The Vital Signs to Identify, Target, and Assess Level (VITAL) Care Study III

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

446 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-10-05

Study Completion Date

2017-02-28

Brief Summary

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To evaluate the effect of automated recording on frequency of recorded scores, number of automated notifications and serious events.

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Detailed Description

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The frequency of EWS scores, number of automated notifications and serious events performed on a general ward is contingent on the quality and frequency of vital signs measurement like respiratory rate. This is due to the EWS escalation schemes of hospitals with an acute intervention team. Obtained sub-score trigger levels of vital signs contribute to higher and more frequent scoring.

We examine the influence of different respiration rate sensor concepts and measurements on scoring (NEWS and CREWS) and workflow in a typical UK gastroenterology and respiratory ward.

Conditions

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Cardiac Arrest Renal Failure Respiration Failure Myocardial Infarction Severe Sepsis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Manual Respiration Rate Measurement

Patients with manually measured respiratory rate

No interventions assigned to this group

Automatic Respiration Rate Measurement

Patients with automatically measured respiratory rate

Automatic RR Measurement

Intervention Type DEVICE

Different newly developed respiration rate sensors are applied at the bedside during the intervention phase which send data to the IntelliVue Guardian System.

Interventions

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Automatic RR Measurement

Different newly developed respiration rate sensors are applied at the bedside during the intervention phase which send data to the IntelliVue Guardian System.

Intervention Type DEVICE