We’re looking for volunteers with Asthma to participate in a paid at-home sleep study. You could improve the quality of sleep for Asthma sufferers – and be compensated for your participation.
First, sign up with your email and fill out a short questionnaire to find out whether you qualify for the study. If you do, a Patient Experience Coordinator will contact you to set up a time to finish the pre-screening process. If you are a match and want to participate, we’ll walk you through the steps for enrollment and the informed consent process. This process helps you understand what is expected, what your role is, and how the study works.
During the five-week study screening period, there will be a remote consenting visit conducted via telemedicine, and up to two (2) visits at your home to check whether this study is right for you. Once the study doctor confirms your eligibility, you will enter the 12 week treatment period. This includes 2 visits at the start of the treatment period within 1-3 days of each other, and 3 more study nurse visits completed in your home once every 4 weeks. There will also be a final visit conducted remotely, or an early discontinuation visit with a home nurse if you or your study doctor decide on early withdrawal.
This study uses many assessments/questionnaires/diaries to ask you several questions, including questions about asthma, sleep, and quality of life. You will be required to wear a wristwatch called Actiwatch, 24 hours per day, except for bathing and showering. The Actiwatch takes measurements associated with sleep. The at-home visits may also require a breathing test, and blood and urine samples. After the treatment period is complete, you will have one follow up phone call with the study doctor to check your health after you finish using the study drug. This study is open to adult participants ages 18 to 65 years old, who have a confirmed Asthma diagnosis.
A clinical research coordinator will discuss the study with you in a telemedicine visit (phone call).
Meet with a study team member, via a phone call or at-home, for study consent and again 12 weeks following the end of the study treatment period.
We have an awesome team of doctors, researchers, and patient experience coordinators who are eager to help guide you through the research process.