Actively Recruiting
Dosage of Early Rehabilitation of ICU Patients
Led by Medical University of Vienna · Updated on 2026-02-20
6000
Participants Needed
1
Research Sites
76 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
Rehabilitation already begins in the intensive care unit (ICU) to maintain or restore the functional capacity of ICU patients and to counteract the long-term effects of intensive care treatment. Mobilisation is an important component. The aim of this multinational observational study is to record and evaluate the different mobilisation practices for ICU patients worldwide. The investigators want to find out which forms of mobilisation in intensive care patients achieve the best results in terms of physical function, functional status and quality of life. The goal is to recruit over 6,000 patients internationally. No interventions will be carried out, only routine clinical data will be documented and standardised and already established physical tests and questionnaires will be used.
CONDITIONS
Official 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 > 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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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
CONTACT
S
Stefan J Schaller, MD
CONTACT
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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