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

Primary Purpose

Alzheimer Disease, Alzheimer Disease, Early Onset, Alzheimer Disease, Late Onset

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
GENUS device (Active Settings)
GENUS device (sham settings)
Sponsored by
Massachusetts Institute of Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer Disease focused on measuring Alzheimer's, Alzheimer, Alzheimer's disease, Light and Sound Stimulation, Tactile Stimulation

Eligibility Criteria

50 Years - 100 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Subjects may be enrolled into the study if they meet all of the following criteria: Subject is between the ages of 50 - 100. Subject must have mild Alzheimer's disease with a Mini Mental State Exam (MMSE) score of 19-26. Subject is willing to sign informed consent document. If subject is deemed to not have capacity to sign the informed consent, he/she will need a legally authorized representative to provide surrogate consent. Able to complete the 1st month of at home stimulation at their primary residence. If subjects plan to spend more than 1 week away from their primary residence during the trial, their inclusion must be assessed by the research team. Exclusion Criteria: Subjects who meet any of the following conditions will not be enrolled in the study: Subjects who do not have healthcare. Subjects who are currently taking amyloid reducing therapy. Subjects who have >3 microbleeds/microhemmorhages in their brain. Active treatment on a dosage of one or more psychiatric agents (e.g. antidepressants, antipsychotics, etc) for LESS THAN three months (a stable dose for greater than or equal to three months is ok). Subjects who are being treated with N-methyl-D-aspartate (NMDA) receptor antagonists (eg. Memantine). Subjects on medications that lower seizure threshold such as wellbutrin, ciprofloxacin, levofloxacin, etc. Subjects with history of seizure or epilepsy within the past 24 months. Subjects with clinically significant suicide risk and/or suicide attempt in the past 1 year. Subjects with behavioral problems such as aggression/agitation/impulsivity that might interfere with their ability to comply with protocol. Active treatment with one or more anti-epileptic agent. Subjects who have had a stroke within the past 24 months. Subjects who have had eye surgery in the last 3 months or are scheduled to have eye surgery in the next 6 months (during the study) Subjects diagnosed with migraine headache. Subjects who have an active implantable medical device including but not limited to implantable cardioverter defibrillator (ICD), deep brain stimulator (DBS), cardiac pacemaker, and/or sacral nerve stimulator. Subjects who have profound hearing or visual impairment. Subjects who have a life expectancy of less than 2 years. Subjects who are pregnant. Current or past history of any neurological disorder other than dementia, such as epilepsy, stroke, progressive neurologic disease (e.g. multiple sclerosis) or intracranial brain lesions; and history of previous neurosurgery or head trauma that resulted in residual neurologic impairment.

Sites / Locations

  • Massachusetts Institute of TechnologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Alzheimer's Active Arm

Alzheimer's Control Arm

Arm Description

Exposure to active sensory stimulation (40Hz) for 60 minutes daily for the length of the trial (6 months).

Exposure to control stimulation (sham) for 60 minutes daily for the length of the trial (6 months).

