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tES Effects on Associative Memory Performance

Effects of Transcranial Electric Stimulation on Associative Memory Formation in Healthy Elderly Participants as Well as in Individuals With Memory Impairment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03351452
Enrollment
28
Registered
2017-11-22
Start date
2018-04-09
Completion date
2020-02-24
Last updated
2020-03-13

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

Conditions

Healthy, Mild Cognitive Impairment, Alzheimer Disease

Brief summary

Previous studies showed that transcranial electric stimulation (tES) applied over the prefrontal cortex improves cognitive performance in healthy elderly adults as well as in patients suffering from mild cognitive impairment or early Alzheimer's disease. Therefore, tES methods might be a useful intervention tool for patients suffering from memory impairment in early terms of the disease. The present study aims at establishing a connection between the stimulation-induced changes on associative memory performance and its underlying neurophysiological parameters. tES effects and their underlying mechanisms will be compared between healthy elderly controls and clinical study populations receiving either real or sham tES over the left ventrolateral prefrontal cortex during an associative memory task.

Interventions

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

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

DEVICEsham transcranial electric current stimulation

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

Sponsors

University of Bern
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Written informed consent * Non-smokers * Right-handedness * 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 * Skin diseases

Design outcomes

Primary

MeasureTime frameDescription
Performance on immediate cued recall task20 minNumber of correct responses on retrieval task of previously learned associative memory items
Performance on delayed cued recall task24 hoursNumber of correct responses on retrieval task of previously learned associative memory items

Secondary

MeasureTime frameDescription
task-dependent BOLD activity20 minMeasured with functional magnetic resonance imaging (fMRI)
resting-state BOLD activity10 minMeasured with functional magnetic resonance imaging (fMRI)

Other

MeasureTime frameDescription
Performance on cued recall taskfollow-up after 24 hoursNumber of correct responses on retrieval task of previously learned associative memory items
Performance on recognition taskfollow-up after 24 hoursNumber of correct responses on retrieval task of previously learned associative memory items

Countries

Switzerland

Outcome results

None listed

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