Neural Basis of Cognition

Sponsor
Duke University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05132543
Collaborator
(none)
50
1
70.4

Study Details

Study Description

Brief Summary

The overall purpose of this study is to better understand human cognition and human epilepsy by working with patients undergoing clinical treatment for pharmacologically resistant epilepsy. The investigators will investigate human cognition by conducting controlled experiments that focus on sensory, motor, and cognitive phenomena such as sensory processing, memory, and language. The investigators will also examine the neural underpinnings of epilepsy during both sleep and wakefulness to better understand both the foundations of epilepsy and how epilepsy affects cognition. The investigators hope to use these data to have a better understanding of cognition, epilepsy, and how the two interact. This will potentially lead to better markers for seizure onsets as well as epilepsy more generally. For this research, the investigators will use μECoG arrays manufactured by commercial partners. These arrays have passed all major ISO 10993 bio-compatibility tests. Based on this characterization and use in the intraoperative setting (limited duration and supervised usage), these devices pose a minimal risk to participants. Data will be analyzed and protected using the Duke SSRI protected research data network.

Condition or Disease Intervention/Treatment Phase
  • Device: High density micro-electrocorticography for neural speech prothesis
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Studying Human Cognition and Neurological Disorders Using µECoG Electrodes
Actual Study Start Date :
Nov 1, 2016
Anticipated Primary Completion Date :
Sep 15, 2022
Anticipated Study Completion Date :
Sep 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Wireless µECoG Prosthesis for Speech

Device: High density micro-electrocorticography for neural speech prothesis
ECoG electrodes are thin, high-density, flexible electrode arrays used for recording electrophysiological signals from the brain.

Outcome Measures

Primary Outcome Measures

  1. Evoked signal-to-noise analysis human brain. [Intraoperative data collection period, 20 minutes]

    This study will compare the neural response sensitivity of intraoperative µECoG recording to those of in-unit recordings with macro-ECoG and SEEG. The strength and reliability of the high gamma (HG) response are critical for speech decoding algorithms. For all recordings, the HG power modulation ratio over baseline during speech perception and production will be measured and compared with non-parametric statistical tests.

  2. Percentage of phoneme decoding accuracy as measured by linear decoding model [Intraoperative data collection period, 20 minutes]

  3. Number of HG power modulation as measured by signal power. [Intraoperative data collection period, 20 minutes]

  4. Number of kriging resolution as measured by signal power. [Intraoperative data collection period, 20 minutes]

Secondary Outcome Measures

  1. Number of serious adverse events as measured by medical record review [Implantation to Three-months follow-up]

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Potential subjects will come from adult and pediatric patients (between the ages of 12 and 18) undergoing surgery for the treatment of pharmacologically resistant epilepsy, brain tumor resection, brain mass resection, or deep brain stimulation (DBS) for the first time

  • Proficient English speakers

  • No Major cognitive impairment

Exclusion Criteria:
  • Previous DBS procedure

  • Subject unable to consent to study

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Duke University

Investigators

  • Principal Investigator: Gregory B Cogan, PhD, Duke University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Duke University
ClinicalTrials.gov Identifier:
NCT05132543
Other Study ID Numbers:
  • Pro00072892
First Posted:
Nov 24, 2021
Last Update Posted:
Dec 6, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 6, 2021