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Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity
Sponsor: Northwestern University
Summary
Randomized controlled trial of a time motion study of time spent obtaining and charting vital signs for inpatients, comparing use of a wireless Bluetooth vital sign array as intervention versus routine vital sign obtainment activity on a general medical floor.
Official title: Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity: A Randomized Controlled Trial
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
270
Start Date
2025-06-02
Completion Date
2026-07-31
Last Updated
2025-06-05
Healthy Volunteers
No
Conditions
Interventions
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.
Locations (2)
Feinberg 16 West, Northwestern Memorial Hospital
Chicago, Illinois, United States
Northwestern Memorial Hospital
Chicago, Illinois, United States