Summary

Eligibility
for people ages 18-35 (full criteria)
Healthy Volunteers
healthy people welcome
Location
at Los Angeles, California
Dates
study started
completion around
Principal Investigator
by Jeremy Swisher, MD

Description

Summary

This study is testing whether a special form of magnesium called magnesium L-threonate can help improve sleep quality, recovery, and physical performance in college athletes. Magnesium is important for muscle recovery and sleep, but many forms of it do not enter the brain well. Magnesium L-threonate is unique in that it can cross the blood-brain barrier and may improve deep and REM sleep, heart rate variability, and brain recovery.

In this study, healthy UCLA varsity athletes aged 18 to 35 will be randomly assigned to take either magnesium L-threonate or a placebo each evening for 4 weeks. They will wear a WHOOP strap to track sleep, recovery, and heart rate data. Performance tests including jump height, grip strength, and reaction time will be completed before and after the 4-week period.

This study will help researchers determine if this supplement can support recovery and training in athletes and whether wearable technology can help monitor these changes in real time.

Official Title

Effects of Magnesium L-Threonate on Sleep, Recovery, and Athletic Performance in UCLA Athletes: A Randomized, Placebo-Controlled Trial

Details

This is a randomized, placebo-controlled trial examining the effects of magnesium L-threonate (MgT) supplementation on sleep architecture, autonomic recovery, and physical performance in collegiate athletes. Magnesium is a critical mineral for neuromuscular and autonomic function, but common forms have limited central nervous system penetration. MgT crosses the blood-brain barrier and has been shown in non-athletic populations to improve sleep depth, REM sleep, and cognitive function. No prior studies have evaluated its effects in athletes.

Approximately 100 UCLA varsity athletes aged 18-35 will be randomized in a 1:1 ratio to receive 1 gram of MgT or placebo nightly for 4 weeks. Participants will wear a WHOOP strap to continuously monitor deep sleep, REM sleep, heart rate variability, resting heart rate, and recovery score. Daily surveys will track subjective sleep quality, recovery, and for female athletes, menstrual phase and symptoms. Performance outcomes including countermovement jump height, handgrip strength, and light-based reaction time will be measured before and after the intervention.

Primary outcomes include objective changes in sleep stages and HRV. Secondary outcomes include changes in physical performance and subjective recovery. This study will provide insight into whether brain-targeted magnesium supplementation can enhance recovery and performance in an athletic population.

Keywords

Recovery of Function (G11.427.698.620), Athletic Performance, Heart Rate Variability (HRV), Magnesium L-Threonate, Sleep Quality, WHOOP, Athlete Recovery, HRV, NCAA Athletes, Sports Medicine, Wearable Technology

Eligibility

You can join if…

Open to people ages 18-35

  • • Age 18-35 years
    • Current UCLA varsity athlete (any sport)
    • Actively training or competing during the study period
    • Willing to wear a WHOOP strap continuously for 4 weeks
    • Willing to ingest a nightly capsule for 4 weeks
    • Able to provide informed consent and comply with study procedures

You CAN'T join if...

  • • Current use of magnesium supplements or investigational drugs
    • Use of prescription or over-the-counter sleep medications
    • Diagnosed sleep disorder (e.g., insomnia, sleep apnea)
    • Major medical condition limiting training or participation
    • Pregnancy or breastfeeding
    • Known history of chronic kidney or liver disease
    • Allergy or intolerance to magnesium
    • Inability to comply with study procedures (e.g., wearing WHOOP or completing surveys)

Location

  • UCLA
    Los Angeles California 90094 United States

Lead Scientist at UCLA

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Los Angeles
ID
NCT07015047
Study Type
Interventional
Participants
Expecting 100 study participants
Last Updated