Outcomes

Primary Outcome Measures

Feasibility of gamma frequency stimulation as assessed by a change of gamma frequency waves during EEG
Feasibility of gamma frequency stimulation in subjects with AD will be assessed by analyzing the EEG data from each subject as they undergo gamma light, sound, and tactile stimulation. Investigators will look for a sign of change in gamma frequency waves and determine the percent of subjects who show this change. This change will be assessed through FFT analyses on the EEG data in MATLAB, which looks at the different frequencies that were present during the EEG session.
Baseline incidence of stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Mid-point incidence of stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Endpoint incidence of stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Change in stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Changes in functional brain connectivity as measured by changes in brain white matter on functional MRI scans
Exploratory measure to check if there are changes in functional brain connectivity after 6 months of daily treatment with the light and sound device. Diffusion tensor imaging (DTI) will be used to test the connectivity and blood flow of the brain by identifying major white matter tracts. This data will be collected at baseline, month 3, and month 6 for each subject, and change will be determined by comparing these timepoints.
Changes in functional brain connectivity as measured by changes in blood-oxygen-level-dependent (BOLD) signals on functional MRI scans
Exploratory measure to check if there are changes in functional brain connectivity after 6 months of daily treatment with the light and sound device. BOLD (blood-oxygen-level-dependent) imaging will be used to determine how regions are communicating and activating together via blood flow. This data will be collected at baseline, month 3, and month 6 for each subject, and change will be determined by comparing these timepoints.
Changes in gamma entrainment, as measured by the change in response to 40Hz frequency during EEG sessions
Exploratory measure to check if there are changes in gamma entrainment after months of daily treatment with the light and sound device. Gamma entrainment during light and sound stimulation will also be assessed using EEG and FFT analyses in MATLAB to determine the degree to which the brain is responding to the 40hz frequency. This data will be collected at baseline, month 3, and month 6 for each subject, and change will be determined by comparing these timepoints.
Changes in molecular biomarkers in AD as measured by RNA sequencing data, particularly those related to inflammation and amyloid levels
Exploratory measure to check if there are changes in molecular biomarkers of AD (based on RNA sequencing data) as a result of 6 months of daily treatment with the light and sound device. RNA information will be extracted from subjects' blood samples at the baseline and month 6 visits. RNA sequencing of this blood is included based on previous transcriptomic analysis of peripheral leukocytes that showed that inflammation-related genes are related to neurodegenerative disease such as AD. Change will be determined by comparing RNA sequencing data between baseline and month 6 (the beginning and end of the trial).

Secondary Outcome Measures

Changes in the microbiome as measured by fecal samples
At baseline and month 6, subjects will produce a fecal sample and hand it off to study staff for storage and sample processing using the QIAamp PowerFecal Pro DNA Kit (Qiagen). Data will then be analyzed using the Divisive Amplicon Denoising Algorithm 2 (DADA2) pipeline, which will provide gut microbial composition in the different experimental groups. Pipeline outputs involve principal component analyses, and a custom in-house script will be used to make statistical comparisons. Change will be assessed by comparing the fecal sample analyses between baseline and month 6.
Changes in cognitive performance as assessed by scores on an Alzheimer's cognitive testing battery
Exploratory measure to check if there is any change in cognitive performance as a result of 6 months of daily sessions with the light and sound device. Alzheimer's testing battery will be administered at baseline, month 3, and month 6 visits, and change will be determined by comparing cognitive performance (via standardized scores) at these three timepoints. These tests measure a variety of cognitive abilities, including attention, different types of memory, processing speed, visual acuity, and more.
Changes in sleep/wake patterns, as measured by actigraph watch analyses
Subjects will be expected to wear a GTX9 actigraph watch daily to record activity and sleep/wake patterns throughout the 6-months of the trial. This watch is like a regular wrist watch, but it records daily activity and patterns through light and movement. The subject will be given their watch ~2 weeks before the trial start-date, and they will bring it in with them at baseline, month 3, and month 6 visits so researchers can download their data to analyze their length and quality of sleep, as well as their other circadian rhythms and patterns throughout each day. Change will be assessed by comparing actigraph data between baseline, month 3, and month 6, as subject progress throughout the trial.

Full Information

First Posted
October 19, 2022
Last Updated
September 26, 2023
Sponsor
Massachusetts Institute of Technology
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1. Study Identification

