This is a prospective, unblinded sub-study to the E-30 to gather physiological data.
This sub-study to the E-30 is designed to collect vital signs, accelerometer and ECG data on subjects, and will consist of two phases. Phase 1 is designed to collect data in an Epilepsy Monitoring Unit (EMU) and Phase 2 is designed to collect data in an everyday (ambulatory) setting.
Study Type
INTERVENTIONAL
Allocation
NA
Masking
NONE
Enrollment
16
A sensor platform that enables physiological monitoring in routine, home or office environments.
Unnamed facility
Gainesville, Florida, United States
Unnamed facility
Chicago, Illinois, United States
Gather physiological data
The purpose of this sub-study is to gather physiological data in consenting subjects who were previously enrolled in the "parent" E-30 study (NCT01202669).
Time frame: Up to 2 weeks
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