Measuring quality of sleep in critically ill patients in the ICU: A pilot study

Measuring quality of sleep in critically ill patients in the ICU: A pilot study - Measuring quality of sleep in the ICU

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON36890

Enrollment

Registered

2012-07-23

Start date

2012-07-23

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

delirium quality of sleep

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Non-surgical ICU patients. Expected duration of ICU-stay > 24 hours. Written informed consent given by the patient according to the regulations.

Exclusion criteria

Exclusion criteria: Life expectancy of 72 hours Blindness or severe visual impairment Known or proven neuropathology

Design outcomes

Primary

Measure	Time frame
Main study parameters/endpoints: The main study parameters will be the total sleep time (TST), percentage of TST spent in Rapid Eye Movement (REM) sleep, percentage of TST spent in stage 1-2 and stage 3-4 Non REM sleep, the number of awakenings and the number of arousals.	—

Secondary

Measure	Time frame
Best fit coefficients of circadian rhythm models are compared between melatonin assay and CBT. Incidence of delirium is determined through the Confusion Assessment Method for the ICU (CAM-ICU) observation scale.	—

Countries

Netherlands

Outcome results