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临床试验/JPRN-UMIN000051307
JPRN-UMIN000051307已完成Unknown

Study to confirm the anti-stress effect of continuous ingestion of foods containing Lactobacillus brevis subsp. coagulans (Labre). - Study to confirm the anti-stress effect of continuous ingestion of foods containing Lactobacillus brevis subsp. coagulans (Labre).

Medical Corporation Hokubukai Utsukushigaoka Hospital0 个研究点目标入组 50 人开始时间: 2023年6月9日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) Subjects who have a history of heart, liver, kidney disease, organ damage, diabetes, or other serious diseases (2) Subjects who have a history of gastrointestinal surgery (excluding appendectomy) (3) Subjects who are currently receiving medical drug treatment (4) Subjects who are pregnant, wish to become pregnant during the study, or are breastfeeding (5) Subjects with intention to improve fatigue, stress or sleep who receive any treatments (including hospital visits or medical treatment) or who use any pharmaceuticals or health foods. (6) Subjects who have been diagnosed with chronic fatigue syndrome (7) Subjects who are under psychiatric consultation or have history of psychiatric consultation for mental disorders (depression, etc.) or sleep disorders (8) Subject who take beverage containing large amount of caffeine (400 mg/day or more) in daily base (9) Subjects who take foods or supplements containing lactobacilli or bifidobacteria 3 times or more a week (Suguki pickle, bran pickle, kimchi, "Labre capsules", etc.) (10) Shift workers including late-night shifts, or subjects who have extremely irregular eating, sleeping, or other lifestyle habits (11) Subjects who drink more than 60 g pure alcohol equivalent/day on average (12) Smokers (13) Subjects who are expected to undergo a major change in family or work environment or other stressful situation (e.g., job change, moving, marriage) from one month prior to the screening test to the end of this study. (14) Subjects who exercise heavily in daily base (15) Subjects who donated blood within 3 months at screening (16) Subjects who are participating in clinical research or monitoring (food, pharmaceuticals, cosmetics) other than this research, or plan to participate during this research period (17) Subjects who are judged to be inappropriate for this study with other reasons by the principal investigator.

研究者

发起方
Medical Corporation Hokubukai Utsukushigaoka Hospital

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