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

NCT07055542 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 530

Last updated 2026-05-06

No results posted yet for this study

Summary

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.

Conditions

  • Allergic Asthma
  • Thunderstorm Asthma
  • Seasonal Allergic Rhinitis
  • Grass Pollen Allergy
  • Asthma Exacerbation Due to Thunderstorm
  • Asthma Acute

Interventions

DIAGNOSTIC_TEST

Observational

Prospective observational study

Sponsors & Collaborators

  • The Alfred

    collaborator OTHER
  • Eastern Health

    collaborator OTHER
  • Austin Hospital, Melbourne Australia

    collaborator OTHER
  • Monash Medical Centre

    collaborator OTHER
  • Queensland University of Technology

    collaborator OTHER
  • Northern Hospital, Australia

    collaborator OTHER
  • Western Hospital, Australia

    collaborator OTHER_GOV
  • Melbourne Health

    collaborator OTHER
  • University of Melbourne

    lead OTHER

Principal Investigators

  • Jo A Douglass, MD · University of Melbourne & Royal Melbourne Hospital

  • Phillip Bardin, MD · Hudson Institute of Medical Research

  • Frank Thien, MD PhD · Eastern Health

  • Mark Hew, MD PhD · The Alfred

  • Janet Davies, PhD · Queensland University of Technology

  • Fay Johnston, PhD · University of Tasmania and AIRHealth PtyLtd

  • Edwin Lampugnani, PhD · AirHealth Pty Ltd

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-08-27
Primary Completion
2029-12-31
Completion
2030-12-31

Countries

  • Australia

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07055542 on ClinicalTrials.gov