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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05159609
Other study ID # 7796
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2020
Est. completion date August 31, 2021

Study information

Verified date December 2021
Source Cardiff and Vale University Health Board
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a single-centre pilot study of a non-invasive auditory stimulation during sleep in participants with temporal lobe epilepsy.


Description:

The primary objectives will be to pilot the use of home-based auditory stimulation during sleep in 10-20 participants with temporal lobe epilepsy using wireless devices.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date August 31, 2021
Est. primary completion date August 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: 1. Participant is willing and able to give informed consent 2. Participant diagnosed with temporal lobe epilepsy 3. Will have had fewer than three generalized tonic clonic seizures per month in the last three months 4. Will be taking 3 or fewer anti-seizure medications. 5. Will have access to a computer or cellphone with an internet connection Exclusion Criteria: 1. Abnormal hearing that cannot be corrected to normal overnight. 2. Abnormal vision that cannot be corrected to normal during the day. 3. Unwilling to abstain from caffeine, alcohol, daytime naps and extreme physical exercise in the 12 hours prior to the study. 4. Cannot read English 5. Engaged in night work in the previous 2 months 6. Any history of seizures triggered by music or sounds 7. Travelled across more than 2 time zones in the last 2 months 8. Prescribed/taking sleeping tablets other than clobazam 9. Cannabis use >4 joints/day.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Closed loop auditory stimulus
50ms of low volume pink noise delivered during slow wave sleep

Locations

Country Name City State
United Kingdom Cardiff and Vale UHW, Neurology department, ward C4, video-EEG monitoring unit Cardiff

Sponsors (1)

Lead Sponsor Collaborator
Cardiff and Vale University Health Board

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in EEG waveform amplitude Does the acoustic sound delivery alter EEG waveform amplitude of slow wave sleep 5 seconds after stimulus
Primary Change in Serial Reaction Time Task memory test Does the delivery of acoustic sounds alter post-sleep preformance on the above task Baseline and following day
Primary Change in Paired Associates Learning memory test Does the delivery of acoustic sounds alter post-sleep preformance on the above task Baseline and following day
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