A Study Evaluating the Use of 31P MRS to Assess Brain NAD+ Levels as Compared to Nicotinamide Riboside Supplementation in Healthy Current and Former Collegiate Athletes
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 15-006870
- Minneapolis, Minnesota: 15-006870
NCT ID: NCT02721537
Sponsor Protocol Number: 15-006870
About this study
The purpose of this study is to determine if nicotinamide riboside (750 mg/day for 12 weeks) can affect the levels of NAD+ in the brain as measured by 31P MRS.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
- Current and former adult collegiate male and female athletes.
- Aged 18 years and older.
- Participants in football, rugby, soccer, hockey, lacrosse, and/or volleyball.
- Note: “Former collegiate athletes” is defined as having competed in the applicable sports within the previous two years.
- Body mass index (estimated based on height and weight) from 20 to 37.
- Agree to maintain current level of physical activity throughout the study
- Willing and able to provide written informed consent.
- Willing and able to ingest the test substance.
- Willing and able to comply with study instructions.
- Not pregnant or breast feeding
Exclusion Criteria:
- Presence of prolonged (more than 5 minutes) loss of consciousness.
- Normal contraindications to MRI procedures, including but not limited to implanted medical (metal, magnetic, or electronic) devices or having metal objects or pacemakers.
- History of epilepsy.
- History of more than 3 concussions.
- History of headache preceding concussions.
- History of complex spine and/or skull traumas.
- History of depression preceding concussions.
- History of intracranial bleeding or strokes.
- History of post-traumatic seizures.
- History of developmental delay.
- History of ADHD.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Rochester, Minn.
Mayo Clinic principal investigator Brent Bauer, M.D. |
Closed for enrollment |
|
Minneapolis, Minn.
Mayo Clinic principal investigator Brent Bauer, M.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available