aims to test the effect of a menu featuring salt warning labels on perceived message effectiveness relative to a menu with no labels in a real-world restaurant environment. The study will also act as a pilot experiment for examining the impact of the salt warning label on food choice and subsequent salt intake in real-world conditions.

Primary objectives:

  • To measure the PME of a menu featuring salt warning labels relative to a menu with no labels
  • To measure label awareness, perceived knowledge gain, and perceived influence of the label on food choice

Secondary objectives:

  • To identify whether there is an effect of the salt warning label on:

    • Food choice (label/no label)
    • Total salt selected
    • Total salt intake
  • To examine support for the introduction of a salt warning label policy in the UK

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

465

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Merseyside
      • Liverpool, Merseyside, United Kingdom, L69 7ZA
        • University of Liverpool

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Are a UK resident
  • Are aged 18 years and above
  • Are fluent in English
  • Eat an out-of-home meal at least once a month on average
  • Have no dietary allergies
  • Are not vegan

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Label group
Participants will receive a manipulated restaurant menu featuring salt warning labels next to menu items that are high in salt.
A salt warning label will feature on the restaurant menu next to menu items that are high in salt (>3g, more than 50% of guideline daily amount [GDA] in the UK).
No Intervention: Control group (no label)
Participants will receive a standard restaurant menu (no labels).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived message effectiveness (PME)
Time Frame: Post - meal assessment (within 10 minutes)
Participants will answer 3 PME questions using a Likert scale ranging from 1 - 5 anchored by "not at all" and "a great deal": Prompt: "Think back to the menu that you ordered from…" "The menu made me concerned about the health effects of consuming items high in salt", "The menu made consuming items high in salt seem unpleasant", "The menu discouraged me from wanting to consume items high in salt". The mean response to the three items will be calculated.
Post - meal assessment (within 10 minutes)
Label awareness
Time Frame: Post - meal assessment (within 10 minutes)

"Did you notice any warning labels next to any of the menu items when making your meal selection?" (yes/no).

If [yes], "What did the label tell you about?" Response options: Healthy items, Organic, Calcium, Sustainable, Added sugars, Vegetarian, Unhealthy items, Salt, Fibre, Gluten Free, None of these, Not sure.

If [yes], "Please describe what the label said" (open text response). Responses that mention high in salt or similar will be coded as aware.

Post - meal assessment (within 10 minutes)
Salt awareness
Time Frame: Post - meal assessment (within 10 minutes)
"Did you think about the salt content of the meals when making your selection?" (yes/no)
Post - meal assessment (within 10 minutes)
Perceived knowledge gain
Time Frame: Post - meal assessment (within 10 minutes)
For this question, both conditions will be shown an image of the labelled menu. "Did you learn something new from the salt labels on the menu?" (yes/no).
Post - meal assessment (within 10 minutes)
Perceived influence
Time Frame: Post - meal assessment (within 10 minutes)

For this question, both conditions will be shown an image of the labelled menu, and some question phrasing is slightly altered.

"Did the salt label influence which food you ordered from the menu" (yes/no). "If [yes], how did the salt label influence your choice?" Response options: I avoided choosing a meal high in salt; I chose a meal high in salt; Other (free text response) Control: "Would the salt label have influenced what food you ordered from the menu?" (yes/no) If [yes], how would the salt label have influenced your choice? Response options: I would have avoided choosing a meal high in salt; I would have chosen a meal high in salt; Other (free text response)

Post - meal assessment (within 10 minutes)
Policy support
Time Frame: Post - meal assessment (within 10 minutes)

For this question, the both conditions will be shown an image of the labelled menu.

If the UK Government introduced policy requiring restaurant menu items high in salt to feature these labels, how would you feel?" Likert scale ranging from 1 - 5 anchored by "strongly oppose" and "strongly support".

Post - meal assessment (within 10 minutes)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total salt purchased
Time Frame: Post - meal assessment (within 10 minutes)
Determined based on the total order of the participant, including food and drink. Prior to study commencement, all menu items will be sent for nutritional analysis to determine salt content/100g. Menu items will be weighed before being sent for analysis using kitchen scales (Vitafit VT706), so that specific salt content per serving can be calculated.
Post - meal assessment (within 10 minutes)
Labelled item selected
Time Frame: Post - meal assessment (within 10 minutes)
Determined based on whether the food item selected featured a high in salt warning label (yes = 1, no = 0).
Post - meal assessment (within 10 minutes)
Total salt consumed
Time Frame: Post - meal assessment (within 10 minutes)
Salt consumption will be determined from the order that the researcher takes and an estimation of the proportion of the meal that was consumed. The researcher will take a photograph before and after consumption and will estimate the percentage consumed component(s) of the meal, taking into account whether participants leave a proportion of all meal components or specific components (e.g., low salt or high salt components). Participants will also be asked whether they shared any of their meal with someone else. A random 10% selection of percentage estimates will be performed by a second researcher to measure reliability. Food consumption will then be calculated by subtracting an estimation of the proportion of the meal that was consumed (taking into account if any has been shared) from the food purchase.
Post - meal assessment (within 10 minutes)
Later salt intake
Time Frame: Follow-up assessment (next morning, 8AM, to be completed within 24 hours)
Participants will receive a link to a dietary recall questionnaire (Intake24, https://intake24.co.uk/) via email on the same day after taking part in the study, which they will be prompted to complete before bed. They will be asked to provide as much detail as possible on what they had for dinner, snacks, and drinks after the restaurant visit. Based on this information and salt values calculated by Intake24, the total salt consumed by the participants for the rest of the day after the visit will be estimated.
Follow-up assessment (next morning, 8AM, to be completed within 24 hours)
Other macronutrient intake
Time Frame: Post - meal assessment (within 10 minutes)
Total kcal, sugar, and saturated fat intake [i.e., other nutrients that are not the main warning focus] will be calculated based on the nutritional content of the order of the participant.
Post - meal assessment (within 10 minutes)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Food choice motives
Time Frame: Post - meal assessment (within 10 minutes)
The "health" subsection of the Food Choice Questionnaire will be used to measure the extent to which health motives may influence participants' food choices. The subsection consists of 6 items, e.g. "It is important to me that the food I eat on a typical day….is nutritious" answered on a 4-point Likert scale ranging from "Not at all important" to "Very important". The mean response for the six items will be calculated.
Post - meal assessment (within 10 minutes)
Aim guessing
Time Frame: Post - meal assessment (within 10 minutes)
Participants are told that the study is about dining habits in restaurants. At the start of the post-meal assessments, participants will be asked what they think the aims of the study were (free text response). Any participant that guesses the study aims to be investigating the influence of food warning labels on food choice will be coded as being aware of study aims. One researcher will code awareness of aims (R.E.) and a second researcher will independently verify the coding.
Post - meal assessment (within 10 minutes)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 3, 2024

Primary Completion (Actual)

September 14, 2024

Study Completion (Actual)

September 14, 2024

Study Registration Dates

First Submitted

June 3, 2024

First Submitted That Met QC Criteria

June 7, 2024

First Posted (Actual)

June 13, 2024

Study Record Updates

Last Update Posted (Actual)

April 2, 2025

Last Update Submitted That Met QC Criteria

March 27, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • rfj78drdsu52lsbw3kztnbpne8xdao

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The anonymised dataset has been uploaded to the Open Science Framework (OSF) - https://osf.io/whzc8/?view_only=e97eb9ff6812457081d6d693e27bf1bd

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Food Selection

Clinical Trials on Salt warning label

Subscribe