To evaluate the efficacy and safety of Software as a Medical Device in patients with Post-Traumatic Stress Disorder (PTSD)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
52
The subject will undergo treatment using the Software as a Medical Device
Clinician-Administered PTSD Scale for DSM-5
The primary objective of this study is to assess the change from baseline of the Clinician Administered PTSD Scale (CAPS - 5) score. Scores range from 0 - 80, with higher scores indicating increased PTSD symptom severity.
Time frame: baseline and after intervention (up to 21 weeks)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Yamanashi Prefectural Kita Hospital
Yamanashi, Hokkaido, Japan
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