Clinical trial Recruiting at 1 site Observational Ages 18 and up

Finding the right amount of early rehabilitation for ICU patients

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

Run by Medical University of Vienna · NCT06960642 · Data updated 2026-11-12

This project will collect routine ICU data from adults to see if different amounts and types of early rehabilitation lead to better physical function and quality of life.

More Critical Illness trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment6000 (estimated)
SponsorMedical University of Vienna
Academic / other
Locations1 site (Vienna, State of Vienna)
StatusRecruiting
StartedDecember 14, 2025
Main results expectedMarch 2027
Study endsJune 2027
Registry record updatedFebruary 20, 2026
Trial IDNCT06960642 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (age 18 or older) admitted to a participating ICU within 48 hours who are expected to remain in the ICU more than 24 hours and whose functional status can be documented.

Probably not a fit

Patients receiving end-of-life care, those without reliable functional status data, or those with language barriers or undecided treatment plans may be excluded and are unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multinational observational project will record how ICUs worldwide provide early mobilisation and rehabilitation to adult patients. No new treatments are given; researchers will standardize and collect routine clinical data, established physical tests, and questionnaires from over 6,000 patients across at least 200 intensive care units. They will analyze how the 'dose' and type of mobilisation, plus patients' pre-hospital functional status and use of invasive ventilation, relate to outcomes such as physical function, functional status, and quality of life. Each patient is followed for 90 days and the total study runs about 21 months to compare real-world practices and outcomes.

Why it matters

Potential benefit: If successful, the findings could guide clinicians on how much and what kinds of early mobilisation best improve recovery, independence, and quality of life after an ICU stay.

How similar studies have gone: Smaller studies have shown that early mobilisation can improve physical outcomes and shorten ventilation and ICU stays, but large multinational data on optimal mobilisation 'dosage' are still lacking.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • Medical University of Vienna
    Vienna, State of Vienna, Austria
    Recruiting

Study contacts

  • Principal investigator: Stefan J Schaller, MD — Medical University of Vienna
  • Study coordinator: Vera Karner, MSc
  • Email: erupt@muv.ac.at
  • Phone: +4314040041020

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.