Actively Recruiting

Age: 18Years +
All Genders
ID07522450

Benefit of the Sleep Quality Assessment Using Electroencephalographic Monitoring in Critically Ill Patients

Led by University Hospital, Rouen · Updated on 2026-05-15

47

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the benefit of monitoring sleep quality using electroencephalographic (EEG) monitoring in adults hospitalized in critical care units for acute respiratory failure. It focuses on comparing EEG monitoring with nurse evaluations to see if EEG provides a better assessment of sleep quality in these critically ill patients. The study is observational and led by University Hospital, Rouen. Participants will have their sleep quality assessed during their stay in the critical care unit by both EEG monitoring and nurse evaluations. The study observes adults with acute respiratory failure receiving non-invasive ventilation or high-flow oxygen therapy. There are no treatment interventions as it is an observational study focused on monitoring and assessment. During the study, participants' sleep stages will be monitored for about 7 days on average. Researchers will also measure total sleep time, sleep quality, anxiety, and respiratory function during the same period. Participants provide consent and are monitored while hospitalized. The study does not involve additional treatments but collects data to better understand sleep quality assessment in critical care settings.

CONDITIONS

Brief Title

Benefit of Sleep Quality Monitoring by EEG in ICU

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults
  • Acute respiratory failure with non-invasive ventilation or high-flow oxygenotherapy hospitalized in critical care unit
  • Conscious
  • Insurance coverage
  • Consent to participate
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Cutaneous lesion on the scalp
  • Guardianship

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Approximately 7 days

Participants have their sleep quality assessed by EEG monitoring and nurse evaluation during their stay in the critical care unit.

Continuous monitoring during ICU stay

Trial Site Locations

Total: 1 location

1

CHU de ROUEN

Rouen, France, 76 031

Actively Recruiting

Loading map...

Research Team

M

Marie-Anne Melone, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

Similar Trials

A New Tool for Extubation Readiness in Mechanically Ventilat...

Ventilator Weaning

Actively Recruiting

7 locations

A Post Market Surveillance Study of the Hemovent Extracorpor...

Cardiac Failure

Actively Recruiting

4 locations

A Prospective Randomized Controlled Trial Comparing High-Flo...

Systolic Heart Failure

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here