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Search / Trial NCT06973746

Effect of the "Sitting Out of Bed in an Arm-chair Position" in ICU on Functional Recovery Among Ventilated Patients

Launched by CENTRE HOSPITALIER RÉGIONAL D'ORLÉANS · May 7, 2025

Trial Information

Current as of July 23, 2025

Recruiting

Keywords

Mechanical Ventilation Icu Acquired Weakness Arm Chair Sitting Early Mobility

ClinConnect Summary

This clinical trial is studying whether sitting patients in an armchair in the intensive care unit (ICU) can help them recover better than if they are only sitting in bed. The trial focuses on patients who are on a ventilator and may experience weakness after being in the ICU. By encouraging patients to sit in a chair, the researchers hope to improve their breathing and strength, which could lead to a faster recovery.

To participate in the trial, patients must be over 18 years old, have been on a ventilator for at least 24 hours, and be awake and alert enough to participate. They should also not have any serious medical issues that would prevent them from sitting in a chair. If eligible, participants will be assigned to either sit in an armchair or remain in bed, and their progress will be monitored. This study aims to provide more evidence on the benefits of early mobilization techniques in the ICU, which could ultimately help many patients recover more effectively.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Patient \> 18 years old
  • 2. Patient on invasive mechanical ventilation for more than 24 hours
  • 3. Patient in recovery phase with a RASS score greater than "-3" for more than 12 hours
  • 4. Stay expected to last 72 hours
  • 5. Patient has never been placed in a chair during this hospitalization in intensive care.
  • 6. Fragility score \< 6, during the month preceding admission to intensive care
  • 7. Patient (or support person/relative if patient is unable to participate) who has agreed to take part in the study.
  • Exclusion Criteria:
  • 1. Patient with an absolute and non-resolving contraindication to chair positioning
  • 1. Fracture or orthopedic disorder contraindicating mobilization out of bed
  • 2. Obesity with body mass index greater than 45 kg/cm2
  • 3. Sacral eschar stage greater than 2
  • 2. Patient using a wheelchair for mobility (i.e. paraplegic patient or patient with progressive neurological pathology).
  • 3. Patient treated with veno-venous or veno-arterial ECMO at the time of screening.
  • 4. Moribund patient
  • 5. Encephalic death
  • 6. Acute polyradiculoneuritis (Guillain-Barré syndrome)
  • 7. Myasthenia
  • 8. Patient treated by continuous hemodialysis or hemofiltration for more than 72 hours following the onset of awakening.
  • 9. Complete transmetatarsal or higher amputation of one or both lower limbs.
  • 10. Protected person (under guardianship or curatorship)
  • 11. Person under court protection
  • 12. Person not affiliated to a social security scheme
  • 13. Pregnant or breast-feeding woman
  • 14. Patient already included in the study
  • 15. Patient taking part in an interventional clinical study, the aim of which is to show an improvement in functional level on discharge from the intensive care unit or which focuses on the theme of early rehabilitation in the intensive care unit.

About Centre Hospitalier Régional D'orléans

The Centre Hospitalier Régional d'Orléans is a leading healthcare institution dedicated to advancing medical research and improving patient care through innovative clinical trials. Located in Orléans, France, the center is committed to fostering a collaborative environment that integrates clinical expertise with cutting-edge research methodologies. By facilitating multidisciplinary studies across various therapeutic areas, the Centre Hospitalier Régional d'Orléans aims to enhance treatment protocols and contribute to the global body of medical knowledge, ultimately benefiting patients and the healthcare community at large.

Locations

Suresnes, , France

Dijon, , France

Tours, , France

Clermont Ferrand, , France

Dax, , France

Le Mans, , France

Le Coudray, , France

Belfort, , France

Orléans, Centre Val De Loire, France

Mont De Marsan, , France

Patients applied

0 patients applied

Trial Officials

Guillaume FOSSAT

Principal Investigator

CHU Orléans

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported