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Effects of Vitamin D Supplementation on Strength, Bone Density, and Injury Risk in Collegiate Athletes

Early Phase 1
Completed
Conditions
Vitamin D Deficiency
Interventions
Drug: Vitamin D 10000 UNT
Drug: Vitamin D 5000 UNT
Registration Number
NCT03151174
Lead Sponsor
Virginia Polytechnic Institute and State University
Brief Summary

The goal of this study is to determine whether Vitamin D supplementation improves strength and bone density, and reduces the risk of injury in collegiate athletes.

Detailed Description

Vitamin D is a hormone that is important for bone and muscle health. As such, not having enough vitamin D in your body is associated with increased risk of injury and reduced health and athletic performance. It is often recommended that individuals who have low levels of vitamin D take vitamin D supplements. However, the effects of vitamin D supplementation on health and strength gains in collegiate athletes are not known. The goal of this study is to determine whether vitamin D supplementation increases strength and bone density, while reducing the risk of injury in collegiate athletes. Fasting vitamin D concentrations will be measured and athletes will be supplemented daily with Vitamin D for 8-12 weeks. The amount of supplementation will depend on whether the athlete is categorized as sufficient (\>30ng/ml), insufficient (20-35ng/ml), or deficient (\<20ng/ml). Vitamin D concentrations, strength, bone density, and injury risk will be assessed before and after the intervention period.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
68
Inclusion Criteria
  • athlete for a sanctioned Virginia Tech sport
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Exclusion Criteria
  • pregnant or trying to become pregnant, currently taking vitamin D (>600IU/day), calcium (>1000mg/dl), taking any performance enhancing supplements (example, creatine), or any other medication or nutritional supplements that might influence the study variables, cardiac or thyroid problems, have diabetes, or epilepsy
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Vitamin D - 10000IUVitamin D 10000 UNTThese individuals have been categorized as Vitamin D deficient and will receive 10000IU of Vitamin D per day.
Vitamin D - 5000IUVitamin D 5000 UNTThese individuals have been categorized as Vitamin D insufficient and will receive 5000IU of Vitamin D per day.
Primary Outcome Measures
NameTimeMethod
StrengthUp to 12 weeks

Overall strength assessed via maximal strength testing. The specific tests may include the following, 1) one repetition max bench press (lbs) -, 2) one repetition max squat (lbs), 3) vertical jump test (feet), 4) broad jump test (feet), 5) dead lifts (lbs and repetition), 6) pull ups (repetition), 7) dips (repetition), and 8) shuttle time (test involving repeated sprints to and from marked points or lines - minutes/ seconds).

Secondary Outcome Measures
NameTimeMethod
Injury OccurenceEvery week for up to 12 weeks

New and current Injuries including bone breaks, muscle strains and sprains will be tracked via a questionnaire that will be filled out weekly. Subjects will report whether they had an injury, where the injury occurred on the body, the type of injury, as well as the date/ time of the injury and how the injury occurred.

Number of injury

Femur Bone DensityUp to 12 weeks

Bone Density will be assessed in spine using Dual Energy X-ray Absorptiometry. T-scores will be determined.

Spine Bone DensityUp to 12 weeks

Bone Density will be assessed in the hip (proximal femur) using Dual Energy X-ray Absorptiometry. T-scores will be determined.

Trial Locations

Locations (1)

Virginia Tech

🇺🇸

Blacksburg, Virginia, United States

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