Evaluation of Rehabilitation Practices in the Intensive Care Unit (REHALITE)

September 23, 2025 updated by: French Society for Intensive Care

Evaluation of Rehabilitation Practices in Patients Undergoing Invasive Mechanical Ventilation in French-speaking Critical Care Units

This observational study aims to describe the number of rehabilitation procedures performed per patient during their stay in French-speaking adult intensive care units undergoing invasive mechanical ventilation (average rehabilitation ratio). The study aims to determine the actual rehabilitation ratio, i.e. the number of rehabilitation procedures divided by the number of critical care hospital days (censored at day 28 from the start of invasive mechanical ventilation), provided to patients undergoing invasive mechanical ventilation. The rehabilitation procedure will remain the same, and ICU teams will only record the number of procedures performed per day.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

1000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Guillaume FOSSAT, Physiotherapist Msc, PhD Student
  • Phone Number: +331 45 86 74 00
  • Email: secretariat@srlf.org

Study Locations

  • France
      • Paris, France
        • Recruiting
        • SRLF

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adult patients undergoing mechanical ventilation (MV) via an endotracheal tube for less than five days, in French-speaking intensive care units in three countries (France, Belgium and Switzerland), in whom MV is scheduled to last more than 48 hours.

Description

Inclusion criteria:

  • Foreseeable invasive ventilation lasting more than 48 hours.
  • Included within the first five days of an intensive care stay.

Exclusion criteria:

  • Participation in an interventional study on early rehabilitation in the ICU
  • Moribund patient
  • Pregnant or breastfeeding woman
  • A person deprived of liberty by court order
  • Not being affiliated to a social security scheme

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rehabilitation Ratio
Time Frame: On Day 28 of study participation
Number of rehabilitation procedures per day divided by the number of ICU days (censored at D28 from the start of invasive mechanical ventilation)
On Day 28 of study participation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

French Society for Intensive Care

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 17, 2025

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

May 5, 2025

First Submitted That Met QC Criteria

May 12, 2025

First Posted (Actual)

May 13, 2025

Study Record Updates

Last Update Posted (Estimated)

September 24, 2025

Last Update Submitted That Met QC Criteria

September 23, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • SRLF-012025
  • 2025-A00025-44 (Other Identifier: IDRCB)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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