About this trial
This project's main goal is to use state-of-the-art passive sensing techniques to identify digital biomarkers that relate to bioenergetic changes in the brain due to nicotinamide riboside supplementation in those with mild cognitive impairment and mild Alzheimer's dementia.
Eligibility criteria
Qualifiers
Ability of the participant and/or his/her legally authorized representative to understand the purpose and risks of the study, to provide signed and dated informed consent, and to authorize the use of confidential health information.
Ability to speak and read fluently in English
18-89 years old (inclusive)
Normal or corrected to normal hearing and vision
Disqualifiers
Current serious or unstable medical or neurological condition that could affect cognitive functioning, as determined by study clinician
Clinically unstable mood or anxiety disorder within 6 months prior to screening, as determined by study clinician
Lifetime history of psychotic disorder (i.e. Schizophrenia, Schizoaffective Disorder), as determined by study clinician
Diagnosis of a mitochondrial disorder
Trial design
Treatments tested in this trial
- Emerald Device Monitoring
Treatment groups
Sponsors and collaborators
Mclean Hospital
Lead sponsor
National Institute on Aging (NIA)
Collaborator