Unique Protocol Identification Number
NCT05655195
Brief Title
Chronic Treatment of Alzheimer's Disease by Gamma Light and Sound Therapy
Official Title
Chronic Treatment of Alzheimer's Disease With Gamma Frequency Stimulation
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 14, 2022 (Actual)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
September 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Massachusetts Institute of Technology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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, 50 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 one additional year and completing an 18-month study visit. 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.
Detailed Description
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. Gamma waves are important for memory, and in patients with AD, there are fewer gamma waves in the brain. 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. The investigators also developed a vibrating device for humans that stimulates the brain at 40Hz via tactile stimulation. The investigators want to see if using these devices can prevent dementia in people who are at risk for developing Alzheimer's disease. The investigators are recruiting 50 participants who have been diagnosed with Alzheimer's disease to participate in this study. There will be a small cohort of 4 early-onset AD participants aged 50-65, and the rest will be diagnosed with typical AD and aged 65+. It will take place at the Massachusetts Institute of Technology in Cambridge, MA, and will last 6 months with 3 required visits to the institution: the first at baseline, the second at three months, and the last after six months. Visits will include blood tests, fecal samples, EEG (using light, sound, and tactile stimulation), MRI, memory and cognitive tests, and questionnaires to monitor progress. Participants will take home a gamma light and sound device to use daily as well as a "Fitbit" type of watch to wear to track sleep patterns. Half of the participants will receive sham treatment, meaning they will use the investigators' device but the light and sound will not be set at 40Hz. The other half will receive the same device but it will be set to stimulate the brain with 40Hz light and sound. Neither the participant nor the investigators will know whether the participant is receiving sham or active stimulation. Participants will use the device for six months at home, for 60 minutes each day when they are awake. After six months, participants will have the option of continuing in the study for one additional year, during which time they will be guaranteed the 40Hz active treatment, regardless of their original group assignment. For this additional year, participants will continue to use the device for 60 minutes every day, and they will come in for a final visit to MIT at the 18-month time point. The purpose of this study is to determine whether gamma entrainment through non-invasive 40Hz sensory stimulation is possible in those with AD, and whether functional connectivity in their brain and molecular biomarkers of AD will change after 6 months of daily treatment with the investigators' light and sound device. The treatment's impact on the microbiome, cognition, and daily sleep and activity will also be measured. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease, Alzheimer Disease, Early Onset, Alzheimer Disease, Late Onset, Alzheimer's Disease (Incl Subtypes), Alzheimer's, Alzheimer's Disease
Keywords
Alzheimer's, Alzheimer, Alzheimer's disease, Light and Sound Stimulation, Tactile Stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Alzheimer's Active Arm
Arm Type
Active Comparator
Arm Description
Exposure to active sensory stimulation (40Hz) for 60 minutes daily for the length of the trial (6 months).
Arm Title
Alzheimer's Control Arm
Arm Type
Sham Comparator
Arm Description
Exposure to control stimulation (sham) for 60 minutes daily for the length of the trial (6 months).
Intervention Type
Device
Intervention Name(s)
GENUS device (Active Settings)
Other Intervention Name(s)
Gamma Frequency Stimulation, Light and Sound Stimulation
Intervention Description
Participants in the active, experimental group will use the GENUS devices configured to active (40Hz) setting for 60 minutes daily for 6 months.
Intervention Type
Device
Intervention Name(s)
GENUS device (sham settings)
Other Intervention Name(s)
Gamma Frequency Stimulation, Light and Sound Stimulation
Intervention Description
Participants in the control group will use the GENUS devices configured to the sham settings for 60 minutes daily for 6 months.
Primary Outcome Measure Information:
Title
Feasibility of gamma frequency stimulation as assessed by a change of gamma frequency waves during EEG
Description
Feasibility of gamma frequency stimulation in subjects with AD will be assessed by analyzing the EEG data from each subject as they undergo gamma light, sound, and tactile stimulation. Investigators will look for a sign of change in gamma frequency waves and determine the percent of subjects who show this change. This change will be assessed through FFT analyses on the EEG data in MATLAB, which looks at the different frequencies that were present during the EEG session.
