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Supporting Episodic Memory With Transcranial Direct Current Stimulation in Healthy Controls and Dementia Patients

Supporting Episodic Memory With Transcranial Direct Current Stimulation in Healthy Young and Elderly Participants as Well as in Individuals With Memory Impairment

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03227185
Enrollment
55
Registered
2017-07-24
Start date
2017-10-01
Completion date
2019-10-19
Last updated
2020-02-28

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

Conditions

Alzheimer Disease, Healthy, Mild Cognitive Impairment

Brief summary

Previous studies showed that anodal tDCS applied over the dorsolateral prefrontal cortex (DLPFC) improved episodic memory performance, indicating a possible use as an intervention for patients suffering from memory impairments. At the same time, only scant evidence (provided by functional magnetic resonance imaging (fMRI) and magnetic resonance spectroscopy (MRS)) exists regarding the underlying mechanisms, thus hindering a more targeted application. The present study aims at establishing a connection between the stimulation-induced change in episodic memory performance on the behavioural level and neurophysiological parameters. TDCS effects and the underlying mechanisms will be compared between different study conditions, receiving either real anodal tDCS or sham stimulation over the left dorsolateral prefrontal cortex during an episodic memory task.

Interventions

DEVICEreal anodal transcranial direct current stimulation (tDCS)

The MR-compatible neuroConn DC-Stimulator MR (neuroCare Group, Ilmenau, Germany) will be used in the study.

DEVICEsham transcranial direct current stimulation (tDCS)

The MR-compatible neuroConn DC-Stimulator MR (neuroCare Group, Ilmenau, Germany) will be used in the study.

Sponsors

University of Bern
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Intervention model description

Participants will be randomly assigned to two possible sequences of stimulation conditions. Group 1 will receive real tDCS stimulation to the left dlPFC during encoding on the first day and sham stimulation on the second day, and group 2 will receive sham stimulation during encoding on the first day and real tDCS on the second day. The participants will be randomized with equal probability to each of the two groups, using block randomization..

Eligibility

Sex/Gender
ALL
Age
20 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Written informed consent * Right-handedness * Non-smokers * Native German speakers or comparable level of fluency * Normal or corrected-to-normal vision

Exclusion criteria

* Neurological or psychiatric condition (other than diagnosed cognitive impairment) * Past head injuries * Magnetizable implants * History of seizures * Current or life-time alcohol or drug abuse * Pregnancy * Skin diseases

Design outcomes

Primary

MeasureTime frameDescription
Episodic memory performance - learning curve0.25 hoursNumber of encoded words during the three consecutive immediate retrievals in the encoding phase
Episodic memory performance - delayed recall 120 min after encoding phaseNumber of remembered words in the delayed recall after a short delay at the day of the on-site visit
Episodic memory performance - delayed recall 21 day after on-site visitNumber of remembered words one day after learning

Secondary

MeasureTime frameDescription
Neurotransmitter levels0.5 hoursChanges in neurotransmitter levels (gamma-Aminobutyric acid (GABA) and glutamatergic metabolites (Glx) due to tDCS (comparing pre- and post-stimulation measurements in DLPFC)

Countries

Switzerland

Outcome results

None listed

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