Read the ResMed Information Statement to make sure you understand and agree with what we do with your information prior to signing up. Then click below to sign up for ResMed Clinical Research.
The ResMed Research team will contact you via SMS, phone, and/or email when a suitable research opportunity becomes available via the provided contact information from the registry.
Studies can be face-to-face, online, or mailed out. Most studies require a single visit other studies require products to be taken home and trialled, these studies typically are 2-3 visits however it will depend on the research question. Each study has its own Information sheet that clearly states the commitment. Face to face visits are typically in Sydney. Online or mail out studies can be anywhere in Australia.
The number one thing we require is your feedback, and opinion to ensure we are servicing our customers the best we can. These trials evaluate our designs and are never a test of you. Questions we ask typically involve whether you can understand the instructions, and whether you can use the device as the designer intended. Each study has a participant information and consent sheet that explains in detail what is expected. Study participation is always voluntary.
All trials require an assessment of risk. All risks will be explained in our Participant Information and Consent Sheet which is tailored for each study.
Participating in the registry is voluntary, free of charge and without obligation. In some circumstances, you may be reimbursed for your time and participation. In that case, the amount will be specified in the study specific Participant Information and Consent sheet.