Skip to main content
OpenTrials
Enrolling by Invitation

NCT Number: NCT07634133

The Impact of Omega-3 Fatty Acid Supplementation on the Composition of Erythrocyte Membranes

Therefore, the aim of our project will be to assess the impact of omega-3 fatty acid on the neuromuscular system (muscle tensomyography- TMG), the composition and fluidity of erythrocyte cell membranes, the lipid profile and the antioxidant status of the blood.

Enrolling by Invitation

Interested in participating?

Request Info

Key information

Conditions

Age range

18 year–60 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Academy of Physical Education in Katowice

Katowice, 40-065, Poland

About this study

The ability of skeletal muscles to generate force and resist fatigue is essential for athletic performance. Training adaptations within the neuromuscular system and skeletal muscles modulate the muscles' ability to produce force and resistance to fatigue. Much research has been conducted to determine the effects of dietary supplements on skeletal muscle adaptation to strength training (e.g., protein supplementation) and methods to support endurance performance (e.g., carbohydrate loading). However, limited research has been conducted to date on the effects of dietary supplements on the neuromuscular system.The research will focus on the effect of 4 and 8 weeks of supplementation with high doses of omega 3 fatty acids on the level of omega 3/omega6 fatty acids, the level of TRANS fatty acids and AA (arachidonic acid) fatty acid using a mixed diet. Additionally, we will examine the effect of this supplementation on the neuromuscular system (muscle tensomyography -TMG), the composition and fluidity of erythrocyte cell membranes, the lipid profile and the antioxidant status of the blood. The research will use innovative assumptions - high doses of omega 3 fatty acids. Additionally, a new laboratory tool will be used to assess the level of individual fatty acids (omega 3, omega 6) in the blood, the level of which shows or excludes latent inflammation in the body.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

**Inclusion Criteria:**

  • Male participants aged 20-40 years.
  • Apparently healthy individuals, as determined by medical history and self-reported health status.
  • Physically active, engaging in regular physical activity at least 3 times per week for the previous 6 months.
  • Following a mixed diet.
  • Willingness to maintain habitual dietary and physical activity patterns throughout the study.
  • Willingness to refrain from consuming dietary supplements other than those provided as part of the study.

**Exclusion Criteria:**

  • Current use of dietary supplements within 4 weeks prior to enrollment.
  • Following a low-carbohydrate, ketogenic, high-carbohydrate, vegetarian, or vegan diet.
  • Presence of gastrointestinal disorders affecting nutrient absorption, including irritable bowel syndrome, inflammatory bowel disease, celiac disease, or other clinically significant gastrointestinal conditions.
  • History of cardiovascular, metabolic, endocrine, hepatic, renal, neurological, or autoimmune diseases.
  • Current use of medications known to affect lipid metabolism, inflammation, antioxidant status, or cognitive function.
  • Known allergy or intolerance to study supplements or their ingredients.
  • Participation in another clinical trial within the previous 3 months.

Treatment and study plan

EPA/DHA supplements

Dietary Supplement

The supplement will be administered in a dose of 4 capsules twice a day for 4 weeks. Each capsule will contain 330mg EPA and 220mgDHA.

Other names: EPA/DHA supplementation, ALA supplementation, Placebo supplementation

ALA supplements

Dietary Supplement

The supplement will be administered in a dose of 4 capsules twice a day for 4 weeks. Daily dose will contain 3500mg ALA.

Placebo Supplements

Dietary Supplement

The supplement will be administered in a dose of 4 capsules twice a day for 4 weeks. One capsule will contain 550 mg of olive oil. The placebo will be matched to the supplement in appearance.

Primary outcomes

  1. Omega 3 index

    Time frame: 4-weeks

    The Omega-3 Index (%) determines the content of EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid) relative to total fatty acids in erythrocyte membranes. It is expressed as a percentage and reflects long-term fatty acid intake.

    Unit of Measure: %

Secondary outcomes

  1. Tensiomyography (TMG) Parameters

    Time frame: 4-weeks

    2a. Maximal Radial Displacement (Dm) Unit of Measure: mm 2b. Contraction Time (Tc) Unit of Measure: ms 2c. Delay Time (Td) Unit of Measure: ms 2d. Sustain Time (Ts) Unit of Measure: ms 2e. Half-Relaxation Time (Tr) Unit of Measure: ms Description: Muscle contractile properties assessed using tensiomyography (TMG-BMC system).

  2. Corsi Block-Tapping Test - Unweighted Block Span

    Time frame: 4-weeks

    Description: Maximum correctly reproduced sequence length in Corsi Block-Tapping Test.

    Unit of Measure: blocks

  3. Corsi Block-Tapping Test - Block Time

    Time frame: 4 weeks

    Description: Reaction time performance in visuospatial working memory assessed using Corsi Block-Tapping Test.

    Unit of Measure: ms

  4. Corsi Block-Tapping Test - Reverse Span Score

    Time frame: 4 weeks

    Description: Working memory performance assessed using reverse span condition of Corsi Block-Tapping Test.

    Unit of Measure: score

Other outcomes

  1. Total Antioxidant Status (TAS)

    Time frame: 4 weeks

    Description: Plasma total antioxidant status measured using Randox TAS kit.

    Unit of Measure: mmol/L

  2. Malondialdehyde (MDA) Concentration

    Time frame: 4 weeks

    Description: Plasma malondialdehyde concentration measured using thiobarbituric acid reactive substances method.

    Unit of Measure: nmol/mL

  3. Superoxide Dismutase (SOD) Activity

    Time frame: 4 weeks

    Description: Activity of superoxide dismutase in red blood cell lysates measured using Randox kits.

    Unit of Measure: U/g Hb

  4. Glutathione Peroxidase (GPx) Activity

    Time frame: 4 weeks

    Description: Activity of glutathione peroxidase in red blood cell lysates measured using Randox kits.

    Unit of Measure: U/g Hb

  5. Body Mass

    Time frame: 4 weeks

    Description: Body mass measured using multi-frequency bioelectrical impedance analysis (InBody 770).

    Unit of Measure: kg

  6. Body Fat Percentage

    Time frame: 4 weeks

    Description: Body fat percentage measured using multi-frequency bioelectrical impedance analysis (InBody 770).

    Unit of Measure: %

Sponsors and collaborators

Lead sponsor

The Jerzy Kukuczka Academy of Physical Education in Katowice

Other

Registry information

Official study title

The Impact of Omega-3 Fatty Acid Supplementation on the Composition of Erythrocyte and Neuromuscular System in Athletes

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jun 8, 2026
Registry last updated
Jun 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.