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临床试验/NCT05425329
NCT05425329已完成不适用

Safety and Efficacy of a Probiotic Supplement: Focus on Lessening Gastrointestinal Distress in Endurance Athletes

University of Memphis2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2020年8月1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
17
试验地点
2
主要终点
Effect of probiotic supplementation on intestinal fatty acid binding protein (iFABP) levels.

研究概览

简要总结

Exercise-induced gastrointestinal dysfunction is common amongst endurance athletes and is characterized by gastrointestinal permeability, also known as "leaky gut." Probiotics have been shown to improve gut permeability through the secretion of mucin, immunoglobulin A and improvement in stability of tight junctions between epithelial cells. This study will determine the efficacy of a probiotic containing the bacterial strains P. acidilatici, CECT 7483, L. plantarum CECT 7484, L. plantarum CECT7485) in altering markers of gut inflammation and dysfunction, and symptoms of gastrointestinal distress.

详细描述

This study is a randomized, placebo-controlled, double-blinded crossover study where trained runners that experience moderate gastrointestinal discomfort with exhaustive runs will be subjected to the probiotic intervention/placebo supplementation for one month with a one month washout period. The intervention consists of the probiotic strains Lactobacillus plantarum (CECT7484 and CECT7485) and Pediococcus acidilactici (CECT7483) at a ratio of 1:1:1 at a dose of 3b cfu/day. Probiotic/Placebo capsules will be taken once daily. Biological samples and symptom data collection will be collected at baseline and after one month of probiotic/placebo supplementation. Data are also collected after an in-house treadmill run after one month of supplementation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Males, females between 18-50 years of age
  • Healthy and injury free as determined by screening questions and medical history
  • Distance runners as determined by physical activity questionnaire; run = 15 miles/week, run = 3 time or more/week
  • VO2max level of = 40ml/kg/min for males or = 35ml/kg/min for females
  • Agree to maintain normal diet and exercise routine throughout study
  • Agrees to collect stool samples as needed
  • Agree to complete questionnaires, records

排除标准

  • Women who are pregnant or breastfeeding, or plan to become pregnant during course of the study will not be included as the effect of probiotic on pregnancy and lactation is not established.
  • Subjects with a known allergy to the test material (active and placebo)
  • Subjects taking NSAIDs, Metformin, probiotics, or supplements that might alter the gut microbiome;these will be assessed individually. (Multivitamin and protein supplementation are allowed)
  • Subject that have abnormal test results during screening.
  • Alcohol or drug abuse within past year (alcohol can impair gut barrier).
  • History of GI surgery within past year as it would alter the gut microbiome (excluding appendectomy and herniorrhaphy).
  • Severe heart, liver, kidney, neurological, oncological or psychiatric disease, or immunosuppressed subjects will be excluded.
  • Coeliac disease, inflammatory bowel disease or acute pancreatitis (all 3 can impair gut barrier)
  • Regular use of antacid medication (can significantly alter microbiota)
  • Subject following a low FODMAP (fermentable oligo-, di-, mono-saccharides and polyols) diet will be excluded as this dietary pattern can alter the intestinal response to exercise in some people.

结局指标

主要结局

Effect of probiotic supplementation on intestinal fatty acid binding protein (iFABP) levels.

时间窗: 4 weeks

Determine concentration (pg/ml) of iFABP in serum

Effect of probiotic supplementation on lipopolysaccharide binding protein (LBP) levels

时间窗: 4 weeks

Determine concentration (ng/ml) of LBP in serum

Effect of probiotic supplementation on zonulin levels

时间窗: 4 weeks

Determine concentration (ng/ml) of zonulin in serum

Effect of probiotic supplementation on calprotectin levels

时间窗: 4 weeks

Determine concentration (ug/g) of calprotectin in feces.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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