Actively Recruiting
Spatial Scene Recognition Memory in Epilepsy Surgery
Led by University of California, Davis · Updated on 2026-05-12
620
Participants Needed
2
Research Sites
312 weeks
Total Duration
On this page
Sponsors
U
University of California, Davis
Lead Sponsor
E
Emory University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study investigates the anatomical and physiological basis of spatial scene recognition memory in patients with temporal lobe epilepsy and temporal lobe lesions. Standard neuropsychological tests are insensitive to important memory deficits experienced by patients, particularly in spatial/scene memory, recollective experience, and familiarity processing. Using a validated virtual tour paradigm, the study examines how familiarity-based recognition and recall of spatial scenes relate to specific brain structures. In Aim I, a large cohort of patients with varied temporal lobe lesions at Emory University undergoes the virtual tour task with voxel-based lesion-symptom mapping to localize necessary brain regions. In Aim II, scalp event-related potentials and eye tracking in healthy participants at UC Davis characterize the temporal dynamics and lateralization of scene recognition. In Aim III, intracranial EEG recordings (including local field potentials and single-unit activity) in epilepsy surgery patients at UC Davis determine the precise network dynamics underlying spatial scene familiarity and recall. The long-term goal is to improve the prediction and prevention of cognitive morbidity from epilepsy surgery by providing a more complete model of spatial recognition memory circuits.
CONDITIONS
Official Title
Spatial Scene Recognition Memory in Epilepsy Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosis of focal epilepsy or temporal lobe lesion for Aims I and III; patients undergoing evaluation for or having had epilepsy surgery
- Healthy adult participants for Aim II
- Full-Scale IQ of 70 or higher
- Sufficient English proficiency to understand and complete tasks
- Enrolled in or eligible for Emory University epilepsy surgery research registry for Aim I
- Undergoing clinically indicated stereoelectroencephalography (SEEG) at UC Davis Medical Center for Aim III
- Able to provide informed consent (or prior consent for Aim I retrospective participants)
You will not qualify if you...
- Full-Scale IQ below 70
- Inability to provide informed consent
- Age over 55 years for Aim III
- History of neurological or psychiatric disorder for Aim II as per protocol
AI-Screening
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Trial Site Locations
Total: 2 locations
1
UC Davis Medical Center
Sacramento, California, United States, 95817
Actively Recruiting
2
Emory University Hospital
Atlanta, Georgia, United States, 30322
Actively Recruiting
Research Team
N
Nigel P Pedersen, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
3
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