The Optimising Isolation, Quarantine and Distancing Study for COVID-19 (Optimise)

The Australian government swift interventions and actions early to the COVID 19 epidemic included enforced quarantine, isolation, varying degrees of social and physical distancing measures, travel restrictions, community level testing and enhanced contact tracing models which effected the trajectory of the epidemic impact. While the search for effective therapeutics and vaccines continues, it is important to understand how to effectively implement and optimise the current public health interventions available; application of traditional contact tracing , contributions of new contact tracing mobile phone applications, community level testing and use of specific fit for purpose diagnostic tests; to screen, detect and provide evidence of infection clearance.

While the suppression measures have been effective on disease transmission rates, it has had economic, social and non COVID-19 health costs impacts. As community restrictions change it will be important to monitor and evaluate the effectiveness of these key interventions. This is a longitudinal study that will follow the experience and behaviors of 2 key risk populations impacted by COVID-19 transmission containment measures.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

This is a mixed methods longitudinal study of a cohort of 1000 participants for a 18 month period. Victorian adults from three key risk populations will be recruited into two longitudinal cohort groups. It will follow the experiences and behaviors of the groups; Recruitment group 1/Seed set 1 - recently diagnosed 'COVID-19 cases' (Group 1) and their social network with up to 2 waves of /Key people, will be followed up for 1 month initially with specific monitoring tools before they will transition into ongoing follow up and monitoring as recruitment group 2 Recruitment group 2/Seed set 2 - people from the general community that are not currently infected with COVID19 'Group 2' that are practicing physical distancing and represent specific key risk groups, and their social network with up to 2 waves of Key people.

Over sampling of vulnerable populations including people with disabilities, single parents and people living alone will be conducted across all groups. Individuals may be invited to participate in more than one cohort when they change between risk population definitions.

The project aims to meet the following objectives using a longitudinal cohort design and a mixed method of qualitative and quantitative tools to enable us to assess changes within individuals over time and to assess the influence of social networks on their health, well-being, attitudes and perceptions.

Objectives of the study are:

  1. To assess adherence to government intervention strategies (i.e. early testing, isolation and physical distancing) and identify factors that promote/inhibit compliance to intervention strategies designed to reduce transmission.
  2. To better understand, assess and monitor the unintended health, social and economic consequences of the government interventions to control COVID-19 transmission
  3. To collect and collate empirical data regarding transmissions dynamics, social contacts and mixing patterns of COVID19 cases , their contacts and key vulnerable groups to develop and refine mathematical models that will improve the precision and timeliness of dynamic transmission estimates.

Study Type

Observational

Enrollment (Estimated)

1000

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

    • Victoria
      • Melbourne, Victoria, Australia, 3004
        • The Macfarlane Burnet Institute for Medical Research and 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

Sampling Method

Probability Sample

Study Population

Volunteer participants over the age of 18 years in Victoria, Australia

Description

Inclusion Criteria:

  • Community participants

Exclusion Criteria:

  • Unable to provide consent

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
Group 1/Seed set 1 - recently diagnosed 'COVID-19 cases
(Group1) and their social network with up to 2 waves of /Key people, will be followed up for 1 month initially with specific monitoring tools before they will transition into ongoing follow up and monitoring as recruitment group 2
Group 2/Seed set 2 - people from the general community that are not currently infected with COVID19
'Group 2' that are practicing physical distancing and represent specific key risk groups, and their social network with up to 2 waves of Key people

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from response in baseline questionnaires to Adherence (non-adherence) with COVID19 transmission containment measures
Time Frame: 18 months
Participants will complete questionnaires and diaries as binary daily measure of outcomes of compliance/nonadherence for each individual, determined by their ability to adhere to government regulations
18 months
Change from response in baseline questionnaires depicting what are the unintended health, social and economic consequences of the government response to control COVID19 transmission
Time Frame: 18 months

Using data from baseline and follow up questionnaires the researchers will calculate both an individual and a composite variable to assess the following unintended consequence, including:

