Routine cardiorespiratory and sleep monitoring in an epilepsy monitoring unit

Not Applicable

• Conditions: epilepsy; non-epileptic seizures; psychogenic non-epileptic seizures (PNES); Neurological - Epilepsy

• Registration Number: ACTRN12621000923864
• Lead Sponsor: Alfred Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-07-15
• Last Update Posted: 21 July 2021

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 1200

Inclusion Criteria

•Can provide personally signed and dated informed consent to participate in the study before completing any study related procedures.
•Male or female (aged 18 years or older).
•Possible diagnosis of epilepsy or non-epileptic events and admitted for inpatient video-EEG monitoring.

Exclusion Criteria

•Patients who are on CPAP treatment during the monitoring period.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
T0 analyse cardiac, respiratory, sleep polysomnography physiological data during (ictal) and around (interictal) seizures for seizure detection, using machine learning models. Various features including unprocessed data (e.g., raw electrocardiogram signals) and descriptive data (e.g., median heart rate) data be explored; all physiological variables will be assessed as a composite outcome.[This is a cross-sectional study. Data collected during the final day of admission of video-EEG monitoring where polysomnography has been applied, will be analysed.]