Actively Recruiting
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
Eligibility Criteria
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
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
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Your Study Journey
Duration - Up to 48 hours after ICU admission
Participants are screened for eligibility to participate in the trial.
1 initial assessment (in ICU)
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
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
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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