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Functional Magnetic Resonance Imaging–Guided Personalization of Transcranial Magnetic Stimulation Treatment for Attention Deficit/Hyperactivity Disorder

Functional Magnetic Resonance Imaging–Guided Personalization of Transcranial Magnetic Stimulation Treatment for Attention Deficit/Hyperactivity Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109943
Enrollment
Unknown
Registered
2025-09-28
Start date
2025-09-30
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit/Hyperactivity Disorder

Interventions

Precision Positioning-rTMS intervention Group:Calculate the functional connectivity between the PCC effector brain regions and IPL, and select the position with the largest functional connectivity as
Non-precise positioning-rTMS intervention group:The random coordinates of voxels located more than 10mm away from the precise positioning coordinates within the IPL mask are used as the stimulation ta
Standard drug treatment group:This group only take methylphenidate for treatment as a reference for rTMS therapeutic effect.
Baseline group :NA

Sponsors

The Affiliated Hospital of Hangzhou Normal University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 16 Years

Inclusion criteria

Inclusion criteria: 1. Age: 8 to 16 years old; 2. Meet the diagnostic criteria for attention deficit hyperactivity disorder (ADHD) in the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) of the American Psychiatric Association; 3. No history of other mental disorders that affect cognitive function (such as intellectual disability) or organic brain diseases; 4. The IQ measured by the Wechsler Intelligence Scale for Children (WISC) is =80; 5. Obtain the written informed consent of the patient and their guardian.

Exclusion criteria

Exclusion criteria: 1. All contraindications for metal implants within the skull (such as cochlear implants, deep brain electrodes, etc.), pacemakers, intracardiac leads, etc., as well as all contraindications of magnetic resonance imaging scans, such as claustrophobia, etc. 2. Previous history of epilepsy: history of epileptic seizures, history of febrile convulsions in childhood; And those with epileptiform discharges shown on electroencephalogram; 3. Known brain injuries (such as tumors, stroke foci, etc.) or severe head trauma; 4. There has been a history of alcohol, drug or psychoactive substance abuse within the past six months; 5. Currently undergoing electroconvulsive therapy (ECT) or other nerve stimulation therapies (such as transcranial direct current stimulation (tDCS)); Those who have taken other psychotropic drugs within four weeks (except for methyl ester).

Design outcomes

Primary

MeasureTime frame
ADHD symptoms scores ;inhibition control;sustained attention;

Secondary

MeasureTime frame
Behavioral problems and social adaptation levels ;social interaction;Adaptive Behavior Assessment ;Functional Impairment Rating;Executive Function ;attention assessment;working memory;cognitive flexibility;Brain function and neural networks;

Countries

China

Contacts

Public ContactYufeng Zang

Hangzhou Normal University/ The Affiliated Hospital of Hangzhou Normal University

zangyf@hznu.edu.cn+86 186 0651 7380

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026