Skip to content

Professional Development in Emergency Medical Services

Efficacy of a Clinical Decision Support System in Prehospital Care: Single Blind, Randomized Clinical Trial.

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02365792
Acronym
ProDEms
Enrollment
0
Registered
2015-02-19
Start date
2016-06-30
Completion date
2025-12-31
Last updated
2023-08-31

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

Conditions

Clinical Decision Support, Clinical Practice Guidelines, Emergency Medical Services

Keywords

Clinical Decision Support, Clinical Practice Guidelines, Emergency Medical Services

Brief summary

The ProDEms-trial focuses on nurses and ambulance drivers working in prehospital care, taking care on the one hand of patients suffering from time-sensitive critical conditions like STEMI, acute stroke or severe traumatic brain injury, and on the other hand of patients whose lives are not in immediate danger but suffer from acute exacerbation of chronic conditions or suffer from acute pain. In the current study the investigators will use a multistage approach to test the hypothesis whether the use of a CDSS in prehospital emergency care will: 1. Improve protocol adherence, 2. Reduce emergency department length of stay, 3. Improves diagnostic accuracy; without impeding the workflow of the prehospital team or impairing patient safety.

Interventions

PROCEDUREClinical Decision Support Tool for Prehospital Care

A clinical decision support system (CDSS) is a health information technology system that is designed to assist physicians and other health professionals with clinical decision-making tasks. A working definition of the Centre for Health Evidence: Clinical Decision Support systems link health observations with health knowledge to influence health choices by clinicians for improved health care.

Sponsors

KU Leuven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
1 Years to 112 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients who receive treatment from the Paramedic Intervention Team (PIT) in the prehospital Emergency Medical Services (EMS) area of the University Hospitals, Leuven.

Exclusion criteria

* Patient-related interventions not dispatched by the Emergency Medical Dispatch center (EMD) * Patient related interventions during transport between two healthcare facilities or in mass casualty situations.

Design outcomes

Primary

MeasureTime frameDescription
Treatment protocol adherenceUp to 12 monthsMeasured by comparing the prescribed actions to be taken following the selected standing order (-s) or procedures, with the actual action (-s) taken.

Secondary

MeasureTime frameDescription
Length of Stay in the EDUp to 12 monthsMeasured as the duration between the times the patient is assigned with a unique EAD number in the emergency department and the disposition decision is marked in the Electronic Patient Record (EPR), indicating that the patient is ready to be discharged from the ED.
Prehospital Patient Time IntervalUp to 12 monthsMeasured as the duration between the arrival time at the scene and and arrival time at the ED.
Consistency in reported diagnose and the choice of PIT standing order (-s) or procedure (-s)Up to 12 monthsMeasured by comparing the selected standing order (-s) or protocol (-s) and the reported diagnose (-s).
Alignment between diagnostic accuracy and interventions taken.Up to 12 monthsMeasures by comparing the use of available scales and the corresponding prescribed action (-s) to be taken following the standing orders.

Countries

Belgium

Outcome results

None listed

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