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Vitamin D Intervention and Associated Changes in the Gut Microbiome and Vitamin D Levels in Healthy Adults (VDMT Trial)
N/A
Waitlist Available
Led By Kristen L Greathouse, PhD
Research Sponsored by Baylor University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Adult 18 years or older
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Summary
This trial will study the effect of vitamin D supplementation on the microbiome in healthy humans.
Eligible Conditions
- Colorectal Cancer
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Microbiome alterations
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Vitamin D interventionExperimental Treatment1 Intervention
A vitamin D gummie the same consistency and nutrient value as the placebo gummie will be taken as four gummies at the largest meal for 12 weeks once per day providing 4000 IUs per day or 1000 IUs per gummie
Group II: Placebo interventionPlacebo Group1 Intervention
A gummie candy the same consistency and nutrient value as the vitamin D gummie without any vitamin D will be taken as four gummies at the largest meal for 12 weeks once per day
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Who is running the clinical trial?
Baylor UniversityLead Sponsor
61 Previous Clinical Trials
65,909 Total Patients Enrolled
Kristen L Greathouse, PhDPrincipal InvestigatorBaylor University