Perceptions of Weather Risks and Climate Beliefs Among the Hong Kong General Public

May 16, 2022 updated by: Qiuyan Liao, The University of Hong Kong

Climate Change Beliefs, Perceived Risk of Heat Stress and Responses to Heat Health Warnings Among the General Public of Hong Kong: a Mixed-methods Study

Background: Local abnormal heat events may be used as proxies for communicating the health impacts of climate change when people physically feel the effects to reduce the psychological distance of climate change and improve public engagement with climate and weather risk. However, there are concerns that this strategy may be more effective for climate believers, and that it may somewhat compromise the scientific precision because it may lead to erroneous beliefs that climate change is merely characterized by temperature rises or extreme heat but ignore other extreme weather events such as flood and extreme cold, and that cold spells are interpreted as evidence of no climate change. None of these potential effects and concerns has been tested.

Aims: This proposed study is aimed to explore patterns of climate beliefs and their influences on perceptions of heat-related risks and responses to heat health warnings in the general public of Hong Kong; (2) Test the preliminary effects of a revised heat health warning (RHHW) that incorporates information about the health impacts of climate change into existing heat health warning on perceived heat-related risk and climate beliefs.

Design and subjects: This will be a mix-methods study comprising in-depth qualitative interviews, a population-based cohort survey and a pilot randomized control trial (RCT). Subjects will be the general Hong Kong Chinese adults aged ≥18 years.

Main outcome measures: Latent class analysis will be conducted to examine patterns of climate beliefs while structural equation modelling to test the relationships among climate beliefs, perceived heat-related risks and behavioural responses to heat warnings. Qualitative data will be analysed using thematic content analysis while the effect of RHHW will be tested using t-test and linear regression models.

Study Overview

Study Type

Interventional

Enrollment (Actual)

429

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

      • Hong Kong, Hong Kong
        • University of Hong Kong School of Public Health

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

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Participants should own a mobile phone and be able to read Chinese.

Exclusion Criteria:

  • Participants with no mobile phone or cannot understand Chinese will be excluded.

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Participants receive control message
Participants only receive standard heat risk warning
Experimental: Participants receive intervention message
Participants receive standard heat risk warning plus figures incorporating the health impacts of heat and pro-environment behaviors.
Eligible participants will be randomized to either a control condition to receive a standardized heat health warning or an intervention condition to receive a heat health warning plus figures depicting heat risk and pro-environment behavior via their preferred and accessible channel (WhatsApp, WeChat or the text message) each time when a Very Hot Weather Warning is issued by the Hong Kong Observatory.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Emotional engagement with heat and climate change risk (emotional valence)
Time Frame: One week after completion of all messages delivery
Measure participants' emotional engagement with risk of heat stress and climate change, in specific, participants will be asked to indicate how they feel about the health impacts of climate change (using a slider from -3 to 3). Higher scores indicate more positive emotion.
One week after completion of all messages delivery
Emotional engagement with heat and climate change risk (discrete emotion)
Time Frame: One week after completion of all messages delivery
Participants will be asked how much they feel fear/helpless/worried/disgust when thinking about health impacts of climate change (on a 7-point Likert scale). Higher scores indicate stronger emotion arousal.
One week after completion of all messages delivery
Short-term effect of risk perception toward heat and climate change risk
Time Frame: One week after completion of all messages delivery
Their perceived health risk toward climate change and heat stress will be measured using items derived from our baseline and follow-up surveys (likelihood, severity and perceived worry will be used to gauge participants' risk perception). All measures on a 5-point likert scale with higher scores indicating greater risk perception.
One week after completion of all messages delivery
Long-term effect of risk perception toward heat and climate change
Time Frame: One month after completion of all messages delivery
Their perceived health risk toward climate change and heat stress will be measured using items derived from our baseline and follow-up surveys (likelihood, severity and perceived worry will be used to gauge participants' risk perception). All measures on a 5-point likert scale with higher scores indicating greater risk perception.
One month after completion of all messages delivery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short-term effect of self-efficacy in taking pro-environment actions
Time Frame: One week after completion of all messages delivery
Perceived self-efficacy in taking actions to mitigate climate change will be measured by four items derived from previous baseline and follow-up surveys.(Items include: 1) I can personally help to reduce climate change by changing my behavior 2) There are a variety of external factors that make it difficult for me to take actions that help to reduce climate change 3) My action to reduce the effects of climate change in my community will encourage others to reduce the effect of climate change through their own actions 4) If I want, it is easy for me to take actions to help tackle climate change). Responses will be rated on a 5-point Likert (Strongly disagree/Disagree/Agree/Strongly agree/No opinion).
One week after completion of all messages delivery
Long-term effect of self-efficacy in taking pro-environment actions
Time Frame: One month after completion of all messages delivery
Perceived self-efficacy in taking actions to mitigate climate change will be measured by four items derived from previous baseline and follow-up surveys.(Items include: 1) I can personally help to reduce climate change by changing my behavior 2) There are a variety of external factors that make it difficult for me to take actions that help to reduce climate change 3) My action to reduce the effects of climate change in my community will encourage others to reduce the effect of climate change through their own actions 4) If I want, it is easy for me to take actions to help tackle climate change). Responses will be rated on a 5-point Likert (Strongly disagree/Disagree/Agree/Strongly agree/No opinion).
One month after completion of all messages delivery
Short-term effect of intention in taking pro-environment actions
Time Frame: One week after completion of all messages delivery
Participants will also be asked to indicate their intention to 1) reduce energy waste 2) buy energy efficient products, and 3) change some of the daily habits to help tackle climate change. Responses will be rated on a 7-point Likert scale. Higher scores indicate greater behavioral intention.
One week after completion of all messages delivery
Long-term effect of intention in taking pro-environment actions
Time Frame: One month after completion of all messages delivery
Participants will also be asked to indicate their intention to 1) reduce energy waste 2) buy energy efficient products, and 3) change some of the daily habits to help tackle climate change. Responses will be rated on a 7-point Likert scale. Higher scores indicate greater behavioral intention.
One month after completion of all messages delivery

Collaborators and Investigators

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

July 28, 2020

Primary Completion (Actual)

August 30, 2021

Study Completion (Actual)

August 30, 2021

Study Registration Dates

First Submitted

May 28, 2021

First Submitted That Met QC Criteria

June 7, 2021

First Posted (Actual)

June 9, 2021

Study Record Updates

Last Update Posted (Actual)

May 19, 2022

Last Update Submitted That Met QC Criteria

May 16, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • UW 19-093

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Derived data supporting the findings of this study are available from the corresponding author on reasonable request.

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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