Transcranial Alternating Current Stimulation (tACS) for the Treatment of Anxiety in Veterans: An Open-Label Pilot Study (NCT07288008)
๐ฉบ Plain-English Summary (8th-Grade Level)
Transcranial alternating current stimulation (tACS) in a wearable brain stimulation device that delivers a low intensity, pulsed, alternating current via scalp electrodes. Prior sham-controlled clinical trials have shown the therapeutic effects and safety of tACS for the treatment of anxiety and depression. In addition, tACS is rapid acting and well tolerated. After the device is issued to the patient during an in-office orientation and training session, the tACS device can be safely used by the patient at the convenience of their own home. Up to 40 Veterans under that age of 70 who have clinically significant anxiety will be enrolled in an 8-week open-label trial of Model FW-200 tACS to evaluate feasibility, acceptability, adherence and impact on anxiety, depression, post-traumatic stress disorder (PTSD), sleep and neurocognitive measures. Participants may have a concurrent diagnosis of major depressive disorder (MDD) and/or PTSD.
Who can join: Review the eligibility criteria below.
Location: Birmingham VA โ Birmingham, Alabama
Age range: 19 Years to 70 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Birmingham VA โ Birmingham, Alabama
๐ Contact the Study Coordinator
Phone: (205) 933-8101
Email: lori.davis@va.gov
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Anxiety
- Intervention Trial for Healthcare Workers With Anxiety โ Los Angeles, California
- Smartphones Aggravating Anxiety Symptoms โ Rochester, Minnesota
- Digital Single Session Intervention for Youth Mental Health โ Indianapolis, Indiana
- Testing FIRST in Youth Outpatient Psychotherapy โ Cambridge, Massachusetts
- Novel Mental Health Therapies to Improve Military Readiness โ Nellis Air Force Base, Nevada
- Brain Stimulation & Generalized Anxiety Study โ New York, New York
Explore by condition: All Anxiety clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.