MedPath

Dual Site-Dual Channel Non-invasive Brain Stimulation for Language and Cognitive Function in Healthy Subjects

Not Applicable
Completed
Conditions
Healthy
Interventions
Device: IFG stimulation
Device: DLPFC stimulation
Device: Sham stimulation
Registration Number
NCT03486808
Lead Sponsor
Samsung Medical Center
Brief Summary

The aim of this study is to investigate the effect of dual site-dual channel non-invasive brain stimulation for recovery of language and cognitive function in healthy. Simultaneous dual site-dual channel stimulation was applied by using two sets of transcranial direct current stimulation devices. All subjects will go through four conditions of transcranial direct current stimulation with for 30 minutes. Four conditions are 1) Dual stimulation: i) anodal stimulation on left inferior frontal cortex, ii) anodal stimulation on left dorsolateral prefrontal cortex. 2) IFG stimulation: anodal stimulation on left inferior frontal cortex; 3) DLPFC stimulation: anodal stimulation on left dorsolateral prefrontal cortex area. 4) sham stimulation

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
27
Inclusion Criteria
  • healthy subjects with age over 19 years old
Read More
Exclusion Criteria
  • history of disorders involving central nervous system
  • patients with severe medical or psychiatric disease
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Dual stimulationIFG stimulationi) anodal stimulation of left inferior frontal cortex ii) anodal stimulation on left dorsolateral prefrontal cortex
DLPFC stimulationDLPFC stimulationanodal stimulation on left dorsolateral prefrontal cortex
Sham stimulationSham stimulationsham stimulation
Dual stimulationDLPFC stimulationi) anodal stimulation of left inferior frontal cortex ii) anodal stimulation on left dorsolateral prefrontal cortex
IFG stimulationIFG stimulationanodal stimulation of left inferior frontal cortex
Primary Outcome Measures
NameTimeMethod
Verbal 3 back testBaseline and after intervention (approximately 30 minutes)

measure working memory

Korean Boston naming testBaseline and after intervention (approximately 30 minutes)

measures naming ability thorough picture naming test

Secondary Outcome Measures
NameTimeMethod
Korean Color Word Stroop testBaseline and after intervention (approximately 30 minutes)

measures selective attention and executive function

Controlled Oral Word Association TestBaseline and after intervention (approximately 30 minutes)

measure verbal fluency

Trial Locations

Locations (1)

Samsung Medical Center

🇰🇷

Seoul, Korea, Republic of

© Copyright 2025. All Rights Reserved by MedPath