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Although research in this field has notably increased in recent years, it is still very scarce and the most effective stimulation parameters in terms of frequency, intensity, localization and length of stimulation, are unknown.

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An oral informed consent procedure is based on the same principle: you have to inform the data subject, followed by asking explicit consent.

To be consistent with pregnancy as a contraindication for volunteers in TMS studies, researchers who are pregnant should not deliver TMS.

Relapses do occur and may require periodic additional sessions.

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Research: TMS Therapeutics would like permission to use anonymous data regarding treatment parameters and responses to treatment as part of research efforts to better understand how to maximize the use of TMS.

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