Purpose of this Study
We are doing this study is to see if we can predict carotid artery function using wearable technology (for example, a FitBit®).
Who Can Participate?
Eligibility
We are enrolling 2 different types of candidates in this study:<ul>
<li>Cohort 1: Healthy adults ages 18+ who do not have any ongoing medical conditions that require regular medical care and/or routine medication (these participants will be the comparison group).</li>
<li>Cohort 2: Adults ages 18+ who are diagnosed with carotid artery stenosis and are undergoing carotid artery revascularization.</li></ul>
For more information, contact the study team at <a href= "mailto: frank.benedetti@duke.edu">frank.benedetti@duke.edu.</a>
<li>Cohort 1: Healthy adults ages 18+ who do not have any ongoing medical conditions that require regular medical care and/or routine medication (these participants will be the comparison group).</li>
<li>Cohort 2: Adults ages 18+ who are diagnosed with carotid artery stenosis and are undergoing carotid artery revascularization.</li></ul>
For more information, contact the study team at <a href= "mailto: frank.benedetti@duke.edu">frank.benedetti@duke.edu.</a>
Age Range
18-110
Sex/Genders
Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
Yes
What is Involved?
If you agree to participate, you will be asked to wear a FitBit for 18 months. You will also have up to four ultrasounds taken at the following times after your carotic artery procedure:<ul>
<li>1 month</li>
<li>6 months</li>
<li>12 months</li>
<li>18 months</li></ul>
Data from these ultrasounds will be collected and compared to the data recorded on the FitBit.
<li>1 month</li>
<li>6 months</li>
<li>12 months</li>
<li>18 months</li></ul>
Data from these ultrasounds will be collected and compared to the data recorded on the FitBit.
Locations
Duke University Hospital
Visit Timing
Weekdays
Compensation
No
Spanish Materials Available
No
Study Details
Full Title
Prediction of Carotid Artery Stenosis using Wearable Technology
Principal Investigator
Kevin
Southerland
Protocol Number
PRO00114171
Phase
N/A
Enrollment Status
Open to Enrollment