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Keep this study
Lead
Florida State University
The purpose of the present study is to examine the effects of transcranial magnetic stimulation (TMS) on cognitive control among individuals with posttraumatic stress disorder (PTSD).
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Over 18 years of age
Endorse lifetime exposure to at least one Criterion A traumatic event
Report clinically significant posttraumatic stress disorder (PTSD) symptoms (score of ≥ 33 on the PTSD Checklist for DSM-5 \[PCL-5\]).
You may not be if
Endorse medical contraindication for neuromodulation (e.g., ferrous metal in head, seizure disorder, brain tumor, stroke, aneurysm, multiple sclerosis, etc.)
Report an unstable medical condition or any current medical condition that precludes safe participation in the trial (e.g., unstable metabolic abnormality, unstable angina, etc.)
Report any history or diagnosis of dementia or other cognitive disorder, which may interfere with engagement
Report any history or diagnosis of Severe Traumatic Brain Injury
Report any history or diagnosis of Schizophrenia, Schizoaffective Disorder, Delusional Disorder or other psychotic illness, which precludes safe participation in the trial
Report a primary obsessive-compulsive disorder (OCD) diagnosis
Report an active substance use disorder (within last 3 months) or any current substance use that precludes safe participation in the trial
Report suicide risk that precludes safe participation in the trial, defined as clinical impression that the participant is at significant risk for suicide (i.e., greater than moderate level of suicide risk, in accordance with the Joiner et al. (1999) suicide risk framework)
Report an inability to stop taking any medication that significantly lowers the seizure threshold (e.g., tricyclic antidepressants, clozapine, etc.)
Report a current, planned, or suspected pregnancy
Clareo Health | Testing a Causal Model of Cognitive Control Deficits in Posttraumatic Stress Disorder (PTSD)
