Participate in a Research Study Exploring Non-Invasive Neuromodulation for PTSD

RESEARCH STUDY:

We are conducting a research study to better understand the safety and effectiveness of non-invasive vagus nerve stimulation (nVNS) for symptoms associated with post-traumatic stress disorder (PTSD). Participation in this study will not replace your usual clinical care, and no clinical treatment decisions will be made based solely on the research data collected.

Complete the screening form

ABOUT THE STUDY

This is an open-label research study, meaning all participants will receive treatment with the study device in addition to their ongoing care. The study includes an initial observation period followed by a 12-week at-home treatment period using the nVNS device applied to the neck. The device delivers brief electrical stimulation to the vagus nerve through the skin and does not involve surgery, implants, magnets, or radiation.

Adults diagnosed with PTSD who meet eligibility criteria may be invited to participate. Study participation involves regular symptom questionnaires, clinical assessments, and follow-up visits to help researchers evaluate the safety, tolerability, and potential impact of nVNS on PTSD symptoms over time.

WHO MAY PARTICIPATE

This study may be an option for:

Adults aged 18-70 years with a diagnosis of PTSD who meet all study eligibility requirements

WHAT DOES PARTICIPATION INVOLVE?

Up to 6 study visits over 16 weeks
Each study visit may last approximately 30 to 120 minutes
Study activities include completing surveys, clinician-administered assessments, and at-home use of an investigational device for PTSD symptoms
(The study includes an initial observation period before the treatment begins)