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RecruitingNCT07657234

High-intensity tDCS safety and feasibility for late-life depression

About this titleRead the official source — NCT07657234
Device studyAges 60+United States
The study in practice

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Who could participate?

Listed age limits: from 60 years.

Listed locations
DallasSee all locations and recruitment
Study phase
Phase 1 / Phase 2This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.

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What to know before participating

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This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateEstimated: October 2026
Recruitment status
Recruiting
Enrollment listed in the registry
20
Sponsor
Andre Russowsky Brunoni
Sponsor type
Unknown or unclear
Study type
Device
Intervention type
Device
Study phase
Phase 1 / Phase 2This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
Locations
United States
Age range
Over 60 Years
Official registry ID
NCT07657234
Official title
Show the full official title

High-Dose Spaced Bilateral tDCS for Late-Life Depression: Open-Label Pilot Study

Recruitment & locations

Currently recruiting

Dallas

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Andre Russowsky Brunoni.

Who can participate?

Listed age limits: from 60 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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