Multimodal Image Analysis and Guidance of Neuromodulation for Trauma-Related Symptoms

Description

MAGNETS is a prospective, randomized, parallel-design, sham-controlled clinical trial of accelerated, functional magnetic resonance imaging (fMRI)-guided intermittent theta burst stimulation (iTBS) to the right dorsolateral prefrontal cortex (dlPFC) for chronic symptoms of posttraumatic stress disorder (PTSD) in a comorbid Veteran population.

Conditions

Posttraumatic Stress Disorder

Study Overview

Study Details

Study overview

MAGNETS is a prospective, randomized, parallel-design, sham-controlled clinical trial of accelerated, functional magnetic resonance imaging (fMRI)-guided intermittent theta burst stimulation (iTBS) to the right dorsolateral prefrontal cortex (dlPFC) for chronic symptoms of posttraumatic stress disorder (PTSD) in a comorbid Veteran population.

Multimodal Image Analysis and Guidance of Neuromodulation for Trauma-Related Symptoms

Multimodal Image Analysis and Guidance of Neuromodulation for Trauma-Related Symptoms

Condition
Posttraumatic Stress Disorder
Intervention / Treatment

-

Contacts and Locations

Albuquerque

UNM Center for Psychiatric Research, Albuquerque, New Mexico, United States, 87106

Albuquerque

New Mexico VA Health Care System, Albuquerque, New Mexico, United States, 87108

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

  • * Veterans will be enrolled in this study if they:
  • 1. are aged 18-80;
  • 2. have a documented diagnosis of PTSD with evidence of ongoing symptoms as demonstrated by score of "31" or higher on the PCL-5, a measure of posttraumatic stress symptoms;
  • 3. are fluent in English (as the neuropsychological testing tools used are only available in English) and
  • 4. have been on stable doses of psychotropic medications for the past month.
  • * Veterans will be excluded from participation in this study if there is:
  • 1. a prior history of other neurological disease beyond mild TBI, as determined by VA/DoD criteria for TBI severity;
  • 2. any history of seizures beyond immediate posttraumatic seizure or childhood febrile seizure, so as to reduce risk of exacerbation of epilepsy or other neurological symptoms;
  • 3. history of a psychotic disorder, such as schizophrenia or bipolar disorder, so as to reduce risk of psychiatric decompensation;
  • 4. active substance/alcohol dependence without ongoing treatment, to reduce confounding effects on diagnosis and brain imaging;
  • 5. presence of any implanted electrical device (e.g., pacemaker), to reduce risk of device malfunction from rTMS;
  • 6. recent medical hospitalization (within four weeks), to reduce risk of medical decompensation during the study;
  • 7. any condition that would prevent the subject from completing the protocol;
  • 8. appointment of a legal representative or inability to provide informed consent, to avoid coercion of a vulnerable population;
  • 9. any ongoing litigation related to PTSD, TBI, disability determination, or service connection, to prevent interference with legal proceedings;
  • 10. any contraindication to MRI;
  • 11. pregnant women, so as to prevent complications;
  • 12. membership in an identified vulnerable population, including minors and prisoners, so as to prevent coercion;
  • 13. Cognitively impaired adults who lack capacity to consent.

Ages Eligible for Study

18 Years to 80 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of New Mexico,

Study Record Dates

2027-10-01