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Contribution of the intensive care unit environment to sleep disruption in healthy subjects

Contribution of the intensive care unit environment to sleep disruption in healthy subjects - Sleep ICU healthy subjects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43235
Enrollment
10
Registered
2016-12-14
Start date
2016-12-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

slaapstoornissen Disturbed sleep sleep continuity

Interventions

Environmental factors
Intensive Care Unit
Sleep

Sponsors

Philips
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Healthy volunteers (nurses/doctors (in training)) not currently at work in the ICU Capable of understanding and speaking Dutch Normal hearing

Exclusion criteria

Exclusion criteria: Pre-existing history or treatment of sleep pathology Sleep promoting medication Alcohol addiction or illicit drug abuse

Design outcomes

Primary

MeasureTime frame
To determine the quality, quantity and distribution of sleep in healthy subjects in different environments. Sleep-related parameters (using EEG: Rechtschaffen & Kales (R&K) manual scoring) • Number of arousals (and awakenings) per hour • Total sleep time (any sleep stage other than awake, derived from EEG) • Sleep efficiency • Sleep continuity

Secondary

MeasureTime frame
To investigate the correlation between stressors present in the ICU environment and continuity of sleep, in healthy subjects. Percentage of arousals caused by sound • Correlation between sleep continuity and environmental parameters Environmental parameters: • Sound levels (decibel and amplitude of spectral components) • Reverberation time • Light levels (Lux) • Light frequencies • Temperature (degrees Celsius

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)