Resmed Clinical Research
Help us by volunteering for our trials where you can be the first to test and provide feedback on our next generation of products.
About Resmed Clinical Research
What is the Research Registry?
Our registry is a database of volunteers that we may contact from time to time, based on the needs of research studies. During sign-up, you will be asked for information that will be used to contact you by our Research team.
Who can participate?
Clinical research is open to individuals 18 years of age and older located in the United States. We encourage individuals of all backgrounds and abilities to join whether you have a sleep/respiratory condition or not.
Participate in our research
It’s our mission to improve our products to help all people to awaken their best.
How to be part of the Research Registry
Step 1
Read the Resmed Information Statement to make sure you understand and agree with how we will use and disclose your information prior to signing up. Then click below to sign up for Resmed Research Registry.
Sign up for the research registry:
Step 2
The Resmed Research team will contact you via email, phone, and/or text message when a suitable research opportunity becomes available via the contact information you provided us from the research registry.
Frequently asked questions
Research studies can be in person, online, via video, or mailed out. Some studies will involve clinical data while others will not. Most research studies require a single interaction with Resmed, however, other studies may require you to receive products and try them at home. On average, take-home studies typically require 2-3 visits or check-ins, depending on the research question and study. Each study has its own information sheet that will clearly state the participant’s commitment. In person visits are typically conducted in our office in San Diego, CA.
The number one thing we require from you is your feedback and opinion to ensure we are providing our users the best services and products we can. These clinical trials evaluate our product designs and are never a test about you. We typically ask questions about your understanding of the product instructions, and whether you use our devices as intended. Each clinical study has a participant information sheet and consent form that will explain in detail what is expected from you. Your study participation is always voluntary.
If you volunteer to register for the Resmed Research Registry, we will collect your personal information and some health information from or about you, to provide us with feedback aimed at improving product innovation and the patient experience, as well as to help us improve our offered products and therapy delivery. For full details, please read our Information Statement and Privacy Policy.
Participation in all clinical trials requires an assessment of risk. The Resmed Research team will explain all applicable risks associated with the clinical trial in our Participant Information and Consent Form, which is tailored for each study.
Participating in the research registry is voluntary and free of charge to you. For some studies, you may be reimbursed for your time and participation. In those circumstances, the amount you will be paid will be specified in the study specific Participant Information and Consent Form after you have been invited to participate.