270
Participants
Start Date
June 2, 2025
Primary Completion Date
July 31, 2026
Study Completion Date
July 31, 2026
Device Array Use
Study participants assigned to the intervention study arm will wear a wireless Bluetooth capable vital sign detection array, with one device externally worn on each of their chest, one finger, and one arm, with healthcare providers using an additional oral temperature probe.
Routine Vital Sign Measurement
Study participants randomized to the control arm will have their vital signs obtained by routine means, without use of the wireless vital sign device array.
RECRUITING
Feinberg 16 West, Northwestern Memorial Hospital, Chicago
NOT_YET_RECRUITING
Northwestern Memorial Hospital, Chicago
University of Minnesota Medical School/University of Minnesota Foundation
UNKNOWN
Sibel Health Inc.
INDUSTRY
Northwestern University
OTHER