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.
Fill out the fields below to apply!
Please note: You must be using Safari, Firefox or Chrome to apply.
All information you provide will be kept confidential, you may be contacted by telephone, and your information may be added to a database.