Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:16 AM
Ignite Modification Date:
2025-12-25 @ 2:16 AM
NCT ID:
NCT02450760
Eligibility Criteria:
Inclusion Criteria:
* Adult, age ≥ 18 years
* History of ischemic stroke or high risk TIA (defined by ABCD2 ≥ 4)between 2 weeks and 12 months prior to enrollment
* Hypertensive at time of enrollment, defined by SBP\>140 mm Hg or DBP \>90 mm Hg at the time of study screening
* Must own a smart phone capable of interacting with the connected blood pressure cuff (Apple iPhone 3GS or higher; Android 4.0 or higher with Bluetooth connectivity)
* Willingness and ability to sign informed consent by patient
Exclusion Criteria:
* Moderate or severe disability, defined by modified Rankin Scale ≥ 3.
* Expected residence in a rehabilitation hospital, nursing facility or assisted living community during the study period.
* Upper arm circumference \<9 inches or \>17 inches
* Inability to monitor BP in both of the upper arms (i.e. history of bilateral radical mastectomy, bilateral severe subclavian stenosis, or bilateral arterial venous fistulas for dialysis).
* Blood pressure discrepancy between arms of \>10 mm Hg.
* Inability to follow-up at 90 days and return BP monitor
* Active participation in another clinical trial
* Pregnant women
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02450760
Study Brief:
Protocol Section:
NCT02450760