RECRUITING

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

Description

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.

Study Overview

Study Details

Study overview

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.

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

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

Condition
Vital Sign Evaluation
Intervention / Treatment

-

Contacts and Locations

Chicago

Feinberg 16 West, Northwestern Memorial Hospital, Chicago, Illinois, United States, 60611

Chicago

Northwestern Memorial Hospital, Chicago, Illinois, United States, 60611

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Inpatients admitted to Northwestern Memorial Hospital, Feinberg Unit 16 West.
  • * Primary language other than English, under isolation status, pregnant patients, prisoners, employees or students of the hospital or Northwestern University.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Northwestern University,

Gregory (Randy) R Smith Jr, MD MS, PRINCIPAL_INVESTIGATOR, Northwestern University Feinberg School of Medicine

Study Record Dates

2026-07-31