Time Frame
Immediately after completing the stimulation at baseline, month 3, and month 6 visits
Title
Baseline incidence of stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Description
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Time Frame
Immediately after the completion of the stimulation at baseline.
Title
Mid-point incidence of stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Description
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Time Frame
Immediately after the completion of the stimulation at Month 3.
Title
Endpoint incidence of stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Description
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Time Frame
Immediately after the completion of the stimulation at the end of the trial- Month 6 timepoints.
Title
Change in stimulation-related adverse symptoms and side effects as assessed by post-stimulation questionnaires
Description
Tolerability and safety of gamma frequency stimulation will be assessed by using a questionnaire asking for the subjects' overall experience with the stimulation and denoting any adverse effects. Subjects will be asked specifically about headaches, light headedness, nausea, dizziness, dry eye, eye strain, light sensitivity, ringing in ears, and any other symptoms they are experiencing.
Time Frame
During weekly phone calls throughout the 6-month trial period
Title
Changes in functional brain connectivity as measured by changes in brain white matter on functional MRI scans
Description
Exploratory measure to check if there are changes in functional brain connectivity after 6 months of daily treatment with the light and sound device. Diffusion tensor imaging (DTI) will be used to test the connectivity and blood flow of the brain by identifying major white matter tracts. This data will be collected at baseline, month 3, and month 6 for each subject, and change will be determined by comparing these timepoints.
Time Frame
At baseline, month 3, and month 6 visits during MRI sessions
Title
Changes in functional brain connectivity as measured by changes in blood-oxygen-level-dependent (BOLD) signals on functional MRI scans
Description
Exploratory measure to check if there are changes in functional brain connectivity after 6 months of daily treatment with the light and sound device. BOLD (blood-oxygen-level-dependent) imaging will be used to determine how regions are communicating and activating together via blood flow. This data will be collected at baseline, month 3, and month 6 for each subject, and change will be determined by comparing these timepoints.
Time Frame
At baseline, month 3, and month 6 visits during MRI sessions
Title
Changes in gamma entrainment, as measured by the change in response to 40Hz frequency during EEG sessions
Description
Exploratory measure to check if there are changes in gamma entrainment after months of daily treatment with the light and sound device. Gamma entrainment during light and sound stimulation will also be assessed using EEG and FFT analyses in MATLAB to determine the degree to which the brain is responding to the 40hz frequency. This data will be collected at baseline, month 3, and month 6 for each subject, and change will be determined by comparing these timepoints.
Time Frame
At baseline, month 3, and month 6 visits during EEG sessions
Title
Changes in molecular biomarkers in AD as measured by RNA sequencing data, particularly those related to inflammation and amyloid levels
Description
Exploratory measure to check if there are changes in molecular biomarkers of AD (based on RNA sequencing data) as a result of 6 months of daily treatment with the light and sound device. RNA information will be extracted from subjects' blood samples at the baseline and month 6 visits. RNA sequencing of this blood is included based on previous transcriptomic analysis of peripheral leukocytes that showed that inflammation-related genes are related to neurodegenerative disease such as AD. Change will be determined by comparing RNA sequencing data between baseline and month 6 (the beginning and end of the trial).
Time Frame
Immediately after blood draw at baseline and month 6 visits
Secondary Outcome Measure Information:
Title
Changes in the microbiome as measured by fecal samples
Description
At baseline and month 6, subjects will produce a fecal sample and hand it off to study staff for storage and sample processing using the QIAamp PowerFecal Pro DNA Kit (Qiagen). Data will then be analyzed using the Divisive Amplicon Denoising Algorithm 2 (DADA2) pipeline, which will provide gut microbial composition in the different experimental groups. Pipeline outputs involve principal component analyses, and a custom in-house script will be used to make statistical comparisons. Change will be assessed by comparing the fecal sample analyses between baseline and month 6.
Time Frame
Immediately after fecal sample collection at baseline and month 6
