NCT07441122 · NOT YET RECRUITING

Enhancing Attention in Elderly Using a Brain-Computer-Interface

This trial is testing whether mindfulness meditation and gentle electrical brain stimulation (delivered through a headset while performing a memory task) can strengthen attention-related brain signals in older adults, including those with mild cognitive impairment. A computer reads brainwaves in real time and adjusts the intervention on the fly. This is a Phase NA study, meaning it is exploratory research focused on whether the approach shows measurable brain effects, not a late-stage proven treatment.

Eligibility criteria

Inclusion Criteria:
Younger adults:
* Good general health.
* Normal or corrected vision.
* no history of neurological/psychiatric disease
* ability to read and understand English
* ability to understand information and ability to give a free and informed consent
Older adults:
* Normal or corrected vision.
* Self-reports no current diagnosis of dementia.
* Ability to provide written/electronic, informed consent.
Exclusion Criteria:
Younger Adults:
* Neurological or psychiatric diseases that could be contraindicated for tACS (e.g., personal history of epilepsy/seizure brain damage, history of fainting, bipolar disorder, schizophrenia, current substance use disorder, etc.).
* Medications that elevate seizure threshold (e.g., stimulant medication, high dose bupropion).
* Factors hindering EEG acquisition and tACS delivery (e.g., skin infection, wounds, dermatitis, inability to access the scalp of the participant).
Older Adults:
* Neurological or psychiatric diseases that could be contraindicated for tACS (e.g., personal history of epilepsy/seizure brain damage, pacemakers, history of fainting, bipolar disorder, schizophrenia, current substance use disorder, etc.).
* Medications that elevate seizure threshold (e.g., stimulant medication, high dose bupropion).
* Factors hindering EEG acquisition and tACS delivery (e.g., skin infection, wounds, dermatitis, inability to access the scalp of the participant).
* Diagnosis of dementia.
* Do not have the capacity to provide informed consent.

The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.

Eligibility criteria as of 2026-06-09

View full record on ClinicalTrials.gov

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