Health Behavior Change During COVID-19 Pandemic

Health Behavior Change During COVID-19 Pandemic: the Focus on Handwashing

This study aims at investigating handwashing behavior during COVID-19 pandemic. It was hypothesized that social-cognitive and emotional predictors as well as COVID-19 morbidity and mortality rates within the country would be associated with handwashing behavior in the general population of adults in 14 countries.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This observational study aims at testing the adherence to handwashing guidelines (the World Health Organization, WHO, 2020) at two measurement points, spanning 1 month. Adults from the general population in 14 countries (Poland, Australia, Canada, China, France, Gambia, Germany, Israel, Italy, Malaysia, Portugal, Romania, Singapore, Switzerland) will provide self-report data on handwashing behavior and its social-cognitive predictors (perceived effectiveness of handwashing, risk perception, outcome expectancy, self-efficacy, intention, planning, and action control), anxiety, as well as COVID-19 morbidity and mortality rates within the country.

Study Type

Observational

Enrollment (Actual)

6079

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

      • Melbourne, Australia
        • The University of Melbourne
      • Fredericton, Canada
        • University of New Brunswick
      • Beijing, China
        • Peking University
      • Bordeaux, France
        • University of Bordeaux
      • Fajara, Gambia
        • London School of Hygiene and Tropical Medicine (in collaboration with MRC Unit The Gambia at LSHTM)
      • Berlin, Germany
        • Freie Universität Berlin
      • Ramat Gan, Israel
        • Bar-Ilan University
      • Padova, Italy
        • University of Padova
      • Serdang, Malaysia
        • Perdana University
    • Lower Silezia
      • Wroclaw, Lower Silezia, Poland, 53-328
        • SWPS University of Social Sciences and Humanities
      • Lisbon, Portugal
        • University of Lisbon
      • Cluj-Napoca, Romania
        • Babes-Bolyai Unversity
      • Singapore, Singapore
        • Nanyang Technological University
      • Zürich, Switzerland
        • University of Zurich

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

Sampling Method

Non-Probability Sample

Study Population

Adults in 14 countries are recruited using the snowballing method. Data are collected using an online platform (software: Qualtricts).

Description

Inclusion Criteria:

  • adults (from general population) who provided informed consent to participate

Exclusion Criteria:

  • younger than <18 years old

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Poland
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Australia
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Canada
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
China
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
France
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Gambia
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Germany
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Israel
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Italy
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Malaysia
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Portugal
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Romania
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Singapore
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country
Switzerland
Adults, general population, N = 400
Observational data collection only, accounting for COVID-19 morbidity and mortality levels within each country

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Handwashing adherence
Time Frame: 1 month
The 12-item self-report measure of adherence to handwashing guidelines across situations (e.g., after visiting public spaces, after touching garbage, etc.) based on the guidelines issued by the World Health Organization and the Centers for Disease Control and Prevention. The responses are provided on a 4-point scale, ranging from 1 (strongly disagree) to 4 (strongly agree). Higher scores indicate better outcomes (the higher level of adherence to handwashing guidelines).
1 month
Frequency of handwashing
Time Frame: 1 month
The 1-item self-report measure of the frequency of handwashing (for at least 20 seconds, all surfaces of the hands) daily. The responses are provided on a 4-point scale, ranging from 1 (less than once) to 5 (more than 10 times). Higher scores indicate better outcomes (the higher frequency of handwashing).
1 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-efficacy
Time Frame: 1 month
4 self-efficacy questionnaire items; mean item score ranging from 1 to 4, higher scores indicate stronger self-efficacy
1 month
Risk perception
Time Frame: 1 month
3 questionnaire items to assess risk perception; mean item score ranging from 1 to 5, higher scores indicate higher risk perception
1 month
Outcome expectancy
Time Frame: 1 month
4 items assessing positive (1 item) and negative (1 items) outcome expectancies; mean item scores ranging from 1 to 4, higher scores indicate more positive outcome expectancies
1 month
Intention
Time Frame: 1 month
2 questionnaire items assessing intention to adhere to handwashing recommendations; mean item scores ranging from 1 to 4, higher scores indicate stronger intention to wash hands (for at least 20 seconds, all surfaces of the hands)
1 month
Planning
Time Frame: 1 month
2 questionnaire items assessing action planning (1 item) and coping planning (1 item); mean item scores ranging from 1 to 4, higher scores indicate a higher level of self-reported planning
1 month
Action control
Time Frame: 1 month
3 questionnaire items assessing a facet of action control, namely self-monitoring; mean item scores ranging from 1 to 4, higher scores indicate a higher level of self-reported monitoring of handwashing behavior
1 month
Perceived effectiveness of hand hygiene
Time Frame: 1 month
1 questionnaire item assessing perceptions of handwashing as an effective means of preventing coronavirus SARS-CoV-2 infection; item scores ranging from 1 to 4, higher scores indicate a higher level of perceived effectiveness of hand hygiene
1 month
Anxiety
Time Frame: 1 month
7-item self-report scale (Generalized Anxiety Disorder, GAD-7) scale to assess anxiety symptoms; mean item scores ranging from 1 to 4, higher scores indicate a higher level of generalized anxiety
1 month
Country-level COVID-19 morbidity and mortality rates
Time Frame: 60 days
The daily cumulative numbers for COVID-19 morbidity and mortality in the study countries. Published daily as the Situation Report by World Health Organization, starting on 21 January 2020. Higher numbers indicate the higher cumulative COVID-19 morbidity and mortality rates in the country.
60 days

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Aleksandra Luszczynska, PhD, SWPS University of Social Sciences and Humanities

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.

General Publications

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)

March 25, 2020

Primary Completion (Actual)

September 24, 2020

Study Completion (Actual)

September 24, 2020

Study Registration Dates

First Submitted

April 28, 2020

First Submitted That Met QC Criteria

April 28, 2020

First Posted (Actual)

April 29, 2020

Study Record Updates

Last Update Posted (Actual)

August 10, 2021

Last Update Submitted That Met QC Criteria

August 8, 2021

Last Verified

August 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

The lead researchers in 14 countries will have full access to data collected across the countries.

In line with the Consortium Agreement (v2, 16th Jul 2020) data will be openly available under following conditions:

De-identified individual participant data that underline the results reported in publications; individual-level aggregated data (e.g., sum scores for scales) used for main analyses in respective publications; available following the publication, no end date of availability; available for analyses that are conducted to achieve aims in the approved proposal.

Due to local regulations, there are exceptions in terms of data sharing rules (stated above):

  • AUSTRALIA: Data from Australia will be available for 5 years after collection.
  • GERMANY, SWITZERLAND: Instead of individual-level sum scores, variance-covariance matrices will be shared.
  • MALAYSIA: Data will not be shared.

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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