An inception cohort study to determine feasibility of measuring sleep, proportion of patients with a new sleep disorder, and sleep changes over time during critical illness and recovery

Not Applicable

Completed

• Conditions: Critical illness; Sleep disorder; Neurological - Other neurological disorders

• Registration Number: ACTRN12619000181101
• Lead Sponsor: Royal Melbourne Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-02-07
• Study Completion: 2020-06-16
• Last Update Posted: 20 June 2022

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 21

Inclusion Criteria

Critically-ill patients admitted to ICU
Aged >18 years
Treated in RMH ICU for >/= 5 calendar days total
Expected to remain in ICU for at least one more night

Exclusion Criteria

Patients with a previously diagnosed sleeping disorder
Patients with normal residence >50km from RMH
Patients unlikely to survive 3 months from the first study day in ICU
Patients unlikely to be discharged home within 3 months of the first study day in ICU
Patients receiving thiopentone to achieve 'EEG burst suppression'
Patients currently being treated for status epilepticus
Patients whose ICU admission was a planned admission post-elective surgery
Pregnancy
Patients who are unable to provide informed consent via self or MTDM
Patients who lack decision making capacity and are unable to identify a MTDM

Study & Design

• Study Type: Observational
• Study Design: Not specified