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NAD+ Oral Supplement Pilot Intervention in Adult Females

NAD+ Oral Supplement Pilot Intervention in Adult Females

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06579209
Enrollment
53
Registered
2024-08-30
Start date
2024-12-01
Completion date
2026-02-20
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Change, Inflammation, Neurodegenerative Diseases

Brief summary

The goal of this clinical trial is to learn whether Nicotinamide adenine dinucleotide (NAD+) can influence cognition and biomarkers in healthy, cognitively intact women aged 40-80. The main questions it aims to answer are: Will cognitive functioning change in response to NAD+? Will inflammatory markers and serum indicators of neurodegeneration change in response to NAD+? Researchers will compare individuals receiving NAD+ to those receiving placebo to see if the results differ. 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

Interventions

DIETARY_SUPPLEMENTTreatment

Participants will take a supplement for four weeks. The supplement will either be Nicotinamide adenine dinucleotide or a placebo.

OTHERPlacebo

Participants will take a supplement for four weeks. The supplement will either be Nicotinamide adenine dinucleotide or a placebo pill.

Sponsors

University of Rhode Island
Lead SponsorOTHER
National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Identify as Female * Have a BMI of 18.5 or above * Must be able to swallow tablets

Exclusion criteria

* Those who are pregnant, breastfeeding, or taking hormone medication

Design outcomes

Primary

MeasureTime frameDescription
Neurocognitionfour weeksNIH Toolkit Cognition Battery, Automated Neuropsychological Assessment Metrics
Neurodegenerative disease panelfour weeksBDNF, Cathespin D, MPO, PAI-1 (total), PDGF-AA, PDGF-AB/BB, RANTES, slCAM-1, sNCAM, sVCAM-1
Markers of systemic inflammationfour weeksGM-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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026