Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:30 PM
Ignite Modification Date:
2025-12-24 @ 5:30 PM
NCT ID:
NCT03952468
Eligibility Criteria:
Inclusion Criteria:
-Suicide attempt or suicidal ideation with intent to make a suicide attempt within 48 hours of hospitalization as indicated on the hospital chart and confirmed by administration of the C-SSRS.
Exclusion Criteria:
* Primary psychotic disorder
* Bipolar disorder
* Cognitive impairment which would interfere with adequate participation in the project (MMSE \< 20).
* For safety, participants must meet established screening criteria safety during MRI, which is implemented as a conservative measure given the application of TMS in this population, since MRI involves magnetic fields at similar intensity to those emitted from the stimulation coil. These measures require a patient not having the following (unless MRI-safe):
* Cardiac pacemaker
* Implanted device (deep brain stimulation) or metal in the brain, cervical spinal cord, or upper thoracic spinal cord.
* TMS-specific exclusions are:
* pregnancy/lactation, or planning to become pregnant during the study
* lifetime history of moderate or severe traumatic brain injury (TBI)
* Current unstable medical conditions
* Current (or past if appropriate) significant neurological disorder
* Lifetime history seizure disorder
* Primary or secondary CNS tumors
* Stroke
* Cerebral aneurysm.
* Other exclusions are conditions that would like to be worsened by TMS, such as bipolar disorder
* Place Veterans at greater risk of seizures from TMS, such as severe and uncontrolled substance use disorder
* Inability to participate in CBT
* Other conditions or circumstance that, in the opinion of the investigator team, has the potential to prevent study completion and/or to have a confounding effect on outcome assessments
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT03952468
Study Brief:
Protocol Section:
NCT03952468