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The Effect of Transcranial Direct Stimulation on Cognitive Functions of Healthy Adults

Not Applicable
Completed
Conditions
Healthy
Cognitive Symptom
Registration Number
NCT04873804
Lead Sponsor
Medipol University
Brief Summary

Background: Transcranial direct current stimulation(tDCS) has been used to improve cognitive functions in healthy young adults.

Purpose: To investigate the effect of TDCS application on different cortex regions on cognitive function.

Methods: Sixty individuals aged 18-30 were included in the study. The participants were randomly divided into the left dorsolateral prefrontal cortex (Left DLPFC Group)(n=20), the right posterior parietal cortex (Right PPC Group)(n=20), and the sham group (Sham Group)(n=20). tDCS was applied for 20 minutes on weekdays for 2 weeks. The participants were evaluated in terms of cognitive functions with Neuropsychometric Test Battery before and after treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
57
Inclusion Criteria
  • being 18-30 years old
Exclusion Criteria
  • alcohol and substance addiction
  • previous mental illness
  • having mental and cognitive problems
  • a history of head trauma
  • having cardiovascular disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Neuropsychiatric Test Battery3 weeks

It is a test battery for getting detailed information about general cognitive status.

Beck Depression Scale3 weeks

It measures the symptoms seen in depression such as emotional, cognitive and motivational. It includes 21 items determine a behavioral feature related to depression. Items are numbered from 0 to 3. The goal is to objectively break down the degree of symptoms.

The total score of all answers is calculated as follows:

0 to 9 points: Minimally depressive symptoms 10 to 16 points: Mild depressive symptoms Between 17 and 29 points: Moderate depressive symptoms Between 30 and 63 points: Severe depressive symptoms

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Damla Ören

🇹🇷

Istanbul, Turkey

Medipol Mega Hospital

🇹🇷

Istanbul, Turkey

Damla Ören
🇹🇷Istanbul, Turkey

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