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

2026年6月3日 更新者:Małgorzata Magdalena Michalczyk、The Jerzy Kukuczka Academy of Physical Education in Katowice

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

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.

研究概览

详细说明

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.

研究类型

介入性

注册 (估计的)

200

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Katowice、波兰、40-065
        • Academy of Physical Education in Katowice

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

是的

描述

**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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:诊断
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:AL (Alpha-linolenic acid) supplementation
Participants were randomly assigned to the ALA supplementation group. After 4 weeks of the supplementation, there was a 12-week wash-out period, after which the participants crossed over to the EPA /DHA group.
The supplement will be administered in a dose of 4 capsules twice a day for 4 weeks. Daily dose will contain 3500mg ALA.
实验性的:EPA (eicosapentaenoic acid)/DHA (docosahexaenoic acid) supplementation
Participants were randomly assigned to the EPA/DHA supplementation group. After 4 weeks of the supplementation, there was a 12-week wash-out period, after which the participants crossed over to the ALA group.
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.
其他名称:
  • 安慰剂补充
  • EPA/DHA supplementation
  • ALA supplementation
安慰剂比较:Placebo supplementation
Participants were randomly assigned to the Placebo group. After 4 weeks of the supplementation, there was a 12-week wash-out period, after which they repeated the placebo supplementation.
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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Omega 3 index
大体时间: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: %

4-weeks

次要结果测量

结果测量
措施说明
大体时间
Tensiomyography (TMG) Parameters
大体时间: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).
4-weeks
Corsi Block-Tapping Test - Unweighted Block Span
大体时间:4-weeks

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

Unit of Measure: blocks

4-weeks
Corsi Block-Tapping Test - Block Time
大体时间:4 weeks

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

Unit of Measure: ms

4 weeks
Corsi Block-Tapping Test - Reverse Span Score
大体时间:4 weeks

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

Unit of Measure: score

4 weeks

其他结果措施

结果测量
措施说明
大体时间
Total Antioxidant Status (TAS)
大体时间:4 weeks

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

Unit of Measure: mmol/L

4 weeks
Malondialdehyde (MDA) Concentration
大体时间:4 weeks

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

Unit of Measure: nmol/mL

4 weeks
Superoxide Dismutase (SOD) Activity
大体时间:4 weeks

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

Unit of Measure: U/g Hb

4 weeks
Glutathione Peroxidase (GPx) Activity
大体时间:4 weeks

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

Unit of Measure: U/g Hb

4 weeks
Body Mass
大体时间:4 weeks

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

Unit of Measure: kg

4 weeks
Body Fat Percentage
大体时间:4 weeks

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

Unit of Measure: %

4 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Małgorzata Magdalena Michalczyk, Phd、Institute of Sport Sciences, Jerzy Kukuczka Academy of Physical Education in Katowice

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年4月15日

初级完成 (实际的)

2026年2月25日

研究完成 (估计的)

2027年12月31日

研究注册日期

首次提交

2026年5月18日

首先提交符合 QC 标准的

2026年6月3日

首次发布 (实际的)

2026年6月8日

研究记录更新

最后更新发布 (实际的)

2026年6月8日

上次提交的符合 QC 标准的更新

2026年6月3日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • 4-II/2024
  • 2024/53/B/NZ7/02257 (其他赠款/资助编号:Narodowe Centrum Nauki)
  • RID/SP/0053/2024/01 (其他标识符:The Regional Initiative of Excellence programme)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

Anonymised data will be available upon reasonable request.

IPD 共享支持信息类型

  • 研究方案

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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