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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02973243
Enrollment
446
Registered
2016-11-25
Start date
2016-10-05
Completion date
2017-02-28
Last updated
2017-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest, Myocardial Infarction, Renal Failure, Respiration Failure, Severe Sepsis

Keywords

early warning scoring, respiration rate, acute care teams, NEWS, CREWS

Brief summary

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

Detailed description

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.

Interventions

DEVICEAutomatic 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.

Sponsors

Philips Healthcare
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients admitted to the study units during the period of data collection

Exclusion criteria

* palliative patients

Design outcomes

Primary

MeasureTime frame
Number of NEWS Scores8-12 Weeks

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026