Actively Recruiting

Phase Not Applicable
Age: 6Years - 12Years
All Genders
NCT06010966

Effect of iTBS on Children With ADHD

Led by First Affiliated Hospital of Zhejiang University · Updated on 2023-12-13

54

Participants Needed

1

Research Sites

152 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Attention Deficit/Hyperactivity Disorder (ADHD) is a common neurodevelopmental disorder characterized by persistent symptoms of attention deficit and/or hyperactivity/impulsivity . Currently, the first line drugs for treating ADHD are central stimulants such as Tomoxetine and Guanfaxine. However, there is a risk of drug abuse and misuse, which often affects sleep and appetite, only 50% of patients can fully tolerate. This project uses the iTBS stimulation on weekends, children with ADHD finish scale evaluation, magnetic resonance imaging analysis, and cognitive function before and after stimulation, This study explores its therapeutic effect on attention deficit in children and adolescents with ADHD.

CONDITIONS

Official Title

Effect of iTBS on Children With ADHD

Who Can Participate

Age: 6Years - 12Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of ADHD according to DSM-V
  • Age between 6 and 12 years old, any gender
  • Right-handed
  • Han nationality or born in Han nationality region
  • Disease duration longer than 6 months
  • Webster children's intelligence score of 70 or higher
  • Guardian agrees and signs informed consent form
Not Eligible

You will not qualify if you...

  • Presence of other mental disorders such as anxiety and depression
  • Widespread developmental disorders or other neurological developmental disorders
  • Serious diseases affecting important organs like heart and lungs
  • Epilepsy or tic disorder
  • Inability to tolerate or cooperate with rTMS treatment
  • Use of psychoactive drugs, antipsychotics, antidepressants, or mood stabilizers within 3 months before enrollment or during treatment, except minimum effective dose of Tomoxetine (1.2-1.4 mg/kg/day)
  • Webster's intelligence score below 70
  • Implantation of metal or electronic devices in the body (excluding the oral cavity), such as pacemakers

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

Department of Psychiatry, First Affiliated Hospital of Zhejiang University

Hangzhou, Zhejiang, China, 310000

Actively Recruiting

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Research Team

S

Shaohua Hu, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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