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CompletedNCT02721537TRMC-004Updated Aug 3, 2022

Use of 31P MRS to Assess Brain NAD+ in Healthy Current and Former Collegiate Athletes

An interventional study of Nicotinamide Riboside and Matching placebo in Concussion, Mild, sponsored by Mayo Clinic. Completed at 2 sites in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-08-03.

Sponsored by Mayo Clinic · Not applicable, Interventional, and Screening

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Can nicotinamide riboside (750 mg/day for 12 weeks) affect the levels of NAD+ in the brain as measured by 31P MRS?

Read the detailed description

Healthy collegiate athletes (football, soccer, rugby, hockey, and volleyball) will take Nicotinamide Riboside (NR) or placebo twice daily for 84 days. Pre- and post-intervention evaluations include physical assessment, blood tests for safety and toxicity monitoring, blood tests for biomarkers, neurologic testing, quality of life questionnaires, and the 31P MRI exam.

02

Conditions studied

  • Concussion, Mild

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Keywords

  • Brain Nicotinamide Adenine Dinucleotide (NAD+)
  • Adenosine Triphosphate (ATP) Depletion
  • Polyadenosine Diphosphate-Ribosepolymerase (PARP) Activation
03

In context

Brain Concussion

550 studies on the registry are indexed under Brain Concussion; 154 are open to participants now.

This study's enrollment of 30 is below the median of 64 across 376 interventional studies indexed under Brain Concussion.

Browse Brain Concussion studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,263 studies on the registry; 670 are open to participants now.

Of its 450 completed or terminated interventional studies of FDA-regulated products, 318 (71%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult current and former (within 2 years) collegiate athletes (football, rugby, soccer, hockey, and volleyball)
  • Body mass index (estimated based on height and weight) from 23 to 37
  • Willing to provide informed consent, ingest test substance, and provide blood specimens
  • Willing to comply with study instructions and maintain current level of physical activity throughout the study

Exclusion criteria

Exclusion Criteria:

  • History of loss of consciousness of more than 5 minutes
  • Contraindications to Magnetic Resonance Imaging (MRI), such as implanted medical devices, metal objects, or pacemakers
  • History of epilepsy
  • History of more than 3 concussions
  • History of headache preceding a concussion
  • History of depression preceding a concussion
  • History of developmental delays or Attention Deficit Hyperactivity Disorder (ADHD)
  • History of post-traumatic seizures
  • History of complex spine and/or skull trauma
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
30 participants (actual)

Study arms

  • Active comparator
    Arm A: Healthy Collegiate Athletes

    Healthy collegiate athletes will take active Nicotinamide Riboside

    Dietary Supplement: Nicotinamide Riboside

  • Placebo comparator
    Arm B: Healthy Collegiate Athletes

    Healthy collegiate athletes will take a matching placebo

    Other: Matching placebo

Interventions

  • Dietary supplementNicotinamide Riboside

    Three capsules, twice per day for 84 days

    Also known as: Niagen

  • OtherMatching placebo

    Three matching capsules, twice per day for 84 days

06

What researchers measure

Primary outcomes

  1. Change in brain NAD+ levels

    As measured by 31P MRI

    Time frame: baseline, day 84

07

Study locations

2 sites
  • University of Minnesota Center for Magnetic Resonance Research
    Minneapolis, Minnesota 55455, United States
  • Mayo Clinic
    Rochester, Minnesota 55905, United States
08

References and documents

Individual participant data

Plan to share: Yes

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02721537
Lead sponsor
Mayo Clinic
Collaborators
University of Minnesota, Thorne HealthTech, Inc
Responsible party
Brent A. Bauer (M.D., Professor of Medicine, Mayo Clinic) — Principal investigator
First posted
Mar 29, 2016
Start date
Sep 2016
Primary completion
Aug 2022
Completion
Aug 2022
Last update
Aug 3, 2022

Study contacts

Brent A Bauer, MD
principal investigator · Mayo Clinic in Rochester, MN

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2022. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Nicotinamide-beta-riboside

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