Creating A Risk Assessment Tool for Thunderstorm Asthma: the CARISTA Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorUniversity of Melbourne

About this trial

Thunderstorm asthma is a recurring public health emergency in South-Eastern Australia which occurs in springtime. The major identified risk factors for thunderstorm asthma is hay fever and allergy to ryegrass pollen. The goal of the CARISTA study is to identify the risk of springtime allergic and thunderstorm asthma in allergic adults living in South-Eastern Australia. To do this the investigators will recruit 530 people who have hay fever and test them for allergy to ryegrass pollen and undertake simple lung function testing. The investigators will ask study participants to complete a customised symptom tracker over the springtime pollen season for 2 consecutive years. The outcome the investigators are looking for is an asthma exacerbation or worsening asthma symptoms. This study will enable the investigators to identify indicators (biomarkers) of severe and moderate asthma exacerbations in order to identify those at risk of thunderstorm and seasonal asthma so protective treatments and strategies can be advised.

Eligibility criteria

Qualifiers

Lung function testing

Blood sample collection for risk factor identification, -Prospectively logging their symptoms and medications through the springtime season using the CARISTA symptom monitoring platform . -

Disqualifiers

Individuals unable to provide informed consent

Individuals who do not suffer from symptoms of seasonal allergic rhinitis

Individuals who do not consent to lung function testing and blood sample collection - Individuals with unstable asthma (FEV1 by spirometry less than 70% predicted), a recent exacerbation or change of asthma preventive medication use (within one month) would be excluded, although re-screening would be permitted after one month, time permitting.

Individuals with severe asthma requiring the use of continuous oral corticosteroids or biological medication for severe asthma.

Trial design

Treatments tested in this trial

  • Observational

Treatment groups

530 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Melbourne

Lead sponsor

The Alfred

Collaborator

Eastern Health

Collaborator

Austin Hospital, Melbourne Australia

Collaborator

Monash Medical Centre

Collaborator

Queensland University of Technology

Collaborator

Northern Hospital, Australia

Collaborator

Western Hospital, Australia

Collaborator

Melbourne Health

Collaborator