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RecruitingNCT06528938

Comparing accelerated and standard brain stimulation for adolescent depression

About this titleRead the official source — NCT06528938
Device studyAges 16–19Canada
The study in practice

Understand this study

Who could participate?

Listed age limits: 16 years to 19 years.

What will I do during this study?

Adolescents are assigned to one of two fMRI-guided iTBS schedules, both targeting the left prefrontal cortex. The accelerated group receives three sessions each weekday for two weeks; the standard group receives one session each weekday for six weeks.

Listed locations
OttawaSee all locations and recruitment

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What to know before participating

A point to clarify

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 dateStarted: August 1, 2024
Recruitment status
Recruiting
Enrollment listed in the registry
10
Sponsor
The Royal Ottawa Mental Health Centre
Sponsor type
Unknown or unclear
Study type
Device
Intervention type
DEVICE
Study phase
Not clearly listed
Locations
Canada
Age range
From 16 Years to 19 Years
Official registry ID
NCT06528938
Official title
Show the full official title

Randomized Pilot Trial Comparing the Feasibility and Efficacy of Accelerated vs. Standard fMRI-guided iTBS in Treatment-Resistant Depression in Adolescents

Recruitment & locations

Currently recruiting

Ottawa

Interested in joining this study?

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is The Royal Ottawa Mental Health Centre.

Who can participate?

Listed age limits: 16 years to 19 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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