Actively Recruiting

Age: 18Years +
All Genders
ID07026773

Validity of ICU Clinician's Appraisal of Proportionality in CPR in Patients Treated for Out-of-Hospital Cardiac Arrest

Led by University Hospital, Ghent · Updated on 2025-06-18

1000

Participants Needed

9

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how well doctors and nurses in Intensive Care Units (ICUs) can predict neurological outcomes and quality of life six months after patients experience cardiac arrest outside the hospital. This study compares ICU clinicians' early assessments within 24 hours after admission to the results of a detailed neuroprognostication process from the STEPCARE study, which aims to find the best post-resuscitation care strategies to improve survival and neurological outcomes. The study involves ICU doctors and nurses treating patients enrolled in the STEPCARE study. Within the first 24 hours after ICU admission, these clinicians complete a brief survey about their perceptions of each patient's frailty, quality of life, comorbidities, appropriateness of CPR, and expected outcomes. Their judgments will be compared with the STEPCARE study's multimodal neuroprognostication results, which use clinical exams, tests, and imaging to predict outcomes. Participants in this study are ICU clinicians caring for patients who had out-of-hospital cardiac arrest and are part of STEPCARE. The research team will analyze how well clinicians' views match the detailed neuroprognostication and examine the added value of combining both approaches to predict survival with good function and quality of life at six months. The study collects survey responses and clinical data to measure these outcomes and is supported by statistical methods to assess predictive accuracy and agreement.

CONDITIONS

Brief Title

Validity of ICU Clinician's Appraisal of Proportionality in CPR

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Doctors and nurses working in the Intensive Care Unit treating patients included in the STEPCARE study (NCT 05564754)
Not Eligible

You will not qualify if you...

  • Doctors and nurses who do not have a direct treatment relationship with a patient included in the STEPCARE study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit

Monitoring

Duration - Within 24 hours after ICU admission

Participants who are ICU doctors and nurses complete a short survey within 24 hours of ICU admission of patients included in the STEPCARE study, capturing their clinical appraisal regarding appropriateness of CPR and prognostication.

1 survey completion (short, less than 3 minutes)

Long-term Monitoring

Duration - Up to 6 months after return of spontaneous circulation

Participants' perceptions and prognostications are compared with multimodal ICU neuroprognostication results and patient outcomes, including survival and neurological function at 6 months after out-of-hospital cardiac arrest.

Follow-up assessments aligned with STEPCARE study outcomes

Trial Site Locations

Total: 9 locations

1

Medical University Innsbruck

Innsbruck, Austria, 6020

Not Yet Recruiting

2

Ziekenhuis Oost-Limburg

Genk, Belgium, 3600

Actively Recruiting

3

Ghent University Hospital

Ghent, Belgium, 9000

Actively Recruiting

4

Helsinki University Central Hospital

Helsinki, Finland, 000290

Not Yet Recruiting

5

Universitätsklinikum Lübeck

Lübeck, Germany, 23538

Actively Recruiting

6

Policlinico San Martino

Genova, Italy, 16149

Actively Recruiting

7

Wakefield Hospital

Wellington, New Zealand, 6021

Actively Recruiting

8

King Abdulaziz Medical City

Riyadh, Saudi Arabia, 22490

Actively Recruiting

9

Zürich University Hospital

Zurich, Switzerland, 8091

Not Yet Recruiting

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Research Team

P

Patrick Druwé, MD, PhD

D

Daisy Vermeiren, Research Nurse

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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