Respiratory Research Study

Written By Shawn C

May - August 2024

We are seeking participants with respiratory symptoms for sample collection

 

How to take part in the study?

To take part in our research study, you must meet the following criteria:

  • Have respiratory symptoms such as fever, runny nose, shortness of breath, nasal congestion, sore throat

  • Sample collection must be within 7 days of symptom onset

Next steps:

  • Click the button below to book a Respiratory Infection Appointment at Key Health Medical Centres via HotDoc

  • Arrive at your scheduled appointment, the Key Health team will explain the process and review your eligibility for the research study

  • If you are eligible, you will need to provide your consent to participate, at least 2 nasal swabs and demographic information (age, gender, symptoms, current medications, vaccination status)

  • Successful participants will receive compensation for their time and effort

Respiratory Research
 

Trial Locations

The respiratory research study is available at the following Key Health Medical Centres:

 

Key Health CBD South

Ground Floor, 281 Elizabeth Street
Sydney NSW 2000
Phone: (02) 8262 1000

 

Key Health Bondi Junction

47 Spring Street,
Bondi Junction NSW 2022
Phone: (02) 8262 1800

 

Key Health Pagewood

Shop 1, 11 Oscar Place,
Eastgardens NSW 2036
Phone: (02) 8267 2122

 

Compensation must be appropriate for trial participants; Recruitment material, research study and proposed payments to participants have been approved by the relevant Human Research Ethics Committee (HREC); Clinical trial sponsors in Australia are expected to comply with the National Statement on Ethical Conduct in Human 'Research (National Statement) and the ICH Guideline for Good Clinical Practice OCH Guideline). Generally speaking, it is permissible under the National Statement to reimburse participants for the time and effort associated with participating in the research, provided the amount paid is proportionate to the level of participation, and does not induce or place pressure on individuals to consent to participate (National Statement, 2.2.10). The HREC for the trial is responsible for reviewing and considering the trial procedures and recruitment materials to ensure that they are appropriate (National Statement, 5.2.25, and ICH Guideline, 441)

DSM-PROT-005190-A - Clinical Study Protocol 1 05190-A Key Health Advertising Website V1.0_05Apr2024

Shawn C
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