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NCT05904132Recruiting

Individual Closed-Loop Neuromodulation Therapy for Alzheimer's Disease

Source: ClinicalTrials.gov · Last updated 14 Jul 2026

Brief summary (registry, in English)

The project is a placebo-controlled study that aims to use closed-loop transcranial alternating current stimulation (tACS) to study patients with symptoms of mild cognitive impairment which is likely due to Alzheimer's disease or another form of dementia (AD-MCI). Patients will undergo an EEG and complete some questionnaires and computer tasks during each study visit. The project has the following aims and hypotheses: 1.) To determine the impact of closed-loop 40 Hz tACS on the entrainment of natural gamma rhythms in patients with AD-MCI, 2.) To determine the impact of closed-loop 40 Hz tACS on cognitive performance in patients with AD-MCI, and 3.) To assess the relationship between baseline neurodegenerative burden and impact of tACS. \[exploratory\]

Status (registry)
Recruiting
Study type
Interventional
Enrollment
70 (estimated)
First submitted
22 May 2023
Start date
31 Jan 2025
Primary completion date
Jun 2027
Lead sponsor
Massachusetts General Hospital
NCT number
NCT05904132

What you commit to

  • Study type: Interventional
  • Planned participants: 70
  • From 31 Jan 2025 to the primary completion date, Jun 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Acute or decompensated active medical conditions, including cancer, cardiovascular disease, stroke, congestive heart failure
  • Active hematological, renal, pulmonary, endocrine or hepatic disorders
  • tACS contraindications (lesions in the scalp, history of seizures)

Other

  • Known presence of a structural brain lesion (e.g., tumor, cortical infarct)
  • Longstanding premorbid history (i.e., longer than 10 years) of alcohol or substance abuse with continuous abuse up to and including the time that the symptoms leading to clinical presentation developed

Who the study is looking for

  • Overall cognitive functional status consistent with amnesic MCI (CDR 0.5) likely due to AD (AD biomarker supported)
  • 50-80 years of age
  • English native speakers

Age in the registry: 50 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Massachusetts General Hospital
Coordinator of this site? Confirm its status
CharlestownUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.