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临床试验/NCT05560048
NCT05560048进行中(未招募)不适用

Anti-exercise-fatigue Effects of Rice Protein RP-80NY in Men

Chung Shan Medical University2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2022年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
18
试验地点
2
主要终点
Change the exercise performance after intervention compare the exercise

研究概览

简要总结

The aim of this study is to investigate the anti-exercise-fatigue effects of rice protein RP-80NY in men

详细描述

Each subject must undergo a maximum oxygen consumption test 1 week before the intervention (day 1), eat the test food for 28 days (day 1 to day 28), following 14 days of wash-out (day 29 to day 42), and undergo second maximum oxygen consumption test (day 43) and another test food intervention (day 43 to day 70). The assays of anthropometric measurement, diet questionnaire survey, grip strength test and fecal collection were carried out before and after the intervention (the 1st ,28th ,43th and 35th day). Each subject has to join the Wingate anaerobic test (day 21 and day 63), and the endurance exercise test (day 28 and day 70) during the intervention. All of the trial period was 70 days, and the blood samples of the subject will be collected at the times of exercise beginning, 15 min after exercise, the end of exercise, 1 hour after rest, 2 hour after rest ,and 3 hour after rest. During the whole period of participating in the program, blood will be collected 14 times, the blood volume of each times is 10 mL. Gas is collected before the period and within 1 hour, 2 hour and 3 hour after exercise (5 minute at a time). After intervention, the exercise time, oxygen intake, blood biochemical value and gut microbiota will be analyzed.

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
Single (Participant)

入排标准

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

入选标准

  • The subject is a male and aged 20-
  • The subject has a usual exercise habit (exercising 2 times or more per week) and did not participate in professional sports competitions or professional sports training during the study period.
  • No smoking or drinking habits.
  • No food allergies and the liver function is normal.
  • No cardiovascular diseases or other chronic diseases, and no serious illnesses requiring hospitalization during the study period.
  • The subject can understand the test process described in the consent form and the possible potential risks and benefits, and can sign the consent form.
  • The subject can accept dietary control during the trial period.

排除标准

  • Those who have taken nutritional supplements containing branched-chain amino acids.
  • Those who cannot complete the wingate anaerobic test and the endurance exercise test.
  • Those who are diagnosed with kidney disease, heart disease, or cancer and are still under active treatment.
  • Have used other drugs, whose pharmacological effects may affect fatigue.
  • Subjects who have systemic infections and require systemic antibiotics.

结局指标

主要结局

Change the exercise performance after intervention compare the exercise

时间窗: 21th day, 63th day

Duration of exhaustive exercise test (second) between pre- and post-intervention

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chin-Lin Hsu

Professor

Chung Shan Medical University

研究点 (2)

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