RecruitingNot ApplicableNCT06995742

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

Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity: A Randomized Controlled Trial

Sponsor

Northwestern University

Enrollment

270 participants

Start Date

Jun 2, 2025

Study Type

INTERVENTIONAL

Conditions

Patient Satisfaction Sleep Quality Vital Sign Monitoring Vital Sign Evaluation Provider Behavior

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.

Eligibility

Min Age: 18 Years

Inclusion Criteria1

Inpatients admitted to Northwestern Memorial Hospital, Feinberg Unit 16 West.

Exclusion Criteria1

Primary language other than English, under isolation status, pregnant patients, prisoners, employees or students of the hospital or Northwestern University.

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Interventions

DEVICEDevice 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.

DEVICERoutine 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.