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Vitamin D in milk

  • Status
    Accepting Candidates
  • Age
    18 Years - N/A
  • Sexes
    All
  • Healthy Volunteers
    No
I'm interested
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Objective

The overall goal is to enhance vitamin D status in a safe and effective manner. A 3-week randomized comparator-controlled trial among a cohort of adults with CKD (stages 3-5) (n=24)

Will test the main objective: Evaluate the bioefficacy of D3 in micro and nanoparticles (4000IUs) in almond milk with the sub-objective of: Explore the effect of D3 in micro and nanoparticles (4000IUs) in almond milk on inflammation markers CRP, TNF-α and IL-6.

Details

Full study title Almond milk with vitamin D: The impact on vitamin D status
Protocol number OCR41655
ClinicalTrials.gov ID NCT05165173
Phase N/A

Eligibility

Inclusion Criteria:

  • adults who have been diagnosed with CKD

  • have no GI disorders or GI disturbances

  • age 18 years or older

  • no food allergies or dietary restrictions

  • all with no contraindications to consuming anything by mouth as per their physician

Exclusion Criteria:

  • no diagnosis of CKD

  • GI disorders

  • gastrointestinal disturbances

  • under 18 years old

  • food allergies to almonds

  • Dietary restrictions as medically indicated

  • trouble chewing/swallowing as confirmed by physician

Participate in a study

Here are some general steps to consider when participating in a research study:

  1. Step
    1

    Contact the research team

    Call or email the research team listed within the specific clinical trial or study to let them know that you're interested. A member of the research team, such as the researcher or study coordinator, will be available to tell you more about the study and to answer any questions or concerns you may have.

    Primary contact

    Jeanette Andrade
  2. Step
    2

    Get screened to confirm eligibility

    You may be asked to take part in prescreening to make sure you are eligible for a study. The prescreening process ensures it is safe for you to participate. During the prescreening process, you will be asked some questions and you may also be asked to schedule tests or procedures to confirm your eligibility.

  3. Step
    3

    Provide your consent to participate

    If you are eligible and want to join the clinical trial or study, a member of the research team will ask for your consent to participate. To give consent, you will be asked to read and sign a consent form for the study. This consent form explains the study's purpose, procedures, risks, benefits and provides other important information, such as the study team's contact information.

  4. Step
    4

    Participate

    If you decide to participate in a clinical trial or study, the research team will keep you informed of the study requirements and what you will need to do to throughout the study. For some trials or studies, your health care provider may work with the research team to ensure there are no conflicts with other medications or treatments.