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临床试验/NCT05277727
NCT05277727已完成不适用

Impact of a Novel Marine Algae Supplement on the Inflammatory and Immune Response After High Intensity Exercise

Marinova Pty Ltd2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2022年1月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
2
主要终点
Changes in interleukin-6

研究概览

简要总结

This double-blinded, randomized, placebo-controlled, cross-over study is designed to evaluate the potential effects of a fucoidan supplement on the inflammatory and immune responses following high intensity exercise.

详细描述

Inflammation is an innate immune response to tissue damage as a means of increasing blood flow to a specific area to facilitate repair, and is associated with the movement of fluid, plasma proteins, and immune cells from the circulation to the site of injury. The inflammatory process is initiated by cytokines which attract specific immune cells, such as monocytes, lymphocytes, neutrophils, and eosinophils, to the damaged tissue. Chronic exercise has been found to reduce inflammation and bolster immune system function; however, acute exercise has been shown to increase inflammatory response. Cytokine secretion and concentrations as well as leukocyte activation following exercise appear to increase in proportion to exercise intensity. Therefore, on an acute basis, high intensity exercise may cause immunosuppression and increased inflammation. High degrees of muscle damage and inflammation post-exercise result in decrements in muscle strength and range of motion, increased delayed onset muscle soreness (DOMS) and swelling, as well as the efflux of myocellular proteins and enzymes, including creatine kinase (CK). Therefore, post-exercise nutritional supplementation for individuals participating in high intensity exercise may be beneficial to modulate exercise-associated immune function and reduce inflammation.

Fucoidans are fucose-rich sulfated carbohydrates found in brown marine algae and have been shown to play a role in immune modulation as well as inflammation. In fact, fucoidans have been shown to inhibit neutrophil infiltration and attenuate levels of pro-inflammatory cytokines. More research is warranted to determine the effects of supplementation with fucoidans to reduce inflammation following high intensity exercise. Therefore, this double-blinded, randomized, placebo-controlled, cross-over design study will be conducted to further understand these effects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

Both subjects and study research team will not be aware of their assigned conditions.

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Fully vaccinated against COVID-19 (participant has received their final dose at least one month prior to the screening visit).
  • Individuals who regularly exercise as per physical activity guidelines for Americans10 [structured exercise for a minimum of 150 cumulative minutes per week (low end) to 500 cumulative minutes of exercise per week (high-end)] and willing to maintain the same level of physical activity throughout the study period.
  • Healthy individuals between 18 to 40 years of age (inclusive).
  • Individuals with BMI in the range of 18.5-34.9 (inclusive).
  • Good health as determined by medical history and cleared for exercise as assessed by the PI.
  • Male and female participants of reproductive potential should be willing to use double-barrier to avoid pregnancy and sexually transmitted infection (STI) during the study period.
  • Provide signed and dated informed consent form.
  • Willing and able to comply with the protocol.

排除标准

  • Participants with existing musculoskeletal injuries that would prevent full participation.
  • History of clinically significant cardiovascular, respiratory, renal, cerebrovascular, metabolic, pulmonary, gastrointestinal, neurological, hematological, autoimmune, lymphatic, psychiatric, hepatobiliary, or endocrine disorders, including individuals with Type I or Type II diabetes, or other clinically significant medical condition that, in the opinion of the PI, may preclude safe study participation.
  • Females who are pregnant, lactating, or planning on becoming pregnant during the course of the study.
  • Participants using blood thinning medications or supplements.
  • Participants having a known sensitivity or allergy to any of the study products or their excipients.
  • Participating or has participated in another research study in which another study product has been consumed within 30 days prior to the study screening visit.
  • Participants with current or past medical history of long-term COVID-19 symptoms (remained symptomatic for at least 2 weeks or more).
  • Professional athletes, collegiate athletes, competitive body builders, or those who compete at the elite category within their sport.
  • Participant having any condition or abnormality that, in the opinion of the investigator, would compromise the safety of the participant or the quality of the study data.

结局指标

主要结局

Changes in interleukin-6

时间窗: After 14 days of supplementation

To determine if the TP has an impact on interleukin-6 compared to placebo

Changes in T cell

时间窗: After 14 days of supplementation

Monitor changes in T cell subset CD4 and CD8 for TP compared to placebo

Changes in interleukin-1B

时间窗: After 14 days of supplementation

To determine if the TP has an impact on interleukin-1B compared to placebo

Changes in interleukin-10

时间窗: After 14 days of supplementation

To determine if the TP has an impact on interleukin-10 compared to placebo

Changes in CBC panel

时间窗: After 14 days of supplementation

Changes in CBC panel (absolute counts of Neutrophils, Lymphocytes, Monocytes, Eosinophils, and Basophils) compared between two study arms to determine if the TP has an impact compared to placebo

Changes in B cell

时间窗: After 14 days of supplementation

Monitor changes in B cell subset CD4 and CD8 for TP compared to placebo

次要结局

  • Safety Outcome Measures(After 14 days of supplementation)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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