Clinical trial Recruiting at 1 site Interventional Ages 45 to 80

Effects of tDCS on cognition in mild cognitive impairment

Official title: The Effects of Specific Transcranial Direct Current Stimulation tDCS on Cognition in Mild Cognitive Impairment: A Novel Study Protocol

Run by Istanbul Medipol University Hospital · NCT05919485 · Data updated 2026-11-12

This study is testing whether a brain stimulation technique called tDCS can improve thinking skills in people with mild cognitive impairment related to Alzheimer's and Parkinson's diseases.

Quick facts

Study typeInterventional
Ages45 Years to 80 Years
SexAll
Enrollment120 (estimated)
SponsorIstanbul Medipol University Hospital
Academic / other
Locations1 site (Antalya, Alanya)
StatusRecruiting
StartedAugust 1, 2023
Main results expectedDecember 30, 2023
Study endsDecember 15, 2025
Registry record updatedMay 2, 2025
Trial IDNCT05919485 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are literate individuals aged 45-80 diagnosed with Parkinson's disease-MCI or amnestic MCI.

Probably not a fit

Patients with existing neurological or psychiatric disorders, signs of dementia, or those unable to undergo fMRI or tDCS may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effectiveness of transcranial direct current stimulation (tDCS) on cognitive skills in patients with mild cognitive impairment (MCI) related to Alzheimer's and Parkinson's diseases. The study involves a multicenter, randomized, controlled design where participants receive anodal tDCS applied to specific brain regions over 10 sessions within 14 days. Cognitive outcomes will be assessed using neurocognitive tests and brain connectivity will be analyzed through fMRI and EEG at various time points. The goal is to explore the potential cognitive benefits of tDCS and its implications for understanding MCI and Parkinson's disease.

Why it matters

Potential benefit: If successful, this study could lead to new non-invasive treatment options that help preserve cognitive function in patients with mild cognitive impairment.

How similar studies have gone: Other studies have shown promising results with tDCS in cognitive enhancement, indicating potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Providing an informed consent;
2. Literate and between 45-80 years of age;
3. 60 females and 60 males;
4. Diagnosed with PD based on criteria suggested by UK Parkinson's Disease Society, Brain Bank and PD-MCI in accordance with the diagnostic criteria suggestions by Litvan;
5. Diagnosed with aMCI based on diagnosis criteria (CDR\>0.5) suggested by Petersen;
6. On a stable pharmacological treatment minimum for one month with no washout period.

Exclusion Criteria:

* Illiterate or education level less than primary school
* Having an existing and/or prior neurological disease; psychiatric disease or head trauma; and/or irreversible hearing or sight problems or other medical illness (e.g. diabetes mellitus, hypertension);
* Exhibiting signs of dementia for PD group ;
* Having medical issues that prevent undergoing fMRI or for tDCS application.

Where it's running

  • Alanya Alaaddin Keykubat Üniversitesi
    Antalya, Alanya, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.