Fisher Wallace Neurostimulation & Depression Study
Running, not enrolling · Not applicable · Has a placebo group
Conditions studied: Major Depressive Disorder
In brief
Examine the safety and effectiveness of the Fisher Wallace Cranial Electrotherapy Stimulator Device on Major Depressive Disorder using two 20-minute per day treatment sessions over eight weeks.
Key facts
- Study ID
- NCT04541563
- Run by
- ProofPilot
- People needed
- 175
- Starts
- 2020-08-24
- Expected to finish
- 2021-11-30
- Last updated by the study team
- 2021-02-11
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age greater than or equal to 21
- US resident
- Can receive packages to their home via UPS/Fedex/USPS
- Major Depressive Disorder
- PHQ-8 Score greater than 10 (show some signs of mild to moderate depression)
- PHQ-8 Score less than 20 (given remote study serious depressed should be excluded)
- Read/write English
- have not contemplated suicide in the past year
- not been institutionalized for mental health issues.
- not currently experiencing problems with alcohol or drug abuse
- can commit to not drinking alcohol 4 hours before bedtime for the duration of the study
- can commit to two (2) 20 minute sessions per day for 8 weeks
- has not used a brain stimulation treatment in one year
- no suspected or known history of heart disease
- no pacemaker
- not under medical supervision for other serious medical condition
- not taking opioids
- is a resident of states in which we have licensed medical professionals
Where it is running
- ProofPilot (Remote Virtual Trial) — New York, New York, United States
Full record on ClinicalTrials.gov
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