NCT06283732已完成不适用
A Clinical Study to Assess the Effect of a Supplement on Digestive Health, Overall Well-being, and Participant Experience.
Amway Corp2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年11月15日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 70
- 试验地点
- 2
- 主要终点
- Digestive Health Improvement
研究概览
简要总结
The study aims to evaluate the effectiveness of a dietary supplement (greens powder), on improving digestive health, quality of life, energy levels, and satiety over a 14-day period. Participants, aged 18-65 and experiencing mild digestive issues, will consume the greens powder daily and report outcomes through diaries and questionnaires.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female.
- •Aged 18-65 years.
- •Willing to comply with study requirements.
- •No known allergies to the ingredients listed in the product.
- •Self-reported mild digestive issues (e.g., occasional bloating, stomach discomfort, occasional constipation, or occasional diarrhea).
- •Generally healthy - do not live with any uncontrolled chronic disease .
排除标准
- •Pre-existing chronic conditions that would prevent adherence to the protocol, including oncological and psychiatric disorders.
- •Known severe allergic reactions that require an Epi-Pen.
- •Women who are pregnant, breastfeeding, or attempting to conceive.
- •History of severe diagnosed digestive disorders (e.g., IBS, IBD, Crohn's disease) or gastrointestinal-tract surgeries.
- •Unwillingness to follow the study protocol.
- •Invasive medical procedure within the last three weeks or planning one during the study period.
- •History of substance abuse.
- •Current participation or planning to participate in another research study.
- •Regular consumption of probiotics, fiber, or prebiotic supplements within 3 weeks of the study.
- •Regular intake of medications that may interfere with the study or study product (e.g., anticoagulants, laxatives, sedatives, beta-blockers, anti-acids) .
结局指标
主要结局
Digestive Health Improvement
时间窗: 14 days from the start of intervention
Measure the change in digestive health using daily diaries and the Bristol Stool Scale (BSS).
次要结局
- Quality of Life and Well-being Enhancement(14 days from the start of intervention)
研究者
研究点 (2)
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