NCT05037877
Completed
Not Applicable
An Exploratory Investigation of Dietary Supplementation and Its Effect
ConditionsQuality of Life
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Quality of Life
- Sponsor
- HUM Nutrition, Inc.
- Enrollment
- 110
- Locations
- 1
- Primary Endpoint
- Quality of life improvements [Time Frame: Baseline to 8 weeks)
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
The primary objective of this study is to understand if the test product (HUM supplement) improve symptoms experienced.
Detailed Description
This will be a 2-arm randomized, double-blinded, placebo-controlled study.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Quality of life improvements [Time Frame: Baseline to 8 weeks)
Time Frame: 8 week
Survey-based assessment (0-5 scale) with higher scores representing an improved outcome
Study Sites (1)
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