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

NCT05245903

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Alzheimer Disease
  • Dementia Alzheimers
  • Dementia
  • Cognitive Impairment
  • Mild Cognitive Impairment
  • Neurodegenerative Diseases
  • Neurocognitive Disorders
  • Neurocognitive Dysfunction
  • Cognitive Dysfunction
  • Mental Disorder

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 to 89 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Mclean Hospital
Last updated on ClinicalTrials.gov
November 6, 2025

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Massachusetts · 1

  • McLean Hospital · Belmont, MA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.