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Brain activity changes induced by magnetic stimulation on scalp and rehabilitatio

Phase 1
Recruiting
Conditions
Central Nervous System Diseases
neurological disorders
D002493
Registration Number
JPRN-jRCT1052210202
Lead Sponsor
Koganemaru Satoko
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
160
Inclusion Criteria

1 Patients who are 18years of age or older at the time of consent to participate in the study and are undergoing medical treatment at the outpatient or inpatient department of Kyoto Ohara Memorial Hospital, Kyoto Konoe Rehabilitation Hospital, Gosyo Minami Rehabilitation Clinic, or Kyoto University Hospital neurology or otorhinolaryngology departments
2 Patients who have developed cerebrovascular disorders, neuromuscular degenerative diseases, involuntary movement diseases, neuromuscular inflammatory diseases , central neurological disorders, or traumatic central neurological disorders, and for whom the diagnosis has been established by neurological findings, imaging findings
3 6 days or more after the onset of symptoms, or 6 days or more after the recurrence of symptoms
4 Patients suffering from any of the following disorders due to neurological diseases: motor disorder, higher brain dysfunction, language disorder, and dysphagia.
5 Patients who have given a full explanation and have given written consen from the person or proxy if written consent from the person is difficult to obtain.

Exclusion Criteria

1 5 days or more before the onset of symptoms, or 5 days or more before the recurrence of symptoms
2 Patients who are difficult to communicate due to significant hearing impairment
3 Patients who have a cardiac pacemaker
4 Ptients who has metals in the body which cannot be confirmed to be non-magnetic
5 Those who are judged inappropriate as a participant by the Transcranial Magnetic Stimulation Test / Pre-Checklist and MR Test Pre-Checklist.
6 Those who are with claustrophobia
7 Any other person who is judged by the principal investigator to be inappropriate as a research subject

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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