Transcranial Magnetic Stimulation for BECTS (TMS4BECTS)
Primary Purpose
Benign Epilepsy With Centrotemporal Spikes, Language Problems, Learning Disorders
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Active rTMS
Sham rTMS
Sponsored by
About this trial
This is an interventional basic science trial for Benign Epilepsy With Centrotemporal Spikes focused on measuring Transcranial Magnetic Stimulation (TMS), Electroencephalogram (EEG), Children, Pediatric, Interictal Epileptiform Discharges, Brain connectivity
Eligibility Criteria
Inclusion Criteria:
- A diagnosis of Benign Epilepsy with Centrotemporal Spikes (BECTS), sometimes called Rolandic Epilepsy. Diagnosis will be based on a history of a focal motor seizure (affecting the face or causing hypersalivation) or a history of a seizure out of sleep AND an EEG with unilateral or bilateral centrotemporal spike waves.
- English-speaking
Exclusion Criteria:
- History of prematurity < 35 weeks gestational age;
- History of serious neurologic problems (i.e. history of other seizure disorder other than simple febrile seizure, head trauma with prolonged loss of consciousness, cerebrovascular accident or neuro-inflammatory disease)
- Focal deficits on neurologic exam
- History of abnormal MRI (with clear gray or white matter abnormality)
Sites / Locations
- Stanford University School of MedicineRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Children with BECTS
Arm Description
Children will receive sham and active rTMS on 2 separate study visits separated by at least 1 week.
Outcomes
Primary Outcome Measures
Interictal Epileptiform Discharge (IED) Frequency
We will count the number of IEDs/minute before and after application of active rTMS as well as before and after sham rTMS. We will compare the change in IEDs induced by the active and sham stimulation.
Secondary Outcome Measures
Change in Brain Connectivity
We will measure brain connectivity before and after application of active rTMS as well as before and after sham rTMS. We will compare the change in connectivity induced by the active and sham stimulation. In particular, we will look at how connectivity changes between the motor cortex and language regions of the brain.
Full Information
NCT ID
NCT04325282
First Posted
March 25, 2020
Last Updated
February 15, 2023
Sponsor
Stanford University
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS)
1. Study Identification
Unique Protocol Identification Number
NCT04325282
Brief Title
Transcranial Magnetic Stimulation for BECTS
Acronym
TMS4BECTS
Official Title
Impact of Repetitive Transcranial Magnetic Stimulation (TMS) on Spike Frequency and Brain Connectivity in Children With Benign Epilepsy With Centrotemporal Spike (BECTS)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 28, 2020 (Actual)
Primary Completion Date
October 2024 (Anticipated)
Study Completion Date
October 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
National Institute of Neurological Disorders and Stroke (NINDS)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Benign epilepsy with centrotemporal spikes (BECTS) is the most common pediatric epilepsy syndrome. Affected children typically have a mild seizure disorder, but yet have moderate difficulties with language, learning and attention that impact quality of life more than the seizures. Separate from the seizures, these children have very frequent abnormal activity in their brain known as interictal epileptiform discharges (IEDs, or spikes), which physicians currently do not treat. These IEDs arise near the motor cortex, a region in the brain that controls movement.
In this study, the investigators will use a form of non-invasive brain stimulation called transcranial magnetic stimulation (TMS) to determine the impact of IEDs on brain regions important for language to investigate: (1) if treatment of IEDs could improve language; and (2) if brain stimulation may be a treatment option for children with epilepsy.
Participating children will wear electroencephalogram (EEG) caps to measure brain activity. The investigators will use TMS to stimulate the brain region where the IEDs originate to measure how this region is connected to other brain regions. Children will then receive a special form of TMS called repetitive TMS (rTMS) that briefly reduces brain excitability. The study will measure if IEDs decrease and if brain connectivity changes after rTMS is applied.
