NCT05037877已完成不适用
An Exploratory Investigation of Dietary Supplementation and Its Effect
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 110
- 试验地点
- 1
- 主要终点
- Quality of life improvements [Time Frame: Baseline to 8 weeks)
研究概览
简要总结
The primary objective of this study is to understand if the test product (HUM supplement) improve symptoms experienced.
详细描述
This will be a 2-arm randomized, double-blinded, placebo-controlled study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 38 Years 至 60 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Willing to maintain the current dietary pattern, activity level, and stable body weight for the duration of the study
- •Must be in good health (don't report any medical conditions asked in the screening questionnaire)
- •Willing and able to provide written informed consent
排除标准
- •Allergies to any test product ingredients
- •Any other severe chronic disease
- •Pregnant, want to become pregnant for the duration of the study, or who are breastfeeding
- •Participating in an investigational health product research study
研究组 & 干预措施
Placebo group
Placebo Comparator
Placebo supplement - 1 capsule per day
干预措施: Placebo (Dietary Supplement)
Intervention group
Active Comparator
HUM supplement - 1 capsule per day
干预措施: HUM supplement (Dietary Supplement)
结局指标
主要结局
Quality of life improvements [Time Frame: Baseline to 8 weeks)
时间窗: 8 week
Survey-based assessment (0-5 scale) with higher scores representing an improved outcome
次要结局
未报告次要终点
研究者
研究点 (1)
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