common.study.topics.clinical

PTSD Questionnaire Test in Active Duty and Military Veterans

common.study.values.description

“An Evaluation of Two PTSD Assessments in an Active Duty and Military Veteran Sample”

Given the high prevalence of post-traumatic stress disorder (PTSD) in veterans and active duty military, the focus of this research study is to test the reliability of two new PTSD assessments, the Clinician Administered PTSD Scale for DSM-5 (CAPS-5) and the PTSD Symptom Scale Interview for DSM-5 (PSSI-5) and compare the results between the two new assessments and the previous "gold standard", the Clinician Administered PTSD Scale for DSM-IV (CAPS-IV). Biomarkers believed to be related to PTSD (e.g., biofluid biomarkers, cognitive and physiological markers, and neural activity as measured by EEG) will be collected to inform targeted interventions in specific groups of patients and other large-scale biomarker discovery efforts in the field. Participants will be 950 male and female active duty military and veterans ages 18 or older who have been exposed to at least one traumatic event.

common.study.values.location

participant.ui.study.affiliations-map.online-study.header-virtual

participant.ui.study.affiliations-map.online-study.text

participant.ui.study.affiliations-map.legend.locations participant.ui.study.affiliations-map.legend.selected

common.study.values.methods

No pharmaceutical medication involved common.study.methods.has-drugs-no
Patients and healthy individuals accepted common.study.methods.is-healthy-no

Diagnostic Test - CAPS-5

Clinician Administered PTSD Scale for DMS-5

Diagnostic Test - PSSI-5

PTSD Symptom Scale Interview for DSM-5

Diagnostic Test - CAPS-IV

Clinician Administered PTSD Scale for DSM-IV

participant.views.study.view.additional

participant.views.study.view.scientific-title

Psychometric Evaluation of the Clinician Administered PTSD Scale for DSM-5 (CAPS-5) and the PTSD Symptom Scale Interview for DSM-5 (PSSI-5) in an Active Duty and Military Veteran Sample

common.study.values.clinical-trial-id

NCT04180930

participant.views.study.view.id

dR6ELd