Mental Imagery to Increase Face Covering Use in UK-based Public Places During the COVID-19 Pandemic

October 9, 2020 updated by: Dominic Conroy, University of East London
Wearing face coverings in enclosed public spaces is a key public health measure to limit viral spread during the 2020 Covid-19 pandemic. Health psychologists are interested in developing interventions that can increase the likelihood of health-adherent and protective behaviours being consistently undertaken at a general population level. Mental imagery interventions are one way in which behavioural scientists and health psychologists try to encourage behaviour change. Mental imagery involves thinking about, and then writing about, anticipated positive outcomes or key practical requirements of a defined health-related action (e.g. 'moderate alcohol consumption'; 'engaging in regular physical activity'). For this project, the investigators are exploring a mental imagery intervention created to encourage regular and consistent wearing of face coverings in public places where this is currently required in the UK. The investigators will test whether engaging in a mental imagery exercise results in any improvement in wearing a face covering (or intention to wear a face covering) one month later relative to reading a public health message about face coverings. In addition, the investigators will explore belief-based and personality-related factors that might make a difference to the effectiveness of the mental imagery intervention.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

Background The 2020 Covid-19 pandemic has required wide-ranging efforts to minimize the spread of the virus and to protect those most vulnerable to becoming unwell as a result of viral infection. These measures include social distancing, regular hand washing and wearing face coverings in public places where an individual is, inevitably, in closer proximity to non-household others than when not in a public place.

The evidence base for using face coverings in the context of the Covid-19 virus has been mixed and is applied in different ways in different countries. However, there is scientific consensus has been that wearing a face covering is likely to decrease viral transmissibility and, relatedly, substantially reduce the death toll and economic impact of the pandemic. The scientific evidence suggests that face coverings primarily offer protection to other people from the person wearing the face covering (who may, knowingly or not, been infected with the virus) rather than offering the person wearing the face covering personal protection themselves. In the UK, the most recent government advice (at time of writing, published on 7th August 2020) supports the use of face coverings.

Previous studies have suggested that varied demographic and belief-based factors (including perceived benefits) may influence variation in individuals' willingness to wear a face covering in the context of a viral epidemic/pandemic past and present. The Covid-19 pandemic is particular in the sense that the risk of viral infection is understood to be greatest to individuals other than the wearer of the face covering and, for this reason, psychological theories concerned with risk susceptibility/vulnerability (e.g. Protection Motivation Theory; Health Belief Model) may have less predictive utility in the context of the 2020 pandemic. However, other social-cognitive psychological theory may offer valuable insights into factors linked to face covering adherence. For example, variation in face covering wearing adherence would be predicted by traditional behavioural science theory as closely linked to a range of key beliefs about the target behaviour. Relevant belief-related factors include attitudes towards face covering (i.e. whether an individual holds (un)favourable beliefs about face covering are held), subjective norms towards face covering (e.g. whether an individual believes that important others such as friends and family hold (un)favourable beliefs about face covering), and perceived behavioural control towards face covering (i.e. the extent to which an individual believes they possess control over deciding to wear a face covering). Whether an individual believes they possess a high level of skill in using face coverings in required situations (i.e. public places/spaces) would also be theorized to predict face covering behaviour.

A further consideration linked to individual adherence to face covering requirements is what 'type' of person that individual is in terms of various relevant personality traits. For example, a relatively conscientious person might be expected to be more likely to routinely wear a face covering to protect individuals in close proximity from the risk of viral infection. Similarly, face covering adherence might be more likely among individuals whose personalities are characterised by humanistic, beneficent orientations towards other people. By contrast, an individual who self-reports high levels of narcissism, may be less likely to wear a face covering given that wearing a face covering might clash with their relatively vain/egotistical self-image.

In summary, this study aims to determine if different types of mental imagery intervention impact on face covering intentions and face covering adherence at a follow-up time point. The second study aim is to explore, through exploratory analyses, whether individual differences in light triad traits, conscientiousness, and narcissism will influence the impact of imagery interventions. Thirdly, the moderating role of social-cognitive variables of intervention effects will be explored. Fourthly, variation in 'imagery ability' (how capable individuals are at visualizing future actions) will be examined as a mediator of potential intervention effects.

Research questions

  1. Do mental imagery exercises increase intentions to use face coverings in public where required?
  2. Do mental imagery exercises increase self-reported wearing of face coverings in public where required?
  3. Do light triad personality traits moderate the relationship between condition allocation (imagery or not) and self-reported face covering wearing intention or action?
  4. Do Theory of Planned Behaviour variables moderate/mediate the relationship between condition allocation (imagery or not) and self-reported face covering wearing intention or action?
  5. Does imagery ability moderate/mediate the relationship between condition allocation (imagery or not) and self-reported face covering wearing intention or action?

Hypotheses

It is hypothesised that individuals assigned to any imagery intervention condition will report:

  1. Significantly higher intentions to wear face coverings in public places where these are required, relative to the control condition at T2 (primary outcome; hypothesis 1).
  2. Significantly higher levels of self-reported face covering relative to the control condition at T3 (primary outcome; hypothesis 2).
  3. Significantly more favourable attitudes, subjective norms, barrier self-efficacy and perceived behavioural control linked to face covering wearing at T2 and T3 (hypotheses 3 and 4).
  4. Finally, it is hypothesied that imagery intervention effects on primary outcome variables at T2 and T3 will be conditional on being more conscientious, less narcissistic, and being characterised by higher levels of 'light triad' personality traits (hypothesis 5).

