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The preliminary study of a single session of repetitive transcranial magnetic stimulation for the attentional impairments in developmental disorder

The preliminary study of a single session of repetitive transcranial magnetic stimulation for the attentional impairments in developmental disorder - The preliminary study of a single session of repetitive transcranial magnetic stimulation for the attentional impairments in developmental disorder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027000
Enrollment
60
Registered
2017-05-02
Start date
2017-05-02
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Individuals with ASD, individuals with ADHD, healthy subjects

Interventions

rTMS on rTPJ (facilitation, inhibition) rTMS on rTPJ (facilitation, inhibition) rTMS on rTPJ (facilitation, inhibition, sham)

Sponsors

Showa University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ASD group 1) Subjects who had received a clinical diagnosis of ASD in outpatient units of the Showa University Karasuyama Hospital. 2) Aged 20-49 years-old, male and female 3) No serious comorbid psychiatric disorders or medical illness. 4) Capability of informed consent ADHD group 1) Subjects who had received a clinical diagnosis of ADHD in outpatient units of the Showa University Karasuyama Hospital. 2) Aged 20-49 years-old, male and female 3) No serious comorbid psychiatric disorders or medical illness. 4) Capability of informed consent Healthy group 1) Aged 20-49 years-old, male and female 2) No serious psychiatric disorders or medical illness. 3) Capability of informed consent

Exclusion criteria

Exclusion criteria: 1) Subjects who are contraindicated for the use of MRI and TMS (e.g., implanted cardiac pacemaker, surgical aneurysm clips) 2) History of epilepsy, pregnancy, treatment with medication that can lower the seizure threshold. 3) Subjects who are judged as unsuitable for participation in this study

Design outcomes

Primary

MeasureTime frame
Cognitrax

Secondary

MeasureTime frame
Psychological tests including CANTAB

Countries

Japan

Contacts

Public ContactJunya Fujino

Showa University Medical Institute of Developmental Disabilities Research

fujinoj@med.showa-u.ac.jp03-5315-9357

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026