Purpose

This proposal aims to study the role that the dorsal prefrontal cortex plays in human social cognition.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  1. 18 years old or older 2. patients able to give informed consent

Exclusion Criteria

  1. Children under 18 2. Significant co-morbidities 3. Claustrophobia or general anxiety that may impact intraoperative testing 4. Use of CNS-active medications including stimulants and antipsychotics which may alter 5. Pregnancy 6. Operative events that will require expedition of the surgery. 7. Poor tolerance of testing by the patient 8. Increased abnormal cortical excitability 9. Necessity to administer drugs that will interfere with mapping

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Intervention Model Description
Human subjects undergoing clinically planned neurosurgical procedures
Primary Purpose
Basic Science
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Neurosurgical subjects
Subjects undergoing intracranial neurosurgical procedures
  • Behavioral: Behavioral testing during neuronal recordings
    Participants undergoing clinically planned neurosurgical procedures will undergo single-neuronal recordings as they perform brief behavioral tasks.

Recruiting Locations

Massachusetts General Hospital
Boston, Massachusetts 02114
Contact:
Ziv Williams, MD
617-312-6534
zwilliams@mgh.harvard.edu

More Details

Status
Recruiting
Sponsor
Massachusetts General Hospital

Study Contact

Ziv Williams, MD
6173126534
zwilliams@mgh.harvard.edu

Detailed Description

Despite ongoing progress in the understanding of social behavior, little is known about the single-neuronal mechanisms that underlie human social cognition. The investigators will obtain single-neuronal recordings from the prefrontal cortex in participants undergoing clinically planned deep brain stimulation (DBS) electrode placement. The study population will consist of subjects undergoing planned DBS placement. Prospective participants will be selected for surgery irrespective of their participation in the study. After consenting to the study, the participants will be allowed to withdraw from participation at any time. No control subjects will be used. Instead, each subject will act as their own control based on task performance. For the study, neuronal recordings will be integrated within planned neurosurgical care and will be obtained from the prefrontal cortex as participants perform a brief behavioral task. During recordings and prior DBS placement, the participants are normally asked to make movements or answer questions based on verbal cues to aid in targeting the correct areas. The participants will be additionally asked to perform a brief linguistic-based task in which scenarios containing social agents are presented to the participants and in which they have to verbally describe/answer questions about them. Following cortical recordings and stimulation, the standard clinical procedure and DBS electrode placement proceeds as planned. The neuronal and behavioral data will then be analyzed off-line.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.