The investigators hypothesize that the IEDs cause language problems by increasing connectivity between the motor cortex and language regions. The investigators further hypothesize that rTMS will reduce the frequency of IEDs and also reduce connectivity between the motor and language region
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Epilepsy With Centrotemporal Spikes, Language Problems, Learning Disorders
Keywords
Transcranial Magnetic Stimulation (TMS), Electroencephalogram (EEG), Children, Pediatric, Interictal Epileptiform Discharges, Brain connectivity
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Children will receive active repetitive TMS (rTMS) on one day and sham stimulation on a second day. The order of stimulation will be randomized on a per-participant basis.
Children and parents/guardians will not be told if they are receiving sham or inhibitory rTMS on a given day. The research team will know at the time of stimulation, however, as they will have to choose which coil to use. The TMS-EEG files will be coded and the team member analyzing the files for change in IED (spike) frequency and change in connectivity will be blinded to condition.
Masking
None (Open Label)
Allocation
N/A
Enrollment
36 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Children with BECTS
Arm Type
Experimental
Arm Description
Children will receive sham and active rTMS on 2 separate study visits separated by at least 1 week.
Intervention Type
Device
Intervention Name(s)
Active rTMS
Intervention Description
1Hz rTMS delivered for 15-20 minutes
Intervention Type
Device
Intervention Name(s)
Sham rTMS
Intervention Description
sham rTMS delivered for 15-20 minutes
Primary Outcome Measure Information:
Title
Interictal Epileptiform Discharge (IED) Frequency
Description
We will count the number of IEDs/minute before and after application of active rTMS as well as before and after sham rTMS. We will compare the change in IEDs induced by the active and sham stimulation.
Time Frame
Before and after intervention (approximately 4 hours/visit on 2 study days one week apart)
Secondary Outcome Measure Information:
Title
Change in Brain Connectivity
Description
We will measure brain connectivity before and after application of active rTMS as well as before and after sham rTMS. We will compare the change in connectivity induced by the active and sham stimulation. In particular, we will look at how connectivity changes between the motor cortex and language regions of the brain.
Time Frame
Before and after intervention (approximately 4 hours/visit on 2 study days one week apart)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
A diagnosis of Benign Epilepsy with Centrotemporal Spikes (BECTS), sometimes called Rolandic Epilepsy. Diagnosis will be based on a history of a focal motor seizure (affecting the face or causing hypersalivation) or a history of a seizure out of sleep AND an EEG with unilateral or bilateral centrotemporal spike waves.
English-speaking
Exclusion Criteria:
History of prematurity < 35 weeks gestational age;
History of serious neurologic problems (i.e. history of other seizure disorder other than simple febrile seizure, head trauma with prolonged loss of consciousness, cerebrovascular accident or neuro-inflammatory disease)
Focal deficits on neurologic exam
History of abnormal MRI (with clear gray or white matter abnormality)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fiona M Baumer, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fiona M Baumer, MD
Phone
650-721-5889
Email
fbaumer@stanford.edu
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No current plan.
Citations:
PubMed Identifier
32142025
Citation
Baumer FM, Pfeifer K, Fogarty A, Pena-Solorzano D, Rolle CE, Wallace JL, Rotenberg A, Fisher RS. Cortical Excitability, Synaptic Plasticity, and Cognition in Benign Epilepsy With Centrotemporal Spikes: A Pilot TMS-EMG-EEG Study. J Clin Neurophysiol. 2020 Mar;37(2):170-180. doi: 10.1097/WNP.0000000000000662.
Results Reference
background
PubMed Identifier
31942753
Citation
Mishra A, Maiti R, Mishra BR, Jena M, Srinivasan A. Effect of Repetitive Transcranial Magnetic Stimulation on Seizure Frequency and Epileptiform Discharges in Drug-Resistant Epilepsy: A Meta-Analysis. J Clin Neurol. 2020 Jan;16(1):9-18. doi: 10.3988/jcn.2020.16.1.9.
Results Reference
background
PubMed Identifier
27513825
Citation
Chen R, Spencer DC, Weston J, Nolan SJ. Transcranial magnetic stimulation for the treatment of epilepsy. Cochrane Database Syst Rev. 2016 Aug 11;(8):CD011025. doi: 10.1002/14651858.CD011025.pub2.
Results Reference
background
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Transcranial Magnetic Stimulation for BECTS
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