Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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