Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity

NARecruitingINTERVENTIONAL
Enrollment

270

Participants

Timeline

Start Date

June 2, 2025

Primary Completion Date

July 31, 2026

Study Completion Date

July 31, 2026

Conditions
Vital Sign EvaluationVital Sign MonitoringSleep QualityProvider BehaviorPatient Satisfaction
Interventions
DEVICE

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.

DEVICE

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.

Trial Locations (2)

60611

RECRUITING

Feinberg 16 West, Northwestern Memorial Hospital, Chicago

NOT_YET_RECRUITING

Northwestern Memorial Hospital, Chicago

All Listed Sponsors
collaborator

University of Minnesota Medical School/University of Minnesota Foundation

UNKNOWN

collaborator

Sibel Health Inc.

INDUSTRY

lead

Northwestern University

OTHER

NCT06995742 - Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity | Biotech Hunter | Biotech Hunter