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RecruitingNCT07682207

Accelerated iTBS feasibility for adults with PTSD and major depression

About this titleRead the official source — NCT07682207
Device studyAges 18+Canada
The study in practice

Understand this study

Who could participate?

Listed age limits: from 18 years.

What will I do during this study?

Participants complete health screening and baseline assessments, then receive six short iTBS sessions each day for five consecutive days (30 sessions total). Brain activity is measured with EEG (recording of the brain’s electrical activity). Follow-up assessments take place at weeks 2, 5 and 12.

Listed locations
LondonSee all locations and recruitment
Participation duration
5 treatment days, with follow-up through week 12
Number of visits
30 stimulation sessions

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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 dateEstimated: September 2026
Recruitment status
Recruiting
Enrollment listed in the registry
16
Sponsor
Lawson Research Institute of St. Joseph's
Sponsor type
Research institute
Study type
Device
Intervention type
Device
Locations
Canada
Age range
Over 18 Years
Official registry ID
NCT07682207
Official title
Show the full official title

Accelerated Intermittent Theta Burst Stimulation for Depression in Post-Traumatic Stress Disorder: A Single-Arm, Open-Label Feasibility Study

Recruitment & locations

Currently recruiting

London

Interested in joining this study?

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Lawson Research Institute of St. Joseph's, a research institute.

Who can participate?

Listed age limits: from 18 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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