Transcranial Alternating Current Stimulation (tACS) for the Treatment of Anxiety in Veterans: An Open-Label Pilot Study
Eligible age
19–70 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
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About this study
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.
Sponsor: Birmingham VA Health Care System
You may qualify if…
- ✓ Veteran of the U.S. military
- ✓ English-speaking and provides signed informed consent and HIPAA
- ✓ Adults ≤70 years of age
- ✓ Past week's GAD-7 of ≥10 which represents at least moderate level of anxiety
- ✓ If applicable, antidepressants may be continued if taking the concomitant medication for ≥8 weeks and at stable doses for ≥4 weeks
- ✓ Participants of child-bearing potential must have negative pregnancy test at entry and must agree to adhere to a medically acceptable method of birth control
You may not qualify if…
- ✕ Lifetime bipolar type I, schizophrenia spectrum, or other psychotic disorders based on VA medical records
- ✕ Current sedative-hypnotic, stimulant, inhalant and/or opioid use disorder within the past 6 months based on VA medical records and clinical interview
- ✕ Diagnosis of moderate to severe alcohol and/or cannabis use disorder within past 6 months based on VA medical records and clinical interview
- ✕ History of severe traumatic brain injury (TBI), defined by Ohio State University TBI Identification Method
- ✕ Dementia or related progressive neurocognitive disorder as per the medical record
- ✕ Use of prohibited medications (see list above) in the prior 2 weeks
- ✕ Increased risk of suicide that necessitates inpatient treatment, suicidal ideation/behavior endorsed on 6-item Columbia Suicide Severity Rating Scale screening questionnaire (yes" to question 4 or 5; or yes to # 6 as current), and/or suicidal behavior within past 90 days.
- ✕ Treatment with electroconvulsive therapy, vagus nerve stimulation, or transcranial magnetic stimulation within the past 6 months
Where it's recruiting
Birmingham
Source: ClinicalTrials.gov · NCT07288008 · last updated 2025-12-31