The Internal Prospective Validation of the Cancer Admission Score (CAS) Prediction Model (ONCOMING)

August 12, 2025 updated by: Jason den Duijn, Erasmus Medical Center

The Internal Prospective validatiON of a prediCtiOn Model for the Change of admIssion for Patient With caNcer Admitted to the emerGency Department (ONCOMING Study)

The goal of this single center prospective observational study is to determine the agreement between the cancer admission score (CAS) predicted disposition and the actual disposition in patients with an active cancer diagnosis visiting the emergency department (ED). The main question it aims to answer are: Is the performance of the CAS good enough to play a potential role in the ED care process. For each participant the CAS will be calculated and compared to the actual outcome.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The goal of this single center prospective observational study is to determine the agreement between the cancer admission score (CAS) predicted disposition and the actual disposition in patients with an active cancer diagnosis visiting the emergency department (ED). The main question it aims to answer are: Is the performance of the CAS good enough to play a potential role in the ED care process.

The first part of this study is an observational part. For patients with cancer that are presented to the emergency department (ED) the cancer admission score (CAS) will be calculated by the model both after triage and after the first blood results are in. Furthermore, the expected disposition will be asked to the attending nurse after triage and after the first blood results. Finally, the actual disposition will be written down after the patient has left the ED, in combination with ED length of stay (LOS) and the time for the attending physician to reach a decision about the disposition (time-to-disposition) and the time for a patient to leave the ED (time-to-leave).

The second part is the interventional part. In this part we introduce an early bed reservation intervention. The CAS is still calculated for the patient. If the CAS is 80% or higher based on the triage, the attending physician will be alerted and a call to the bed coordinator will be placed to reserve a bed in advance. After the first blood results are known the second CAS will be calculated, if this drops below 70% the reserved bed can be canceled by the attending physician. Similar to the first part, the expected disposition from the attending nurse after triage and after first blood results will be collected. Finally, the actual disposition, ED LOS, time-to-disposition and time-to-leave will be noted.

Study Type

Observational

Enrollment (Estimated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Zuid-Holland
      • Rotterdam, Zuid-Holland, Netherlands, 3015GD
        • Recruiting
        • Erasmus University Medical Center
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

All adult patients with an active cancer diagnosis who visit the ED of the Erasmus University Medical Center (Erasmus MC).

Description

Inclusion Criteria:

  • Patients with solid or hematological malignancies and receiving systemic therapy or having received systemic therapy within the last 3 months.
  • Presented at or admitted from the emergency department for the oncology, hematology neuro- or lung-oncology clinical unit.

Exclusion Criteria:

  • <18 years old
  • Only received a surgical intervention as cancer treatment
  • Admitted to the ED for the surgical department

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Cancer patients
All adult patients with an active cancer diagnosis who visit the emergency department (ED) of the Erasmus University Medical Centre (Erasmus MC).
A prediction model that calculates the chance for a patient to be admitted after triage and after first blood results

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Disposition
Time Frame: Through study completion, an average of 6 months
The outcome of a visit to the ED, being either admission or home
Through study completion, an average of 6 months
Agreement between the CAS and the actual disposition
Time Frame: Through study completion, an average of 6 months
Agreement between the CAS predicted outcome and the actual outcome
Through study completion, an average of 6 months
Cancer Admission Score
Time Frame: Through study completion, an average of 6 months
Cancer Admission Score (CAS) calculated after triage and after first blood results, ranging from 0 to 100%. The higher the score the greater the change of admission
Through study completion, an average of 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Agreement between expected disposition by nurse and actual disposition
Time Frame: Through study completion, an average of 6 months
Agreement between the nurse predicted outcome and the actual outcome
Through study completion, an average of 6 months
time-to-disposition
Time Frame: Through study completion, an average of 6 months
The average time between patient's arrival at the emergency department (ED) and the decision to disposition
Through study completion, an average of 6 months
time-to-leave
Time Frame: Through study completion, an average of 6 months
The average time between the decision to disposition and departure from the ED (either home or ward)
Through study completion, an average of 6 months
ED Length of Stay
Time Frame: Through study completion, an average of 6 months
The total time spent in the ED by a patient during their visit
Through study completion, an average of 6 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sex
Time Frame: Through study completion, an average of 6 months
The sex of a patient
Through study completion, an average of 6 months
Age
Time Frame: Through study completion, an average of 6 months
The age of a patient
Through study completion, an average of 6 months
Type of Cancer
Time Frame: Through study completion, an average of 6 months
The type of cancer a patient has
Through study completion, an average of 6 months
Type of Treatment
Time Frame: Through study completion, an average of 6 months
Type of cancer treatment a patient receives
Through study completion, an average of 6 months
Main Complaint
Time Frame: Through study completion, an average of 6 months
Main complaint of ED visit
Through study completion, an average of 6 months
Physical parameters recorded during triage
Time Frame: Through study completion, an average of 6 months
Physical parameters that are recorded during triage and are used in the prediction model
Through study completion, an average of 6 months
First Blood results
Time Frame: Through study completion, an average of 6 months
The blood results that are recorded during triage and are used in the prediction model
Through study completion, an average of 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jason den Duijn, Erasmus Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 2, 2024

Primary Completion (Estimated)

December 1, 2025

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

August 14, 2024

First Submitted That Met QC Criteria

August 14, 2024

First Posted (Actual)

August 16, 2024

Study Record Updates

Last Update Posted (Estimated)

August 15, 2025

Last Update Submitted That Met QC Criteria

August 12, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 12821

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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