Benefit of Sleep Quality Monitoring by EEG in ICU
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: EEG monitoring.
- Who it may be relevant to
- Registry conditions: Respiratory Failure. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Benefit of the Sleep Quality Assessment Using Electroencephalographic Monitoring in Critically Ill Patients
Overview
The goal of this observational study is to learn about the benefit of monitoring sleep quality using EEG in patients hospitalized in critical care unit for acute respiratory failure. The main question it aims to answer is: • Does EEG monitoring improve sleep quality assessment in critically ill patients with acute respiratory failure compared to nurse sleep quality assessment? Participants hospitalized in critical care unit for acute respiratory failure will have their sleep quality assessed by both EEG monitoring and nurse evaluation during their stay in critical care unit.
Interventions
- Other EEG monitoring
Participants will have their sleep quality assessed by both EEG monitoring and nurse evaluation during their stay in critical care unit.
Primary outcome measures
- sleep stage [Time frame: through study completion, an average of 7 days]
Secondary outcome measures (4)
- total sleep time [Time frame: periprocedurally]
- sleep quality [Time frame: through study completion, an average of 7 days]
- anxiety [Time frame: through study completion, an average of 7 days]
- respiratory assessment [Time frame: through study completion, an average of 7 days]
Eligibility criteria
Inclusion criteria
- Adults
- Acute respiratory failure with non-invasive ventilation or high-flow oxygenotherapy hospitalized in critical care unit
- Conscious
- Insurance coverage
- Consent to participate
Exclusion criteria
- pregnancy
- cutaneous lesion on the scalp
- guardianship
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
France · 1 center
- CHU de ROUEN — Rouen
Identifiers
NCT: NCT07522450 · 2025/0321/HP