High-frequency neural activity and human cognition: past, present and possible future of intracranial EEG research.
Jean-Philippe Lachaux, Nikolai Axmacher, Florian Mormann...
https://pubmed.ncbi.nlm.nih.gov/22750156Actively Recruiting
Led by University Hospital, Grenoble · Updated on 2024-03-19
200
Participants Needed
4
Research Sites
130 weeks
Total Duration
Researchers are studying patients with refractory or focal epilepsy who undergo pre-surgical evaluation using Stereoelectroencephalography (SEEG). The goal is to create a detailed brain atlas of human cognition by collecting brain recordings taken during cognitive tasks performed as part of routine clinical care. This atlas will provide high temporal and spatial resolution data to better understand how epilepsy and epilepsy surgery affect cognitive functions. Participants will have intracerebral electrodes implanted as part of their invasive SEEG assessment to locate epileptogenic zones and evaluate cognitive risks before surgery. During this procedure, brain activity is recorded while patients perform cognitive tasks. This study uses Dynamic Spectral Imaging (ISD) to map gamma oscillations in the brain, which are linked to complex cognitive functions. Behavioral and neuropsychological data may also be collected after surgery. During the study, participants complete cognitive tasks while SEEG signals are visually and quantitatively analyzed over about three weeks. Researchers measure brain activity through functional mapping and record composite behavioral data. The study monitors patients’ intellectual capacity to comply with cognitive testing and collects detailed brain function data to improve understanding of epilepsy's impact on cognition. Participation lasts through the clinical evaluation and data collection periods.
CONDITIONS
Atlas of Human Cognition by SEEG (MAPCOG-SEEG)
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 3 weeks
Participants undergo invasive exploration by implantation of intracerebral electrodes during SEEG to evaluate epileptogenic zones and cognitive functions through brain mapping.
Multiple visits for SEEG recording and functional brain mapping
Duration - Up to 3 weeks
Participants' behavioral and neuropsychological data are collected postsurgically to assess cognitive outcomes.
Visits as needed for behavioral and neuropsychological assessments
Total: 4 locations
1
University Hospital, Grenoble
Grenoble, France, 38043
Actively Recruiting
2
CHRU Nancy
Nancy, France
Actively Recruiting
3
Hôpital Ste Anne
Paris, France, 75014
Actively Recruiting
4
CHU Rennes
Rennes, France
Actively Recruiting
P
Philippe Kahane, MD/PhD
M
Marcela Perrone-Bertolotti, PhD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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