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

Northwestern University

Status: Enrolling

Conditions: Sleep Quality; Patient Satisfaction; Vital Sign Monitoring; Provider Behavior; Vital Sign Evaluation

Treatments: Device: Routine Vital Sign Measurement; Device: Device Array Use

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06995742

2023 Dixon Translational Grant (Other Grant/Funding Number)

STU00219340

Details and patient eligibility

About

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.

Enrollment: 270 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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270 participants in 2 patient groups

Intervention--Device Array Use

Experimental group

Description:

Inpatients will wear the ANNE One device array for obtainment of vital sign assessments.

Treatment:

Device: Device Array Use

Control--Routine Vital Sign Obtainment

Active Comparator group

Description:

Inpatients will have vital signs determined by routine practice, using any other standard of care-accepted method or device.

Treatment:

Device: Routine Vital Sign Measurement