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Effect of Plant Omega-3 and Omega-6 Fatty Acids on Exercise Performance

Not Applicable
Conditions
Effect of Essential Fatty Acids on Exercise Performance
Interventions
Dietary Supplement: corn syrup
Dietary Supplement: Polyunsaturated fatty acid
Registration Number
NCT02654392
Lead Sponsor
University of Western Ontario, Canada
Brief Summary

Many studies in the past three decades have examined the beneficial effects of omega-3 polyunsaturated fatty acids in diet and supplementation. The effect of polyunsaturated fatty acids, specifically omega-3 and omega-6, on health have been well-studied but most of the study to date has been on animal not plant sources and much less is know about their effects on exercise performance. Additionally, while positive effects have been detected for sedentary populations or those that are at risk, well-trained athletes generally have not had established advantages in taking supplements for omega-3 and omega-6 oils. There is evidence that a specific ratio of omega-6 to omega-3 is most beneficial for the human body with regards to cardiovascular and mental health. In this study, participants randomized to either a plant supplement group (pureform omega; containing Flax, Evening Primrose, Sunflower, Coconut \& Pumpkin oils; Natural Product Number = 80050660) or placebo (isoenergetic sugar pills) will be subjected to both a time trial and a high intensity interval bout, where their performance and power output will be analyzed. Blood lactate and glucose concentration, as well as oxygen consumption and carbon dioxide production will also be examined to determine if there is a change in on fat oxidation after supplementation.

Detailed Description

Double-blind placebo controlled study with two groups: a PUFA supplemented group (over 5 weeks) and a placebo (corn syrup) group. Participants are matched for initial exercise performance and assigned to each of the two groups systematically so the initial group means are similar. This is done by ranking all individuals from highest to lowest and assigning the participant with the highest score randomly to the treatment group and the other to the placebo group. Then, for the next two individuals in ranking, the highest of the two is assigned to the placebo group and the other to the treatment group. This procedure is repeated for all participant pairs. Of course, this is done separately for men and women because on average the men have greater exercise performance scores.

Dosage is 3.8 capsules/70kg body mass (rounded to the nearest capsule; 1 capsule contains 369mg PUFA from Flax, Evening Primrose, Pumpkin, Sunflower, and Coconut oil; \<4 Calories) or isoenergetic placebo capsules (containing corn syrup) plus 2 capsules 20 minutes prior to exercise workouts. Eighteen recreationally active student volunteers (18-35 years old) will be recruited to complete 4 exercise tests: a cycle time trial (\~15 minutes), a cycle maximal power test (30 second Wingate test), a maximal aerobic power test (running treadmill test) plus a strength/endurance test (number of bench presses with 60 kg load) pre- and post 5 weeks of daily supplementation. There will an accommodation day pre-study where each participant is familiarized with the tests to be used. Each exercise test will be completed on a separate day with at least 48 hours between each test day due to the fatiguing nature of the testing.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
18
Inclusion Criteria
  • Healthy,
  • Recreationally active (defined as those who attend a gym or play sports about 2-3 times a week),
  • Non-pregnant student volunteers.
Exclusion Criteria
  • Participants cannot have taken omega-3 or other polyunsaturated fatty acid supplements or undergone any systematic exercise training in the past 3 months,
  • Have symptoms or take medication for respiratory, cardiovascular, metabolic, or neuromuscular disease
  • Injury limiting exercise ability
  • Use heart rate or blood pressure medications
  • Use any medications that have side effects for dizziness, lack of motor control, or slowed reaction time
  • Smoker

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placebocorn syrupThis group will receive isoenergetic carbohydrate (corn syrup) supplement daily for 5 weeks
Polyunsaturated fatty acid groupPolyunsaturated fatty acidThis group will receive a plant essential fatty acid food supplement, Pureform Omega® capsules made from Fax, Sunflower, Coconut, Evening Primrose, \& Pumpkin oils, containing a 2.5:1 omega-6 to omega-3 ratio (1.5 g per 70kg body mass plus an additional 0.5 g on exercise days)
Primary Outcome Measures
NameTimeMethod
change in cycle ergometer time trialat baseline and 5 weeks after supplementation

A 40 Km time trial test on a cycle ergometer will be conducted before and after a 5-week supplementation period

change in Aerobic capacity (VO2 max) testat baseline and 5 weeks after supplementation

Aerobic capacity will be quantified using an incremental running test on a treadmill. The workload will be increased by increasing the slope (simulating a hill) at a constant speed (6mph)

Change in Wingate Anaerobic Testat baseline and 5 weeks after supplementation

A 30 second intense effort on a cycle ergometer against a load equal to 9% of body mass. Peak power, mean power, total work and fatigue index will be recorded at the end of each sprint.

change in Strength/Endurance testat baseline and 5 weeks after supplementation

Number of bench presses completed (rounded to the nearest 1/2 lift) with a 60 kg load and a metromone for pacing control (30 lifts per minute) will be used and rating of perceived exertion (RPE) will be assessed immediately before and immediately after each exercise test using the Borg Scale (analog scale with verbal identifiers)

Secondary Outcome Measures
NameTimeMethod
change in Blood glucoseat baseline and 5 weeks after supplementation

Capillary blood samples (0.6 microlitres) will be collected before and after each exercise session under standard sterile condition via standard skin prick technique for the measurement of blood glucose content using a blood glucose analyzer (Free Style Lite)

change in Body compositionat baseline and 5 weeks after supplementation

Body composition will be measured by densitometry using air displacement plethysmography with a BodPod® (involves sitting comfortably in a chamber for about 2 minutes while the space the body takes up is measured) for the measurement of fat and fat-free mass

change in Blood lactateat baseline and 5 weeks after supplementation

Capillary blood samples (0.6 microlitres) will be collected before and after each exercise session under standard sterile condition via standard skin prick technique for the measurement of blood lactate content using a blood lactate analyzer (Lactate Scout+).

Trial Locations

Locations (1)

Exercise Nutrition Research Laboratory, Western University

🇨🇦

London, Ontario, Canada

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