AFib Data Collection
Study Number: C24-D013
Study Location:
Dallas Research Center: 1801 N. Glenville Dr., Suite 250 Richardson, Texas 75081
Compensation: Up to $700
Gender:
Males and Females
Age:
22+
Skin Type:
I-VI (Light to dark skin tones)
Study Description:
The purpose of this study is to collect data from individuals with AFib by wearing a currently marketed smart watch.
Study Requirements:
- Must have a history of persistent and/or paroxysmal AFib.
- Must be either pre-ablation/surgery OR have undergone AFib ablation or procedure to restore the heart rhythm in the past 90 days.
- Cannot have a implantable device, such as a pacemaker, or implantable cardioverter-defibrillator, ventricular assist device or artificial heart.
- Cannot have any known allergies to adhesives or dry skin that is irritated by adhesives.
- Cannot have any allergies or sensitivities to watch or watch band materials, such as stainless steel, aluminum, titanium, and ceramics.
- Cannot currently be participating in another clinical trial that involves an investigational drug or device.
Visit 1 Instructions
- Bring a valid ID or passport.
- Bring your documentation of your Afib diagnosis.
- Your first visit could take up to 2.5-3 hours.
- If you are not able to make your appointment, please contact us ASAP by calling us at 833-530-7596.
Complete the prescreening survey below
All information you provide will be kept confidential, you may be contacted by telephone or text, and your information may be added to a database.