A Clinical Study to Assess the Effect of a Supplement on Digestive Health, Overall Well-being, and Participant Experience.
Not Applicable
Completed
- Conditions
- Digestive System Disease
- Interventions
- Dietary Supplement: Greens powder
- Registration Number
- NCT06283732
- Lead Sponsor
- Amway Corp
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
- 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 .
Exclusion Criteria
- 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) .
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Dietary Supplement: Greens powder Greens powder Participants are to consume one scoop (8.5 g) of the greens powder mixed in 8-10 oz of water every morning before breakfast for two weeks.
- Primary Outcome Measures
Name Time Method Digestive Health Improvement 14 days from the start of intervention Measure the change in digestive health using daily diaries and the Bristol Stool Scale (BSS).
- Secondary Outcome Measures
Name Time Method Quality of Life and Well-being Enhancement 14 days from the start of intervention Assess improvements in participants' quality of life, energy levels, satiety, and overall well-being through validated questionnaires.
Trial Locations
- Locations (1)
Citruslabs
🇺🇸Santa Monica, California, United States