Study of brain activity changes by electrical stimulation on scalp and rehabilitatio

Phase 1

Recruiting

• Conditions: Central Nervous System Diseases; neurological disorders; D002493

• Registration Number: JPRN-jRCT1052220196
• Lead Sponsor: Koganemaru Satoko

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-03-17
• Last Update Posted: 17 October 2023

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 neuology or otorhinolaryngology, Kyoto University Hospital or Murata Hospital
2 Patients who have developed cerebrovascular disorders, neurodegenerative diseases, involuntary movement diseases, neuroinflammatory 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 Other patients who are deemed unsuitable for the safe conduct of this study, such as those who are unable to remain at rest.

Study & Design

• Study Type: Interventional
• Study Design: Not specified