Title
Changes in cognitive performance as assessed by scores on an Alzheimer's cognitive testing battery
Description
Exploratory measure to check if there is any change in cognitive performance as a result of 6 months of daily sessions with the light and sound device. Alzheimer's testing battery will be administered at baseline, month 3, and month 6 visits, and change will be determined by comparing cognitive performance (via standardized scores) at these three timepoints. These tests measure a variety of cognitive abilities, including attention, different types of memory, processing speed, visual acuity, and more.
Time Frame
Immediately after completion of cognitive batteries at baseline, month 3, and month 6 Visits
Title
Changes in sleep/wake patterns, as measured by actigraph watch analyses
Description
Subjects will be expected to wear a GTX9 actigraph watch daily to record activity and sleep/wake patterns throughout the 6-months of the trial. This watch is like a regular wrist watch, but it records daily activity and patterns through light and movement. The subject will be given their watch ~2 weeks before the trial start-date, and they will bring it in with them at baseline, month 3, and month 6 visits so researchers can download their data to analyze their length and quality of sleep, as well as their other circadian rhythms and patterns throughout each day. Change will be assessed by comparing actigraph data between baseline, month 3, and month 6, as subject progress throughout the trial.
Time Frame
Immediately after actigraph data download at baseline, month 3, and month 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects may be enrolled into the study if they meet all of the following criteria: Subject is between the ages of 50 - 100. Subject must have mild Alzheimer's disease with a Mini Mental State Exam (MMSE) score of 19-26. Subject is willing to sign informed consent document. If subject is deemed to not have capacity to sign the informed consent, he/she will need a legally authorized representative to provide surrogate consent. Able to complete the 1st month of at home stimulation at their primary residence. If subjects plan to spend more than 1 week away from their primary residence during the trial, their inclusion must be assessed by the research team. Exclusion Criteria: Subjects who meet any of the following conditions will not be enrolled in the study: Subjects who do not have healthcare. Subjects who are currently taking amyloid reducing therapy. Subjects who have >3 microbleeds/microhemmorhages in their brain. Active treatment on a dosage of one or more psychiatric agents (e.g. antidepressants, antipsychotics, etc) for LESS THAN three months (a stable dose for greater than or equal to three months is ok). Subjects who are being treated with N-methyl-D-aspartate (NMDA) receptor antagonists (eg. Memantine). Subjects on medications that lower seizure threshold such as wellbutrin, ciprofloxacin, levofloxacin, etc. Subjects with history of seizure or epilepsy within the past 24 months. Subjects with clinically significant suicide risk and/or suicide attempt in the past 1 year. Subjects with behavioral problems such as aggression/agitation/impulsivity that might interfere with their ability to comply with protocol. Active treatment with one or more anti-epileptic agent. Subjects who have had a stroke within the past 24 months. Subjects who have had eye surgery in the last 3 months or are scheduled to have eye surgery in the next 6 months (during the study) Subjects diagnosed with migraine headache. Subjects who have an active implantable medical device including but not limited to implantable cardioverter defibrillator (ICD), deep brain stimulator (DBS), cardiac pacemaker, and/or sacral nerve stimulator. Subjects who have profound hearing or visual impairment. Subjects who have a life expectancy of less than 2 years. Subjects who are pregnant. Current or past history of any neurological disorder other than dementia, such as epilepsy, stroke, progressive neurologic disease (e.g. multiple sclerosis) or intracranial brain lesions; and history of previous neurosurgery or head trauma that resulted in residual neurologic impairment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gabrielle De Weck, BS
Phone
617-258-7723
Email
gdeweck@mit.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Megan Colburn, MS
Phone
617-258-7723
Email
mcolburn@mit.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Li Huei Tsai, PhD
Organizational Affiliation
Massachusetts Institute of Technology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts Institute of Technology
City
Cambridge
State/Province
Massachusetts
ZIP/Postal Code
02142
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabrielle De Weck, BS
Phone
617-258-7723
Email
gdeweck@mit.edu
First Name & Middle Initial & Last Name & Degree
Megan Colburn, MS
Phone
617-258-7723
Email
mcolburn@mit.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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

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