Dietary Assessment
Conditions
Keywords
Dietary Supplement, Healthy Adults
Brief summary
Healthy Adult subjects
Detailed description
The study will be a prospective randomized, controlled clinical study. There will be interventional treatment for a total of 12 weeks. The subjects will attend two appointments in the clinic throughout the duration of the study.
Interventions
DIETARY_SUPPLEMENTREDS Powder
Dietary supplement powder
Sponsors
Prenetics Global
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* BMI between 18.5 and 30 kg/m2 * Low, moderate, and high activity (self-identified) \* * Self-identify as having fatigue, and abdominal issues (bloating, constipation etc.) \* * Participants will be able to read, understand and sign an informed consent form (includes HIPAA and States requirements) and sign a photo release form. * Participants are willing and able to follow all study directions, attend study visits as scheduled and must be willing to accept the restrictions of the study including but not limited to: * Willing to refrain from introducing any new diets or dietary supplements for the duration of the study
Exclusion criteria
\-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Body Morphology | 12 weeks | Subjects assessed through weight and height which will be combined to determine BMI and abdominal and thigh circumference and images before and after |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Safety and Tolerability | 12 weeks | Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 |
| Energy | 12 weeks | Assessed by subjective questionnaire |
| Changes in Micronutrient blood levels | 12 weeks | Assessed through laboratory assays of vitamins and minerals in the blood |
Countries
United States
Outcome results
None listed