Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
All Genders
Healthy Volunteers
ID06464445

Defining Parameters to Optimize Neurostimulation for the Treatment of Pediatric Depression

Led by Université de Sherbrooke · Updated on 2025-02-10

30

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research investigates different parameters of intermittent theta burst transcranial magnetic stimulation (iTBS), a type of repetitive TMS used to alter brain activity and promote brain plasticity. The study focuses on how the shape and duration of electromagnetic pulses during iTBS affect the brain's ability to reorganize itself, aiming to improve treatment methods for depression that does not respond to usual therapies. Participants will receive three different iTBS protocols, each separated by a week. The protocols involve different pulse shapes and durations: monophasic pulses, biphasic pulses, and long monophasic pulses. Each protocol uses pulses delivered at 80% of the resting motor threshold, with specific frequency and timing settings. The sequence of these protocols will be randomized for each participant. During the study, brain activity will be monitored before and after each iTBS session to measure cortical plasticity, with assessments every five minutes up to one hour post-intervention. Participants will be involved in multiple sessions with these measurements to understand the effects of each protocol. The study will also monitor participant health and any reactions throughout the process, with the total participation duration spanning several weeks due to the multiple study visits and washout periods.

CONDITIONS

Brief Title

Optimization of ITBS for Depression

Who Can Participate

Age: 18Years - 35Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 18 and 35 years old
  • Be right-handed
  • Be in good health
Not Eligible

You will not qualify if you...

  • Have an implant or pacemaker
  • Have tinnitus
  • Have a history of fainting
  • Have had an epileptic seizure or have a family history of epilepsy
  • Have a known neurological disease
  • Be under psychotropic medication
  • Have suffered from substance abuse or dependence in the last 6 months
  • Have a neurostimulator
  • Have a splinter or metallic implant in the head or body
  • Have a cochlear implant
  • Have an automated injection system implanted (insulin pump)
  • Have a transdermal patch
  • Have tattoos in the area to be studied
  • Be pregnant or breastfeeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - 3 weeks

Participants receive three different intermittent theta burst stimulation (iTBS) device protocols, each separated by one week. The order of the iTBS protocols will be randomized.

3 visits (in-person), one per week for each iTBS protocol

Trial Site Locations

Total: 1 location

1

Centre de recherche du Centre hospitalier universitaire de Sherbrook

Sherbrooke, Quebec, Canada, J1H 5H3

Actively Recruiting

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Research Team

S

Samantha Cote, Ph.D.

J

Jean-Francois Lepage, Ph.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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