Study Type

Interventional

Enrollment (Anticipated)

250

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

      • London, United Kingdom
        • Recruiting
        • University of East London
        • Contact:
          • Dominic Conroy, PhD

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18+ year old adults

Exclusion Criteria:

  • Not currently living in the UK

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Outcome imagery
Outcome imagery condition participants will be asked to visualize themselves successfully wearing a face covering in all required public places/situations over coming week, and to imagine how they would feel. The importance of imagining distinctive relevant visual imagery linked to having successfully routinely worn face covering will be underscored in this passage. Outcome imagery participants will then be asked to write in a free-text box how they would feel having successfully worn a face covering in required public places/situations over the week ahead.
Mental imagery involves the mental representation of a future event, action, or task. By imitating or rehearsing this mental event or series of events" (Taylor et al., 1998, p. 430) mental imagery interventionists theorise that an individual's preparation for, and motivation toward, a future action can be made more likely. Mental imagery involves an individual following a set of pre-defined exercises involving thinking about, visualising and writing about a health-related action. Mental imagery exercises can involve focusing on anticipated positive/beneficial outcomes of an action (outcome imagery) or imagery relating to the anticipated strategies/preparation that would be required to successfully execute a pre-defined action (process imagery).
Experimental: Process imagery
Process imagery condition participants will be asked to visualize the kinds of strategies involved in successfully wearing a face covering in all required public places/situations over the coming week. The importance of imagining distinctive relevant visual imagery linked to having effective strategies involved in successfully wearing a face covering in required public places/situations over the week ahead will be underscored in this passage. Process imagery participants will then be asked to write in a free-text box about the kinds of strategies that would be involved in successfully wearing a face covering in all required public places/situations over the coming week.
Mental imagery involves the mental representation of a future event, action, or task. By imitating or rehearsing this mental event or series of events" (Taylor et al., 1998, p. 430) mental imagery interventionists theorise that an individual's preparation for, and motivation toward, a future action can be made more likely. Mental imagery involves an individual following a set of pre-defined exercises involving thinking about, visualising and writing about a health-related action. Mental imagery exercises can involve focusing on anticipated positive/beneficial outcomes of an action (outcome imagery) or imagery relating to the anticipated strategies/preparation that would be required to successfully execute a pre-defined action (process imagery).
Experimental: Combined imagery (outcome imagery and process imagery)
A third experimental condition will receive both outcome and process imagery exercises to read and complete in sequential order.
Mental imagery involves the mental representation of a future event, action, or task. By imitating or rehearsing this mental event or series of events" (Taylor et al., 1998, p. 430) mental imagery interventionists theorise that an individual's preparation for, and motivation toward, a future action can be made more likely. Mental imagery involves an individual following a set of pre-defined exercises involving thinking about, visualising and writing about a health-related action. Mental imagery exercises can involve focusing on anticipated positive/beneficial outcomes of an action (outcome imagery) or imagery relating to the anticipated strategies/preparation that would be required to successfully execute a pre-defined action (process imagery).
No Intervention: Public health message
A fourth condition will involve viewing a UK Government public health message (HM Government, 2020) circulated on social media as an image concerning the importance of wearing face covering while in public places.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Face covering wearing consistency
Time Frame: 4 weeks post-intervention
Self-reported single item response statement with a Likert-type response. Minimum value = 1; maximum value = 5 (a higher score indicates a better outcome).
4 weeks post-intervention
Face covering wearing intention
Time Frame: 4 weeks post-intervention
Self-reported three item response scale with Likert-type responses. Minimum value = 1; maximum value = 5 (a higher score indicates a better outcome).
4 weeks post-intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Attitude toward wearing a face covering
Time Frame: 4 weeks post-intervention
Self-reported 3 item response scale with Likert-type responses. Minimum value = 1; maximum value = 5 (a higher score indicates a worse outcome).
4 weeks post-intervention
Injunctive norm beliefs about wearing a face covering
Time Frame: 4 weeks post-intervention
Self-reported 2 item response scale with Likert-type responses. Minimum value = 1; maximum value = 5 (a higher score indicates a better outcome).
4 weeks post-intervention
Descriptive norm beliefs about wearing a face covering
Time Frame: 4 weeks post-intervention
Self-reported 2 item response scale with Likert-type responses. Minimum value = 1; maximum value = 5 (a higher score indicates a better outcome).
4 weeks post-intervention
Perceived behavioural control over wearing a face covering
Time Frame: 4 weeks post-intervention
Self-reported 3 item response scale with Likert-type responses. Minimum value = 1; maximum value = 5 (a higher score indicates a better outcome).
4 weeks post-intervention
Barrier self-efficacy to wearing a face covering
Time Frame: 4 weeks post-intervention
Self-reported 6 item response scale with Likert-type responses. Minimum value = 1; maximum value = 5 (a higher score indicates a better outcome).
4 weeks post-intervention

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

August 19, 2020

Primary Completion (Anticipated)

December 1, 2020

Study Completion (Anticipated)

December 1, 2020

Study Registration Dates

First Submitted

October 2, 2020

First Submitted That Met QC Criteria

October 9, 2020

First Posted (Actual)

October 12, 2020

Study Record Updates

Last Update Posted (Actual)

October 12, 2020

Last Update Submitted That Met QC Criteria

October 9, 2020

Last Verified

October 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

We will share the anonymised data as a Supplementary file when submitting a research write-up as an article to a suitable academic journal.

IPD Sharing Time Frame

Data will be made available on completion of article publication. Data will be made permanently available.

IPD Sharing Supporting Information Type

  • Study Protocol

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.

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