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Effect of rTMS on working memory

Phase 2
Conditions
working memory.
Person encountering health services in unspecified circumstances
Registration Number
IRCT201305131958N4
Lead Sponsor
Institute for Cognitive Science Studies
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Inclusion: voluntary and competent to consent; voluntary and competent to consent; between the ages of 18-65; considered a healthy individual free of psychopathology based on the General Health Questionnaire (GHQ28);
right-handed determined modified version of the Edinburgh Handedness Inventory; self-reported non-smoker;
Exclusion: Any kind of metal implement in head and body; Have a history of substance abuse; Have a medical or neurological illness; Have a history of seizures; Have a first degree relative with a history of a seizure disorder; pregnancy in female subjects.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Working memory capacity. Timepoint: Before and after intervention. Method of measurement: CANTAB cognitive tasks (Delay match to sample, spatial span, pattern recognition, stockings of cambridge) 2 back, digit span.
Secondary Outcome Measures
NameTimeMethod
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