  • Loss of job during COVID-19 period
  • Decline in income during COVID-19 period
  • Disruption to schooling or education during COVID-19 period
  • Decline in work productivity during COVID-19 period
  • Change in responsibilities to care for others
  • Decrease in healthcare utilization during COVID-19 period
  • Increase in alcohol (frequency or quantity) and other drug consumption during COVID-19 period
  • Change in mental health or personal wellbeing during COVID-19 period
  • Increase in social connectedness during COVID-19 period A scale is not being applied in above responses; options for response are in place.
  • Anxiety (using GAD scale: https://patient.info/doctor/generalised-anxiety-disorderassessment-gad-7) is a response section in the questionnaire.
18 months
What are the social contacts and mixing patterns of COVID-19 cases
Time Frame: 18 months

The questionnaire participants will be ask to complete include nominating the number of contacts per day and the time will permit collation of social network data.

Using data from the daily diaries (retrospective and prospective) the researchers will calculate:

  • Numbers of contacts per day
  • Numbers of contacts by type of activity
  • Time spent doing each type of activity per day
  • Time from symptom onset to self-isolation
  • Time from symptom onset to accessing diagnostic testing
  • Time from accessing testing to result receipt (diagnosis)
  • Time from result receipt (diagnosis) - to contact by contact tracing team A scale is not being used.
18 months
What are the types of social contacts and mixing patterns of COVID-19 cases
Time Frame: 18 months
The questionnaire participants will be ask to complete will include nominating the relationship with their contacts per day(i.e. partner, child, friend), and individuals COVID test status, providing detailed specifics of the projects social network data
18 months
Measure of the efficacy of government interventions
Time Frame: 18 months

Participants responses to questionnaires, focus group discussions will be used as binary measurers; The researchers will not be using a scale, reporting will be in the format:

  • Number and % of participants that reported correct knowledge of government guidance regarding isolation, quarantine and physical distancing requirements - calculated as a binary outcome (Yes/No) and also as a combined knowledge score
  • Number and % of participants that report using COVID-19 prevention measures advised by the Governments. For example:
  • 560/700 (80%) participants report regularly using hand sanitizer and/or washing hands
  • 680/700 (97%) of participants report applying physical distancing rules as much as I can (i.e. keeping 1.5 metres away from others, not shaking hands)
  • Number and % of participants that reported COVID-19 related symptoms that were tested for SARS-CoV-2 infection, and results of these tests
18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Collect and collate empirical data of COVID19 cases, contacts and key vulnerable groups
Time Frame: 18 months

The researchers will integrate data from adherence outcomes, social contacts and transmission outcomes from diaries and questioners into key analyses; cross sectional social network models, structural equation modelling & social network analyses.

Researchers will use empirical data regarding transmission dynamics, social contacts and mixing patterns of COVID19 cases, their contacts and key vulnerable groups to develop and refine mathematical models to improve precision and timeliness of dynamic transmission estimate.

The researchers will use social contacts and transmission outcomes to update deterministic compartmental epidemic model to estimate the effect of testing and surveillance on the spread of COVID-19 in Australia.

18 months
Assess the effectiveness of government interventions to reduce COVID-19 transmission from questionnaire responses from cohort participants
Time Frame: 18 months

Including but not limited to the number/proportion of participants with accurate knowledge of government recommendations and the number/proportion of participants using COVID-19 prevention measures as recommended. The researchers will analyse adherence outcomes using serial cross-sectional approach to estimate a adherence level for participant groups of a) isolation, b) quarantine and c) physical distancing.

The researchers will assess changes in adherences over time within participant groups a) isolation, b) quarantine, using chi-square tests of proportions. The researchers will assess changes in adherence to government requirements within participant group c) physical distancing over time, using time to event analysis, such as proportional hazards tests or Cox regression.

Researchers are not using individual assessments for analyses.

18 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Margaret Hellard, The Macfarlane Burnet Institute for Medical Research and Public Health

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)

September 30, 2020

Primary Completion (Estimated)

June 30, 2024

Study Completion (Estimated)

June 30, 2024

Study Registration Dates

First Submitted

April 6, 2022

First Submitted That Met QC Criteria

April 10, 2022

First Posted (Actual)

April 12, 2022

Study Record Updates

Last Update Posted (Actual)

October 23, 2023

Last Update Submitted That Met QC Criteria

October 18, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

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 COVID-19

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