A Clinical Study to Assess the Effect of a Supplement on Digestive Health, Overall Well-being, and Participant Experience.

Amway

Status

Completed

Conditions

Digestive System Disease

Treatments

Dietary Supplement: Greens powder

Study type

Interventional

Funder types

Industry

Identifiers

NCT06283732

20392

Details and patient eligibility

About

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.

Enrollment

70 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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) .