Understanding public attitudes towards healthy eating policies

ISRCTN ISRCTN15915360
DOI https://doi.org/10.1186/ISRCTN15915360
Submission date
10/11/2020
Registration date
16/11/2020
Last edited
18/11/2021
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Nutritional, Metabolic, Endocrine
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English Summary

Background and study aims
Obesity rates are high and rising in the UK, and one route to tackling obesity is by the government implementing healthy eating policies. However, public support for healthy eating policies is low which can be a barrier to implementation. Recent research has suggested that if people receive evidence that a policy is effective, then they are more likely to support that policy, however, the best method of communicating complicated evidence is unclear.

The evidence for this study comes from a recent trial in a worksite cafeteria which shows that two healthy eating policies can reduce energy purchased by 11.5%. The current study aims to test two different methods of improving the communication of evidence. The methods tested will be visualising the evidence into an infographic and converting calorie information into its equivalent amount in a familiar food (analogising).

The aim of this study is to investigate whether visualising and analogising evidence can be more effective and changing people’s beliefs about policy effectiveness.

Who can participate?
Any person who is over the age of 16 and living in England can take part.

What does the study involve?
To take part in the study, participants complete an online survey.

At the start of the survey, participants see information about obesity and about two changes to the food environment that can reduce the number of calories people eat. The changes mentioned are replacing some higher calorie foods with lower calorie foods and reducing the portion sizes of some larger foods.

Participants will be split into five different groups, and each group will see different information:
1. Group 1 only sees written information about the current rates of obesity and a description of the two changes
2. Group 2 also sees written information about the current rates of obesity and a description of the two changes. They also see how effective the two changes were at reducing calorie intake
3. Group 3 also sees the same information as Group 2, however, the information is converted from writing into an infographic
4. Group 4 also sees the same written information as Group 2, however, they also see the effectiveness converted from calories into the equivalent amount of calories in a familiar food product: Mars bars
5. Group 5 also sees the same infographic as Group 3, however, this also contains the Mars bars conversion as in Group 4

After seeing these different forms of evidence, participants from all groups are given the same questionnaire. Participants are asked to rate how effective they think the changes were at reducing calorie intake, whether they support the changes being implemented, and whether the evidence was communicated clearly.

What are the possible benefits and risks of participating?
There are no foreseeable risks in taking part. Similarly, there are no specific benefits to taking part.

Where is the study run from?
The University of Cambridge (UK)

When is the study starting and how long is it expected to run for?
From June 2020 to June 2021

Who is funding the study?
Wellcome Trust (UK)

Who is the main contact?
Dr James Reynolds
j.reynolds4@aston.ac.uk

Study website

Contact information

Dr James Reynolds
Scientific

East Forvie Building
Robinson Way
Cambridge
CB2 0SR
United Kingdom

ORCiD logoORCID ID 0000-0003-1536-1557
Phone +44 (0)1223 762569
Email j.reynolds4@aston.ac.uk
Dr James Reynolds
Public

East Forvie Building
Robinson Way
Cambridge
CB2 0SR
United Kingdom

Phone +44 (0)1223 762569
Email j.reynolds4@aston.ac.uk

Study information

Study designA between-participants randomized online survey experiment
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Internet/virtual
Study typeOther
Participant information sheet ISRCTN15915360_PIS_11Nov20.pdf
Scientific titleVisualising and analogising evidence of policy effectiveness: a population-based survey experiment
Study hypothesis1.Communicating evidence of policy effectiveness increases its perceived effectiveness relative to not communicating evidence
2. Communicating evidence of policy effectiveness by visualising information has a larger impact on perceived effectiveness than presenting the same information using text alone
3. Communicating evidence of policy effectiveness using an analogy to translate the effect size has a larger impact on perceived effectiveness than presenting the same information without an analogy
Ethics approval(s)Approved 29/10/2020, Cambridge Psychology Research Ethics Committee (School of the Biological Sciences, University of Cambridge, 17 Mill Lane, Cambridge CB2 1RX; +44 (0)1223 766894; Cheryl.Torbett@admin.cam.ac.uk), ref: PRE.2020.102
ConditionInappropriate diet and eating habits, excess energy intake, healthy eating policies
InterventionParticipants will be randomised (1:1:1:1:1:1) into 5 different groups using the QuestionPro randomisation feature. All participants will complete an online survey, in which they will be presented with different information depending upon their intervention group.

