An open label home-administered transcranial Direct Current Stimulation (tDCS) clinical trial of Unipolar Depression

Brief description of study

The purpose of this research study is to determine the safety and efficacy of home-based noninvasive brain stimulation, transcranial direct current stimulation (tDCS), in treating unipolar depression. Patients who are candidates for FDA approved rTMS (repetitive Transcranial Magnetic Stimulation) and ECT (electroconvulsive therapy) may be eligible to participate in this home-based study.

Clinical Study Identifier: s20-01213 Identifier: NCT02894736
Principal Investigator: Leigh E. Charvet.
Other Investigator: Robert W Charlson.

If you are registered as a volunteer, please log in to contact the study team/express interest in this study.

Contact the research team to learn more about this study.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.