Does Continuous Vital Sign Monitoring Increase Investigations and Interventions in Complication-free Patients? (WARD-OT)

Rigshospitalet

Status: Enrolling

Conditions: Surgery-Complications; Chronic Obstructive Pulmonary Disease; Cancer

Treatments: Device: Active alarms from WARD software

Study type: Interventional

Funder types: Other

Identifiers

NCT06361862

WARD - Overtreatment

Details and patient eligibility

About

This aim of this study is to investigate whether active alerts during CVSM result in an increased number of diagnostic tests and treatments in complication free patients, hypothesizing that more interventions are performed in the CVSM-group than standard of care (EWS) group.

Enrollment: 700 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• • Patients from WARD - RCT.

Exclusion criteria

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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700 participants in 2 patient groups

inactive alarms

No Intervention group

Description:

Patients with continuous monitoring without active alerts from WARD.

active alarms

Experimental group

Description:

Patients with continuous monitoring with active alerts from WARD.

Treatment:

Device: Active alarms from WARD software