Actively Recruiting

Age: 18Years +
All Genders
NCT07251530

Communication Enhancement Among Ventilated Patients in Intensive Care

Led by University Hospital, Tours · Updated on 2026-05-04

60

Participants Needed

3

Research Sites

62 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Intensive care is a unit that admits ventilated patients. Hospitalization is extremely challenging for these patients. Their vital prognosis is at stake, and they often have difficulty moving due to pain, edema, neuromyopathy, or the presence of monitoring cables. They are also hindered in their communication: they cannot speak because of the presence of the intubation tube between their vocal cords or the tracheostomy cannula with the inflated cuff. Every day, in each intensive care unit, about 50% of ventilated patients are conscious and face communication difficulties. They describe this difficulty as a "nightmare." This leads to challenges in care management and increases the anxiety caused by hospitalization in the intensive care unit. A large proportion of patients will develop post-intensive care syndrome. The tools currently used are not efficient. Moreover, many patients have comprehension difficulties due to the medications administered to them (sedatives) or due to the initial or secondary pathologies related to their hospitalization (confusional syndrome, ICU delirium). Our objective is to implement an adapted and personalized communication tool for ventilated patients in intensive care.

CONDITIONS

Official Title

Communication Enhancement Among Ventilated Patients in Intensive Care

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Intubated ventilated ICU patient
  • Hospitalized patient with an inflated cuff tracheostomy
  • Conscious patient, able to open and close eyes on demand
  • Patient aged 18 years or older
  • French speaking
Not Eligible

You will not qualify if you...

  • Patient with uncorrected visual impairment or hearing deficiency
  • Known guardianship or trusteeship at the time of inclusion
  • Known pregnant women at the time of inclusion and lactating patients
  • Opposed to the processing of personal data

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Intensive care, Hospital, Le MANS

Le Mans, France

Not Yet Recruiting

2

Intensive care, University Hospital, Orléans

Orléans, France

Not Yet Recruiting

3

Intensive care, University Hospital

Tours, France, 37000

Actively Recruiting

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Research Team

L

Laetitia BODET-CONTENTIN, Doctor

CONTACT

A

Adrien LOCICIRO, nurse

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

0

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