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tDCS of the Left dlPFC: Effects on Information Processing

Not Applicable
Recruiting
Conditions
Healthy
Registration Number
NCT07168031
Lead Sponsor
University of Bern
Brief Summary

This study investigates how a non-invasive form of brain stimulation, called transcranial direct current stimulation (tDCS), affects brain activity and information processing in younger and older adults. The stimulation uses a very weak electrical current applied through electrodes placed on the scalp. This method is safe and widely used in research to study brain function.

Participants will complete computer-based tasks while receiving either active brain stimulation or a placebo (sham) stimulation. The task is designed to engage specific mental processes so that the investigators can study how the brain responds under different conditions. Brain activity will be measured using magnetic resonance imaging (MRI), both while participants perform the tasks and while they are resting.

The study will compare healthy younger (ages 20-40) and older (ages 60-80) adults to explore whether age influences how the brain responds to stimulation. By examining patterns of brain activation and connectivity, the investigators aim to better understand how tDCS can modulate cognitive processing across the adult lifespan.

The hypothesis is that applying tDCS to the left dorsolateral prefrontal cortex will change patterns of brain activity related to cognitive processing, and that these changes may differ between younger and older adults. This knowledge could help inform future research into brain stimulation techniques in different age groups.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
196
Inclusion Criteria
  • Healthy younger adults (ages 20-40) or healthy older adults (ages 60-80)
  • Normal or corrected-to-normal vision and hearing
  • Right-handed (for consistency in brain stimulation)
  • Able to give written informed consent and comply with study procedures
Exclusion Criteria
  • History of neurological or psychiatric disorders
  • Current use of medications that affect the central nervous system
  • Metal implants, pacemakers, or other contraindications for MRI or tDCS
  • History of seizures or epilepsy
  • Pregnancy
  • Participation in another brain stimulation study within the last 3 months
  • Any condition judged by investigators to interfere with safe participation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Task AccuracyDuring the intervention

Accuracy in responses during an information processing task, measured as the proportion of correct responses.

Task-Related Brain ActivationDuring the intervention

Changes in blood-oxygen-level-dependent (BOLD) signal during the information processing task, measured using fMRI.

Resting-State Functional ConnectivityImmediately before and after the intervention

Changes in functional connectivity between brain regions before and after stimulation, measured using resting-state fMRI.

Secondary Outcome Measures
NameTimeMethod
Task Reaction TimeDuring the intervention

Time in milliseconds between stimulus presentation and participant response during the information processing task.

Trial Locations

Locations (1)

University of Bern, Department of Old Age Psychiatry and Psychotherapy

🇨🇭

Bern, Switzerland

University of Bern, Department of Old Age Psychiatry and Psychotherapy
🇨🇭Bern, Switzerland
Jessica Peter, Prof.
Contact
+41 58 630 89 03
jessica.peter@unibe.ch

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