RECRUITING

A Neurosensory Account

Description

The goal of this study is to develop and test a novel pathophysiology of PTSD by integrating sensory cortical (SC) and amygdala-PFC dysfunctions into a tripartite Sensory-Prefrontal-Cortex-Amygdala (SPA) model.

Study Overview

Study Details

Study overview

The goal of this study is to develop and test a novel pathophysiology of PTSD by integrating sensory cortical (SC) and amygdala-PFC dysfunctions into a tripartite Sensory-Prefrontal-Cortex-Amygdala (SPA) model.

A Neurosensory Account of PTSD

A Neurosensory Account

Condition
Post Traumatic Stress Disorder
Intervention / Treatment

-

Contacts and Locations

Tallahassee

Leon County, Tallahassee, Florida, United States, 32306

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Right-handed
  • * With normal or corrected-to-normal vision and normal olfaction
  • * Between the ages of 18 and 50 years
  • * Meeting the tACS screening criteria (see List I below; e.g., lack of a serious head injury or loss of consciousness)
  • * Patients: Diagnosis of PTSD
  • * Patients: If taking psychotropic medications, medication stability in the past 2 months
  • * If having mild substance use disorder (for patients) or occasional substance use, abstention from use 48 hours before the experiment.
  • * A history of diagnosis for a major medical illness (e.g., cancer, metabolic syndrome, cardiovascular disease, inflammatory disorders) or a neurological disorder (e.g., seizure, stroke, Parkinson's disease).
  • * Patients: Concurrent Axis I diagnosis (depression, anxiety, and mild substance use disorder are allowed given their high comorbidity with PTSD).
  • * Healthy controls: A history of diagnosis for a DSM-5 Axis I disorder or current use of psychoactive medications.
  • * Severe psychiatric instability or severe situational life crises, including evidence of being actively suicidal or homicidal, or any behavior that poses an immediate danger to self or others.
  • * History of head trauma with unconsciousness (\> 5 minutes)
  • * Report that they regularly drink 3 or more alcoholic beverages a day.
  • * Report that they are unable to abstain from substance use (including alcohol, nicotine, cannabis, amphetamines, narcotics, solvents, cocaine, hallucinogens, tranquilizers, barbiturates, etc.) or sleep medication for 48 hours before being scanned.
  • * Are on calcium channel blockers (e.g., verapamil, nifedipine) or alpha-blockers (e.g., prazosin, terazosin) and are unable to stop these medications for a 48-hour period prior to scanning (to exclude the impact of these medications on the interpretation of fMRI/EEG).
  • * Failed Urine Drug Screening Test: A rapid urine screening test that utilizes monoclonal antibodies to detect elevated levels of specific drugs (including alcohol, amphetamines, benzodiazepines, barbiturates, cocaine, marijuana, opiates, etc.) in urine (iCup)
  • * Pregnancy based on urine test. The safety of MR systems has not been established for fetuses
  • * Having electrically, magnetically, or mechanically activated implants (e.g., cardiac pacemakers), because the electromagnetic fields produced by the MR system may interfere with the operation of these devices.

Ages Eligible for Study

18 Years to 50 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Florida State University,

Wen Li, PhD, PRINCIPAL_INVESTIGATOR, Florida State University

Study Record Dates

2027-10