Phase
Condition
Alzheimer's Disease
Dementia
Memory Loss
Treatment
Audiovisual stimulation VR system
Clinical Study ID
Ages 50-90 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria Mild AD/ MCI due to AD Participants:
Age between 50 - 90 years old.
A clinical diagnosis of Mild Cognitive Impairment due to Alzheimer's disease (confirmed by PET scan or CSF biomarkers) or Mild Alzheimer's disease
MoCA score of 18-25.
Willingness to sign informed consent document (if deemed to not have the capacity to sign the informed consent, a legally authorized representative will be asked to provide surrogate consent).
Sufficient visual and hearing ability.
Formal education of 8 or more years.
Native English speakers or demonstrated fluency in English (participant; and LAR as needed)
Inclusion Criteria Cognitively Healthy Participants:
Age between 50 - 90 years old.
A MoCA score above or equal to 26.
Willingness to sign informed consent document.
Sufficient visual and hearing ability.
Formal education of 8 or more years.
Native English speakers or demonstrated fluency in English (participant)
Exclusion Criteria Mild AD/ MCI due to AD Participants:
Previous exposure to monoclonal antibody medication (e.g., Lecanemab, Aducanumab).
Active treatment with Memantine within the past 30 days.
Initiation of acetylcholinesterase inhibitors within the past 30 days.
A history of seizure or epilepsy including family history of seizure or epilepsy.
A history of stroke.
A diagnosis of migraine headache.
History of alcohol use disorder within the past 2 years (DSM-V criteria).
Current or past history of any neurological disorder other than dementia.
Use of hearing aid device(s).
Any known blood pathogens or disorders.
Has any clinically significant medical disorder, condition, disease or clinically significant finding at screening that precludes participant's participation in study activities.
Pregnancy (Verbal confirmation).
Geriatric Depression Scale (GDS) >8
Exclusion Criteria Cognitively Healthy Participants:
Active treatment with Memantine within the past 30 days.
Initiation of treatment with acetylcholinesterase inhibitors (e.g., donepezil, rivastigmine and galantamine) within the past 30 days.
A history of seizure or epilepsy including family history of seizure or epilepsy.
A history of stroke.
A diagnosis of migraine headache.
History of alcohol use disorder within the past 2 years (DSM-V criteria).
Use of hearing aid device(s).
Any known blood pathogens or disorders.
A diagnosis of Alzheimer's disease and related dementias.
Has any clinically significant medical disorder, condition, disease or clinically significant finding at screening that precludes participant's participation in study activities.
Pregnancy (Verbal confirmation)
Geriatric Depression Scale (GDS) >8
Study Design
Study Description
Connect with a study center
The Sequoias Portola Valley
Portola Valley, California 18503
United StatesSuspended
Lakeview Institute of Clinical Research LLC
Leesburg, Florida 34748
United StatesActive - Recruiting
Urban Co-Works
Scranton, Pennsylvania 18503
United StatesSite Not Available
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