Cognitive Assessment in Excessive Daytime Sleepiness: Electrophysiological Study.

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03446066

Enrollment

Registered

2018-02-26

Start date

2015-01-12

Completion date

2017-12-23

Last updated

2018-02-26

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

Conditions

Cognitive Impairment

Brief summary

Cognition was assessed using Minimental state examination (MMSE), Trail making tests A and B (TMT) tests, P300 and quantitative electroencephalography (QEEG) sleepiness was assessed using Epworth Sleepiness Scale (ESS), Karolinska sleepiness scale (KSS) and QEEG also polysomnography (PSG) was done for all participated subjects

Detailed description

\*The study is a case control study included 40 subjects, divided into 20 cases suffering from Excessive daytime sleepiness and 20 healthy control group. all participants were subjected to: 1. Careful history taking and Complete neurological examination. 2. Initial assessment of cognition and sleepiness by two scales which were done once before sleep: Epworth Sleepiness Scale (ESS) and Minimental state examination (MMSE) 3. Scales and neurophysiological studies done before and after sleep:Karolinska sleepiness scale (KSS), Trail making tests A and B (TMT), P300, and QEEG 4. Polysomnography (PSG) * EEG was recorded for 20 minutes duration before and after sleep recording. In each EEG recording, alpha attenuation test (AAT) was done after 10 minutes of recording basal resting EEG, then the absolute power of 5 electrodes (CZ, T3, T4, T5, T6,) were studied in the following frequency bands: delta (0.5-3Hz), theta (4-7 Hz) and also the absolute power of (O1, O2) were studied in delta, theta and alpha (8-12 Hz) bands.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

31 Years to 58 Years

Inclusion criteria

* The age ranges from 18 to 60 years. The age of all included subjects was 31-58 yrs old. * The body mass index (BMI) range is 24.97-39.06 kg/m2 in patients and 23.40-43.0 kg/m2 in control group. * Patients suffering from excessive daytime sleepiness symptoms according to the International Classification of Sleep Disorders definitions.

Exclusion criteria

* Patients suffering from EDS secondary to any sleep disorder other than sleep disordered breathing. * Chronic debilitating disease as diabetes mellitus , hypertension or hyper- or hypo-thyroidism. * Medications that could affect attention or vigilance as Benzodizipines, anti-psychotics or anti-epileptics.

Design outcomes

Primary

Measure	Time frame	Description
change in Quantitative electroencephalography (QEEG) and P300 results from before to after single night sleep record in patients with excessive daytime sleepiness (EDS)	1 year	the results of QEEG and P300 in patients with EDS before and after sleep

Secondary

Measure	Time frame	Description
potential integration of quantitative EEG and P300 as diagnostic tools for cognition and EDS.	1year	usage of electrophysiological tools for diagnosis of cognitive affection and sleepiness in EDS patients

Outcome results