Actively Recruiting

Phase 1
Phase 2
Age: 10Years - 18Years
All Genders
NCT07084649

Dual-target iTBS for Youth With ADHD

Led by Shanghai Mental Health Center · Updated on 2025-07-24

15

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will employ accelerated intermittent theta burst stimulation (aiTBS) targeting two transcranial magnetic stimulation (TMS) sites: the right inferior frontal gyrus and left inferior parietal lobule.

CONDITIONS

Official Title

Dual-target iTBS for Youth With ADHD

Who Can Participate

Age: 10Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with ADHD according to DSM-5 criteria
  • Ages 10 to 18 years, any gender
  • Full-scale IQ above 70 on the China-Wechsler Intelligence Scale for Children
  • Score above 1 on SNAP-IV Parent Rating Scale (inattention/hyperactivity-impulsivity) and above 2 on Clinical Global Impression-Severity Scale after medication
  • Score of 1.6 or higher on Inattention or Hyperactivity/Impulsivity subscale of SNAP-IV
  • Either medication-nafve, off medication, or on stable medication for at least 4 weeks before baseline and throughout the study
  • No use of psychostimulant medications
  • Right-handed
Not Eligible

You will not qualify if you...

  • Contraindications for TMS therapy such as epilepsy, cardiac pacemakers, cochlear implants, or metal implants
  • Contraindications for MRI including metal implants in the body, claustrophobia, or tattoos
  • History of epilepsy, organic brain disorders, traumatic brain injury, or severe physical illnesses
  • History of violent or suicidal behavior
  • Comorbid neurodevelopmental disorders like autism spectrum disorder or tic disorders
  • Other primary psychiatric disorders except conduct disorder/oppositional defiant disorder, mild anxiety, or depression
  • Substance abuse
  • Receiving any non-medical treatments such as cognitive behavioral therapy or neurofeedback
  • Female participants who are pregnant or breastfeeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai Mental Health Center

Shanghai, None Selected, China, 200030

Actively Recruiting

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Research Team

H

Huiru Cui, Ph.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

3

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