Use of 31P MRS to Assess Brain NAD+ in Healthy Current and Former Collegiate Athletes
Status: | Recruiting |
---|---|
Conditions: | Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/2/2019 |
Start Date: | September 2016 |
End Date: | June 2020 |
Contact: | Stephanie Lindeen, RN |
Email: | athletesstudy@mayo.edu |
Phone: | 507-284-4799 |
Use of 31P MRS to Assess Brain NAD+ in Healthy Current and Former Collegiate Athletes and a Comparison of the Effect of Nicotinamide Riboside Supplementation on Brain NAD+ Levels
Can nicotinamide riboside (750 mg/day for 12 weeks) affect the levels of NAD+ in the brain as
measured by 31P MRS?
measured by 31P MRS?
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.
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.
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:
- 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
We found this trial at
2
sites
Minneapolis, Minnesota 55455
Principal Investigator: Xiao-Hong Zhu, Ph.D.
Phone: 612-624-9926
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Rochester, Minnesota 55905
Principal Investigator: Brent A Bauer, MD
Phone: 507-293-2740
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