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Modulation of Visual-Spatial Learning in Patients With Mild Cognitive Impairment (MCI) by tDCS

Modulation of Visual-Spatial Learning in Patients With Mild Cognitive Impairment (MCI) by Transcranial Direct Current Stimulation - Proof of Principle and Mechanisms

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02110043
Enrollment
21
Registered
2014-04-10
Start date
2014-03-31
Completion date
2017-10-31
Last updated
2021-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Impairment (MCI)

Keywords

mild cognitive impairment (MCI), tDCS, LOCATO task, visual-spatial learning

Brief summary

The aim of this study is to investigate whether a combination of intensive training of visual-spatial abilities (LOCATO task) with anodal transcranial direct current stimulation (tDCS) leads to an improvement in learning and memory in patients with mild cognitive impairment (MCI) and to examine the underlying neuronal mechanism.

Interventions

DEVICEtDCS

transcranial direct current stimulation (tDCS)

BEHAVIORALtraining

intensive training of visual-spatial abilities (in LOCATO task)

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

(MCI patients): * right handedness * amnestic and amnestic plus MCI with: 1. subjective memory impairment; 2. objective memory difficulties, at least 1 SD below gender, age and education adjusted standard values; 3. relatively normal performance in other cognitive domains; 4. no constraints in activities of daily livings 5. age: 50-90 years

Exclusion criteria

* severe internal or psychiatric disease * epilepsy * other severe neurological diseases, e.g. previous major stroke or brain tumor * DMS-IV manifest dementia * contraindication for MRT (claustrophobia, metallic implants, tattoos)

Design outcomes

Primary

MeasureTime frameDescription
Performance in LOCATO task (Visual-spatial learning and memory) after a combination of intensive visual-spatial training and tDCSimmediately after end of a 3-day period of training in tDCS condition vs sham conditionInvestigation whether the combination of intensive visual-spatial training (LOCATO task) and tDCS leads to improvement of visual-spatial learning and memory measured by performance in LOCATO task after end of a 3 day period of training compared to sham stimulation.

Secondary

MeasureTime frameDescription
functional changes: Connectivityend of 3-day cognitive training vs baselineConnectivity (measured by resting-state fMRT and correlation analysis) at baseline compared to end of 3 day period of training
cortical excitabilityat baselinecortical excitability measured by transcranial magnetic stimulation (TMS)
Quality of Lifeafter 1 month vs baselinequality of life as measured by standardized questionaire at baseline compared to quality of life measured 1 month after intervention (training and stimulation vs. training and sham-stimualtion)
long term effectsafter 1 month vs baselinelong term effects measured by performance in LOCATO task in tDCS condition after end of cognitve training and after 1 month compared to control conditions
affective stateimmediately after the end of 3-day cognitive training, after 1 month vs. baselineaffective state measured at baseline compared to affective state measured after the end of a 3-day cognitve training period and after 1 month (posttraining) in training and stimulation vs. training and sham stimulation
genotyping of learning related polymorphismsonceTo assess predictors of positive reaction to brain stimulation, genotyping of several learning related polymorphisms will be performed (i.e., APOE, BDNF Val66Met, COMT Val158Met).
memoryimmediately after end of 3-day of cognitive training, after 1 month vs. baselinememory performance tested at baseline compared to memory performance after the end of a 3-day cognitive training period and after 1 month (posttraining) in training and stimulation vs. training and sham stimulation

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026