Development of a Marker of Adherence for Tracking Consumption of Nutrient Supplements
Completed · Not applicable
Conditions studied: Adherence, Treatment
In brief
The purpose of this study is to determine whether selected adherence markers can be used to track daily or intermittent consumption of nutrient supplements.
Key facts
- Study ID
- NCT04040543
- Run by
- University of California, Davis
- People needed
- 50
- Starts
- 2019-07-26
- Expected to finish
- 2020-11-30
- Last updated by the study team
- 2021-01-08
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- non-pregnant, non-lactating women
You may not qualify if…
- BMI <18.5kg/m2 or >25.0 kg/m2
- Diagnosis of chronic disease
- Use of medication that can affect gastrointestinal mobility
- Consumption of more than 7 alcoholic drinks per week
- Smoking
- Unwillingness to refrain from consuming dietary sources of the marker compound(s) 3 days prior to, and during the 12 day urine collection period
- Unwillingness to adhere to the study protocol
- Peanut allergy
- Cow milk allergy
- Soy allergy
- Almond allergy
- Allergy to adherence markers
- Pregnancy
Where it is running
- University of California, Davis — Davis, California, United States
Full record on ClinicalTrials.gov
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