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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03111290
Other study ID # 13-2710
Secondary ID 1R21NS0949881R01
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date January 2014
Est. completion date December 2024

Study information

Verified date February 2024
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: To investigate whether rhythmic direct electrical stimulation (DES) causes entrainment of endogenous neural oscillatory activity and whether such activity improve cognition. Participants: Drug-resistant epilepsy patients undergoing epilepsy surgery cortical mapping with continuous electrocorticography (ECoG) with intracranial electrodes. Procedures (methods): Rhythmic electrical stimulation will be delivered via intracranial electrodes during routine extra-operative cortical mapping. Long-term ECoG, Pre-stimulation ECoG, peri-stimulation ECoG, and post-stimulation ECoG data will be analyzed to assess for entrainment of neural oscillations.


Description:

The aim of this study is to characterize the entrainment of endogenous neural oscillatory activity using direct electrical stimulation (DES) of the brain and understand the effects on cognition. In this study, the investigators will apply rhythmic DES to patients who are undergoing routine DES for cortical mapping as a part of their epilepsy surgery evaluation with the aim of entraining cortical neural oscillations at specific frequencies relevant to cognitive processing and neuropsychiatric disease. The investigators hypothesize that rhythmic DES within a naturally occurring oscillatory frequency will cause entrainment at that frequency (e.g. 10Hz rhythmic DES will entrain a 10 Hz alpha oscillation). Also, the investigators posit that rhythmic DES at the theta (5Hz), alpha(10Hz), and gamma (50Hz) frequencies will cause enhancement of neural oscillations in the gamma band. The study follows a within-participant crossover design. Participants will perform one of the tasks described below and each task consists of multiple trials of varying difficulty. Stimulation will be applied concurrently through electrodes implanted for clinical determination of seizure focus. Equal number of stimulation and sham trials will be pseudo-randomly interleaved to get a balanced design (balanced across trial difficulty and trial type). The investigators will apply electrical stimulation in the form of pulse trains. The applied electrical stimulation intensity, duration and frequency follow the parameters used for clinical assessments of language and seizure focus and fall below the clinically approved limits. The investigators will measure participants performance on a simple working memory task during the above-described cortical electrical stimulation protocol. Alternately, participants can perform a face recognition task.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 30
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. History of medically intractable epilepsy 2. Capable of giving informed consent 3. Aged 18 - 80 years, either sex Exclusion Criteria: 1. Past or current history of other neurological illnesses including ischemic stroke, intracerebral hemorrhage, brain neoplasm. 2. Major systemic illness 3. Severe cognitive impairment defined as mini-mental state examination of less than 20 4. Severe psychiatric illness 5. Excessive use of alcohol or other substances

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Direct Cortical Stimulation
A train of periodic electrical pulses is delivered between two local electrodes implanted in the brain
Direct Cortical Stimulation Sham
Sham trials where no electric pulse is delivered

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill National Institute of Mental Health (NIMH), National Institute of Neurological Disorders and Stroke (NINDS)

References & Publications (1)

Alagapan S, Schmidt SL, Lefebvre J, Hadar E, Shin HW, Fr?hlich F. Modulation of Cortical Oscillations by Low-Frequency Direct Cortical Stimulation Is State-Dependent. PLoS Biol. 2016 Mar 29;14(3):e1002424. doi: 10.1371/journal.pbio.1002424. eCollection 2016 Mar. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Facial Recognition Task Performance - Accuracy Participants who consent will be administered this task. On a given trial, participants will be presented with images of two faces side-by-side. The faces will either match in terms of emotion category (e.g., 2 anger faces) or not (e.g., an anger face and a fear face). Faces presented together will always be of the same gender but different identities. Participants will be asked to determine whether the two faces presented depict the same emotion category. Participants will have 5 seconds to make the decision and indicate by pressing a key in the keyboard. Accuracy will be quantified in percent correct. 1 Hour
Other Facial Recognition Task Performance - Reaction Time Participants who consent will be administered this task. On a given trial, participants will be presented with images of two faces side-by-side. The faces will either match in terms of emotion category (e.g., 2 anger faces) or not (e.g., an anger face and a fear face). Faces presented together will always be of the same gender but different identities. Participants will be asked to determine whether the two faces presented depict the same emotion category. Participants will have 5 seconds to make the decision and indicate by pressing a key in the keyboard. Reaction times will be quantified in milliseconds. 1 Hour
Primary Working Memory Task Performance - Accuracy In this task, a sequence of items (alphabets or numerals) is presented followed by a delay. Following this, a single item which may or may not have been in the sequence is presented and the subject will be asked to indicate whether the item was in the previously presented sequence. A total of 150 trials will be performed with randomly interleaved sham trials where no stimulation is applied. Accuracy will be quantified in percentage correct. 1 Hour
Primary Working Memory Task Performance - Reaction Time In this task, a sequence of items (alphabets or numerals) is presented followed by a delay. Following this, a single item which may or may not have been in the sequence is presented and the subject will be asked to indicate whether the item was in the previously presented sequence. A total of 150 trials will be performed with randomly interleaved sham trials where no stimulation is applied. Reaction times will be quantified in milliseconds. 1 Hour
Secondary Intracranial EEG Spectral analysis and functional connectivity analysis of electrophysiology data will be performed using methods like multi-taper fft, wavelets, phase locking, Granger causality etc. The measures will be compared between sham and stimulation trials to identify if stimulation enhances neuronal entrainment. The correlation between the measures described above and the task performance will also be estimated. Intracranial EEG will be collected simultaneously when the participants perform the task. 1 Hour
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