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The Effects of Antioxidant Supplementation on Multiple Endurance Race Performance, Physiology, and Recovery.

Applied Science & Performance Institute logo

Applied Science & Performance Institute

Status

Completed

Conditions

Muscle Strength
Muscle Damage
Resistance Training
Oxidative Stress
Body Composition

Treatments

Dietary Supplement: Oceanix
Other: Cross Training Course

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

Thirty active male and female athletes will be recruited for the study. Subjects will be examined at baseline for VO2max performance. Subjects will then be stratified and randomly divided equally (50% - 50%) into an Oceanix (supplemental) or placebo condition such that baseline VO2max match. Once randomization, subjects will be baseline tested for multiple measures of muscle force capacity, muscle soreness, immune function, and endocrine function. Upon completion of baseline testing, subjects will all complete a one-day, cross-training course in Tampa, Florida. The training course is known to be extremely vigorous and causes significant muscle damage. Subjects will then be retested for muscle function at 24, and 48 hours following the course. At 24- and 48-hours subjects will be asked to repeat a simulated time trial race. In this way, we will measure repeated race performance, recovery from intense exercise, muscle damage from exercise, and immune function during multiple races.

Enrollment

18 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Males and females age 18 to 45 years old
  • At least one year of cross training experience (i.e. 3 days/week)

Exclusion criteria

  • BMI of 30 or more kg/m²
  • Any allergies to fish, shellfish, algae, or seaweed are excluded from participation
  • Have any cardiovascular, metabolic, or endocrine disease
  • Undergone surgery that affects digestion and absorption
  • Smoking
  • Drink heavily (> 7 and > 14 drinks per week for women and men, respectively)
  • Women who are pregnant or planning to be pregnant
  • Taking medication to control blood pressure, lipids, and blood glucose
  • Have taken or currently taking anabolic-androgenic steroids

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

18 participants in 2 patient groups, including a placebo group

Placebo Group
Placebo Comparator group
Description:
Participants will engage in a one day, whole-body, cross-training course while consuming a visually identical placebo (25mg hydroxypropyl methylcellulose) 30 minutes prior to exercise on training days or with the first meal of the day on non-training days. Participants will then come in 24 and 48 hours post, cross-training course to be tested.
Treatment:
Other: Cross Training Course
Experimental Group
Experimental group
Description:
Participants will engage in a one day, whole-body, cross-training course while consuming the treatment condition (Oceanix™) 30 minutes prior to exercise on training days or with the first meal of the day on non-training days. Participants will then come in 24 and 48 hours post, cross-training course to be tested.
Treatment:
Dietary Supplement: Oceanix
Other: Cross Training Course

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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