Passive Sensor Identification of Digital Biomarkers to Assess Effects of Orally Administered Nicotinamide Riboside

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-89
SponsorMclean Hospital

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

40 Participants
are divided into 1 treatment group

Sponsors and collaborators

Mclean Hospital

Lead sponsor

National Institute on Aging (NIA)

Collaborator