NAD+ Oral Supplement Pilot Intervention in Adult Females
- Conditions
- Cognitive ChangeInflammationNeurodegenerative Diseases
- Registration Number
- NCT06579209
- Lead Sponsor
- University of Rhode Island
- Brief Summary
The goal of this clinical trial is to learn if Nicotinamide adenine dinucleotide (NAD+) can influence cognition and biomarkers in healthy, cognitively intact women who identify as Latina and are between the ages of 40-80. The main questions it aims to answer are:
Will executive function change in response to NAD+? Will inflammatory markers and serum indicators of neurodegeneration change in response to NAD+? Researchers will compare individuals receiving the NAD+ to see if the results differ from those receiving the placebo.
Participants will:
Complete an online questionnaire, Visit the lab for computerized cognitive testing and a blood draw, Take NAD+ or a placebo every day for 4 weeks, Visit the lab for computerized cognitive testing and a blood draw
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 50
- Identify as Latina, have three or more adverse childhood experiences, and a BMI of 18.5 or above
- Those who are taking hormone medication, pregnant or breastfeeding
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Neurocognition four weeks NIH Toolkit Cognition Battery, Automated Neuropsychological Assessment Metrics
Neurodegenerative disease panel four weeks BDNF, Cathespin D, MPO, PAI-1 (total), PDGF-AA, PDGF-AB/BB, RANTES, slCAM-1, sNCAM, sVCAM-1
Markers of systemic inflammation four weeks GM-CSF, IFNγ, IL-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12p70, IL-13, IL-17A, IL-23, TNFα
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
University of Rhode Island
🇺🇸Kingston, Rhode Island, United States
Independence Square, University of Rhode Island
🇺🇸Pawtucket, Rhode Island, United States