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Clinical Trials in Austria / NCT06960642
Recruiting Observational

Dosage of Early Rehabilitation of ICU Patients

NCT06960642 · tracked via the Priya Life Science Austria tracker
Phase
Observational
Started
2025-12-14
Last updated
2026-02-20

Condition(s) studied

Critical Care, Intensive CareCritical IllnessPhysiotherapyEarly AmbulationInterprofessional Team Collaboration

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (≥ 18 years old) within 48 hours of ICU admission * Expected to stay \> 24 hours in the ICU Exclusion Criteria: * 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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Medical University of Vienna Vienna State of Vienna Recruiting

More Medical University of Vienna trials in Austria

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06960642 on ClinicalTrials.gov ↗ ← All trials in Austria