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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01877161
Other study ID # E-1206-158-003
Secondary ID
Status Completed
Phase N/A
First received March 11, 2013
Last updated May 20, 2014
Start date December 2012
Est. completion date May 2013

Study information

Verified date May 2014
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Repetitive transcranial magnetic stimulation induced virtual lesions for aphasia.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- fluent in Korean

- older than 18 years old

Exclusion Criteria:

- younger than 18 years old

- psychotic or psychiatric problems

- pregnant

- contraindications to MRI/fMRI

- uncooperative

- metalic implants, pacemaker or cochlear implants

- cannot perform outcome measure-related task

- known seizure history

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Repetitive magnetic stimulation to superior temporal gyrus
Repetitive magnetic stimulation to superior temporal gyrus
Repetitive magnetic stimulation to middle temporal gyrus
Repetitive magnetic stimulation to middle temporal gyrus
Repetitive magnetic stimulation (Sham)
Repetitive magnetic stimulation (Sham)

Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam-si Bundang-gu

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Change of Reaction Time Between Before and After Stimulation in Each Session (MTG, STG, Sham) Reaction time for lexical and repetition test were measured before and after the TMS stimulation at each sessions (at session 1, session 2, session 3 over MTG/STG/Sham).
Response times were measured via the response pad, and spoken responses were recorded via a SV-1 Voice Key apparatus.
The "reaction time post TMS - reaction time pre TMS" were used for analysis.* Arm/Group Title Arm/Group Description Maximum length (999) Repetitive magnetic stimulation (rTMS) were applied over STG
change between before and after the TMS stimulation for each sessions (at session 1, session 2, session 3) No