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CompletedNCT04873804Updated May 5, 2021

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

An interventional study of Transcranial Direct Current Stimulation in Cognitive Symptom and Healthy, sponsored by Medipol University. Completed at 2 sites in Turkey. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-05-05.

Sponsored by Medipol University · Not applicable, Interventional, and Diagnostic

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Oct 2019, registered Apr 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
57
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Cognitive Symptom
  • Healthy

Keywords

  • tDCS
  • Dorsolateral Prefrontal Cortex
  • Posterior Parietal Cortex
  • Cognitive Function
03

In context

Neurobehavioral Manifestations

111 studies on the registry are indexed under Neurobehavioral Manifestations; 28 are open to participants now.

This study's enrollment of 57 is below the median of 71 across 84 interventional studies indexed under Neurobehavioral Manifestations.

Browse Neurobehavioral Manifestations studies →

Lead sponsor

Medipol University is the lead sponsor of 311 studies on the registry; 86 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • being 18-30 years old

Exclusion criteria

Exclusion Criteria:

  • alcohol and substance addiction
  • previous mental illness
  • having mental and cognitive problems
  • a history of head trauma
  • having cardiovascular disease.
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
57 participants (actual)

Study arms

  • Active comparator
    LEFT DLPFC

    The anode electrode of tDCS was applied to the left DLPFC and the cathode electrode was connected to the contralateral shoulder.

    Other: Transcranial Direct Current Stimulation

  • Active comparator
    RİGHT PPC

    The anode electrode of tDCS was applied to the right PPC and the cathode electrode was connected to the contralateral shoulder.

    Other: Transcranial Direct Current Stimulation

  • Sham comparator
    Sham

    Placebo was applied by placing the electrodes in the right PPC and left DLPFC without applying current.

    Other: Transcranial Direct Current Stimulation

Interventions

  • OtherTranscranial Direct Current Stimulation

    The intervention protocols were applied using tDCS (Teknofil TESsaNova). All individuals received 2 mA of anodal tDCS for 2 weeks on weekdays. All applications were done in the form of 20-minute sessions.

06

What researchers measure

Primary outcomes

  1. Neuropsychiatric Test Battery

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

    Time frame: 3 weeks

  2. Beck Depression Scale

    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

    Time frame: 3 weeks

07

Study locations

2 sites
  • Damla Ören
    Istanbul, 34000, Turkey
  • Medipol Mega Hospital
    Istanbul, 34000, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 5, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04873804
Lead sponsor
Medipol University
Responsible party
Damla Ören (Physiotherapist MSc, Medipol University) — Principal investigator
First posted
May 5, 2021
Start date
Oct 10, 2019
Primary completion
May 10, 2020
Completion
Jun 10, 2020
Last update
May 5, 2021

Study contacts

Miray Budak, PhD
principal investigator · Medipol University
Lutfu Hanoglu, PhD
study chair · Medipol University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2021. You cannot join it, but the record below documents what was studied.

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