Non-invasive Neurostimulation as a Tool for Diagnostics and Management for Neurodegenerative Diseases

NCT ID
NCT05326750
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Kuopio University Hospital
Conditions
Alzheimer Disease, Dementia With Lewy Bodies, Frontotemporal Dementia

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 200 participants (Estimated).

What is being studied

  • Device: Gamma tACS (40 Hz) over the superior parietal cortex

Who may be eligible

Ages
18 Years to no maximum
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Mild Cognitive Impairment due to Alzheimer's disease * Dementia with Lewy Bodies * Frontotemporal dementia * Idiopathic normal pressure hydrocephalus (iNPH) Exclusion Criteria: * History of seizures * Pregnancy * Metal implants in the head (except dental fillings) * Electronic implants (i.e. pace-maker, implanted medical pump) * Age \<18 years

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: Finland

Sample of listed locations

  • Kuopio University Hospital — Kuopio, Finland — Recruiting

Study details

Start date
November 21, 2022
Primary completion date
July 1, 2032
Completion date
July 1, 2032
First posted
April 14, 2022

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT05326750
Registry last updated
October 2, 2026
QualifiedStudies registry data refreshed
October 12, 2026
QualifiedStudies record fetched
October 12, 2026

View NCT05326750 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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