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

Recruiting N/A Interventional Study
Vital Sign Evaluation Vital Sign Monitoring Sleep Quality Provider Behavior Patient Satisfaction
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
270 (estimated)
Sponsor
Northwestern University · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
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.
Contacts

Gregory (Randy) R Smith Jr, MD MS

312-926-5893

g.smith@nm.org

CONTACT

Jane S Kim, MS MEd

312-926-7272

jane.kim@northwestern.edu

CONTACT