All five groups will receive the same background information about obesity in the UK and a brief description of two interventions. These interventions are availability (replacing some higher calorie food options with lower calorie food options in cafes and restaurants) and size (reducing the portion size of higher calorie food options in cafes and restaurants).

Four of the five groups will receive further information. Group 1 (the control group) will be provided with no information on intervention effectiveness. Group 2 (the ‘assert and quantify’ group) will be provided with an additional sentence that asserts and quantifies the effectiveness of the two interventions. Group 3 (the ‘assert, quantify and visualise’ group) will be provided with the same information as Group 2, however this information will be integrated into an infographic and presented visually. Group 4 (the ‘assert, quantify and analogise’ group) will be provided with the same information as Group 2, however a further sentence will be added that translates the number of calories information into the equivalent amount food (Mars bars). Group 5 (the ‘assert, quantify, visualise and analogise’ group) will be provided with the same visualised information as Group 3 with the addition of the analogy used in Group 4. The study will be conducted using an online survey platform, called QuestionPro.

Each group will have a single exposure to the intervention and will be able to view and read the information in the intervention for as long as they wish before moving on to the questions. The entire survey including the intervention exposure and questionnaire will last an estimated 5 minutes.
Intervention typeBehavioural
Primary outcome measure1. Perceived effectiveness of availability plus size interventions at reducing calorie intake measured as a composite variable using the mean of two items on a 7-point response scale at a single timepoint
Secondary outcome measures1. Perceived effectiveness of the interventions individually measured as a composite variable using the mean of two items on a 7-point response scale for each intervention at a single timepoint
2. Acceptability of interventions measured using a single item on a 7-point response scale for each intervention individually, and both together, at a single timepoint
3. Subjective comprehension of the interventions measured as a composite variable using the mean of two self-rated items on a 7-point response scale at a single timepoint
4. Recall of the intervention content measured from three possible correct answers from two questions (scored from 0-3) at a single timepoint
Overall study start date25/06/2020
Overall study end date01/06/2021

Eligibility

Participant type(s)All
Age groupAdult
SexBoth
Target number of participantsApproximately 4500 participants will be recruited by a research agency.
Participant inclusion criteria1. Aged ≥16 years
2. Resident in England
Participant exclusion criteriaDoes not meet inclusion criteria.
Recruitment start date06/12/2020
Recruitment end date31/01/2021

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

University of Cambridge
Behaviour Change by Design
East Forvie Building
Robinson Way
Cambridge
CB2 0SR
United Kingdom

Sponsor information

University of Cambridge
University/education

Trinity Lane
Cambridge
CB2 1TN
England
United Kingdom

Phone +44 (0)1223 333543
Email Research_Governance@medschl.cam.ac.uk
Website http://www.cam.ac.uk/
ROR logo "ROR" https://ror.org/013meh722

Funders

Funder type

Research organisation

Wellcome Trust
Private sector organisation / Trusts, charities, foundations (both public and private)
Alternative name(s)
Wellcome, WT
Location
United Kingdom

Results and Publications

Intention to publish date01/05/2021
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryStored in repository
Publication and dissemination planThe results of this research will be written up and submitted to a peer-reviewed, open access journal. The study protocol and statistical analysis plan will be uploaded to https://osf.io.
IPD sharing planThe anonymised datasets, data dictionary, analysis code, materials, and protocol will be stored on multiple online repositorities: The University of Cambridge's repository and https://osf.io. The data will be stored for at least 20 years. Consent from participants for data archiving on these repositories will be obtained in the consent form. There will be no idenfiying information (such as participant IDs, IP addresses, names, or addresses).

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Participant information sheet 11/11/2020 16/11/2020 No Yes

Additional files

ISRCTN15915360_PIS_11Nov20.pdf
Uploaded 16/11/2020

Editorial Notes

18/11/2021: The following changes were made to the trial record:
1. The primary contact email was changed.
2. The plain English summary was updated to reflect these changes.
30/11/2020: Internal review.
16/11/2020: The participant information sheet has been uploaded as an additional file.
13/11/2020: Trial’s existence confirmed by the University of Cambridge.