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NCT05578209Active, not recruiting

Therapeutic Impacts of Theta Burst Stimulation Over Bilateral Posterior Superior Temporal Sulcus in Autism Spectrum Disorder

Therapeutic Impacts of Theta Burst Stimulation Over Bilateral Posterior Superior Temporal Sulcus in Autism Spectrum Disorder: a Comprehensive Study Integrating Clinical Symptoms, Neuropsychological Function and MRI

Source: ClinicalTrials.gov · Last updated 4 Jun 2025

Brief summary (registry, in English)

The investigator would like to investigate the impact of intermittent theta burst stimulation over bilateral posterior superior temporal sulcus in autism spectrum disorder

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
11 Oct 2022
Start date
3 Feb 2023
Primary completion date
Dec 2025
Lead sponsor
Chang Gung Memorial Hospital
Diseases
Autism
NCT number
NCT05578209

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 3 Feb 2023 to the primary completion date, Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous or current severe neurological disorder such as epilepsy, visual or hearing impairment
  • Previous or current severe systemic disease such as cardiovascular disease, diabetes or infection
  • Previous or current severe brain injury
  • Implementation of metal materials such as pacemaker or medication pump
  • Previous or current severe psychiatric disorders such as schizophrenia, bipolar disorder or substance abuse
  • Previous febrile seizures
  • Concurrent use of medications which increased the risk of seizure attack.

Other illness

  • History of brain surgery or nervous system infection, such as meningitis and encephalitis

Other

  • Pregnancy
  • Individuals with a significant brain abnormality such as intracranial space occupied lesions
  • Participate another clinical trial within one month.
  • Unable to complete MRI scan (claustrophobia)
  • Skin trauma on application site
  • Individuals with a large ischemic scar
  • Individuals suffering from multiple sclerosis
  • Individuals suffering from sleep deprivation during rTMS procedures
  • Individuals with a heavy consumption of alcohol
  • Individuals with a migraine headache from increased intracranial pressure

Who the study is looking for

  • Autism spectrum disorder, confirmed by Autism Diagnostic Observation Schedule II (CSS≧6)
  • No change in psychiatric drugs within one month

Age in the registry: 8 years to 30 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chang Gung Memorial Hospital
Coordinator of this site? Confirm its status
TaoyuanTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.