Actively Recruiting

Age: 18Years +
All Genders
ID06960642

Early Rehabilitation of Intensive Care Unit Patients - a Multinational Prospective Observational Study on Dosage and Outcome

Led by Medical University of Vienna · Updated on 2026-02-20

6000

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

M

Medical University of Vienna

Lead Sponsor

E

European Society of Intensive Care Medicine

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to study the early rehabilitation and mobilisation practices for patients in intensive care units (ICUs) worldwide. It focuses on understanding how different mobilisation approaches affect physical function, functional status, and quality of life in ICU patients. The study addresses the issue of Intensive Care Unit Acquired Weakness (ICUAW), which affects around 40% of ICU patients and leads to long-term functional limitations and reduced independence. Researchers want to find the best mobilisation dosage to improve patient outcomes, including those who were dependent before ICU admission or not on invasive mechanical ventilation. The study is a multinational, prospective observational trial involving over 6,000 patients from at least 200 ICUs. It does not involve any interventions but collects routine clinical and mobilisation data during ICU stays. Patients are categorized based on their functional independence before ICU admission. Participation lasts 90 days per patient, within a total study duration of 21 months. Standardized physical tests and questionnaires are used to assess patients' mobility and function. Participants will have physical function assessed at ICU discharge and at 90 days, along with measurements of mobility level, frailty, length of ICU and hospital stay, mortality rates, disability, and activities of daily living. Data collection includes routine clinical information and mobilisation details documented during the ICU stay. The goal is to evaluate how mobilisation practices relate to patient recovery and long-term outcomes. The study is sponsored by the Medical University of Vienna and started in December 2025, with results expected by June 2027.

CONDITIONS

Brief Title

Dosage of Early Rehabilitation of ICU Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (≥ 18 years old) within 48 hours of ICU admission
  • Expected to stay more than 24 hours in the ICU
Not Eligible

You will not qualify if you...

  • Patients who receive end-of-life care at the time of screening
  • Patients whose treatment plans are still under discussion and/or not all team members are committed to full active treatment
  • Patients whose functional status is unlikely to be obtainable
  • Patients with language barriers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - Up to 48 hours after ICU admission

Participants are screened for eligibility to participate in the trial.

1 initial assessment (in ICU)

Monitoring

Duration - Up to 28 days or until ICU discharge

Participants are observed during their ICU stay, with routine clinical data and mobilisation data collected to assess the variety and dosage of mobilisation practices.

Daily data collection during ICU stay

Long-term Monitoring

Duration - Up to 90 days after ICU admission

Participants undergo functional tests and complete questionnaires to evaluate physical function, frailty, mobility, and activities of daily living after ICU discharge.

Assessments at ICU discharge and at Day 90

Trial Site Locations

Total: 1 location

1

Medical University of Vienna

Vienna, State of Vienna, Austria, 1090

Actively Recruiting

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Research Team

V

Vera Karner, MSc

S

Stefan J Schaller, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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