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Study identifier: NCT05655195 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Chronic Treatment of Alzheimer's Disease by Gamma Light and Sound Therapy

Condition: Alzheimer Disease · Alzheimer Disease, Early Onset · Alzheimer Disease, Late Onset  ·  Sponsor: Massachusetts Institute of Technology

PhaseNA
Planned participants60
Who can joinAll sexes, 65 Years to 100 Years
Healthy volunteersYes

About this study

Alzheimer's disease (AD) is characterized by significant memory loss, toxic protein deposits amyloid and tau) in the brain, and changes in the gamma frequency band on EEG. The investigator's lab found that boosting gamma waves in AD mouse models using light and sound stimulation at 40Hz not only reduced amyloid and tau in the brain, but also improved memory. The investigators developed a light and sound device for humans that stimulates the brain at 40Hz that can be used safely at home. For the present study, 60 participants with mild Alzheimer's disease will be enrolled and will use this light and sound device at-home daily for 6-months. Investigators will measure changes in brain waves with EEG, blood biomarkers, the microbiome via fecal samples, functional and structural MRI scans, memory and cognitive testing, and questionnaires at 3 in-person visits throughout the study. After the 6-month time point, participants will have the option of continuing in the study for at least one year and completing yearly study visits. This study will provide critical insight into extended therapy involving non-invasive 40Hz sensory stimulation as a possible therapeutic strategy for mild to moderate Alzheimer's disease.

This description comes directly from the study's public registry record.

Talk to the study team

gamma wave  ·  617-258-7723  ·  gamma.wave@mit.edu

Ana Trisini Lipsanopoulos, BS  ·  617-258-7723  ·  anat13@mit.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Massachusetts Institute of TechnologyCambridge, Massachusetts, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05655195