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CSAPG Early Warning Score

CSAPG Early Warning Score

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04905095
Acronym
CEWS
Enrollment
15998
Registered
2021-05-27
Start date
2021-06-01
Completion date
2024-12-31
Last updated
2025-02-12

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

Conditions

Undefined

Keywords

Hospital Stay, Mortality, Clinical Deterioration

Brief summary

The Early Warning Score (EWS) has been shown in previous studies to be correlated with mortality and mean hospital stay, but it is unknown whether the implementation of the scale improves mortality and mean hospital stay. This trial aims to study whether the implantation of the EWS in a regional hospital reduces the mean hospital stay (primary objective), mortality and complications (secondary objectives). For this, an open clinical trial will be carried out in which the hospitalization floors of the hospital will be administratively divided into two sections (two study branches); the EWS scale will be implemented in the computer equipment of one of the sections of each floor, acting the another section as a control branch. All the patients admitted to the participating hospital floors during one year will be included in the study. The mean stay, mortality and complications will be compared between study branches.

Interventions

OTHEREWS

Early Warning Score will be implemented in the computer system of the nursing station which belong to this intervention group. When the nurses enter the vital signs of the patients into the system, the EWS will be automatically calculated and an alarm will be displayed if an intervention is necessary, which is protocolized.

Nurses perform their clinical monitoring activities as usual. EWS will not be implemented in their nursing station

Sponsors

Consorci Sanitari de l'Alt Penedès i Garraf
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients admitted during study period to the participant hospital units.

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Hospital stayfrom baseline to hospital discharge, as much 3 monthsAverage days of hospital admission

Secondary

MeasureTime frameDescription
Mortalityfrom baseline to hospital discharge, as much 3 monthsPercentage of patients deceased during hospital admission
Complicationsfrom baseline to hospital discharge, as much 3 monthsPercentage of patients who develop health complications during hospital admission

Countries

Spain

Outcome results

None listed

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