Vitamin D for Improving Metabolic Control and Depressive Symptoms
NCT ID: NCT01185574
Last Updated: 2013-07-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2009-10-31
2012-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Vitamin D supplementation
The study medication (a capsule of 50,000 IU of vitamin D2) will be administered once a week for six months.
Vitamin D supplementation
Vitamin D2 50,000 IU will be administered once a week for six months.
Interventions
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Vitamin D supplementation
Vitamin D2 50,000 IU will be administered once a week for six months.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. medically stable type 2 diabetes with HBA1c \<9%.
3. significantly elevated depressive symptoms as measured by a score greater than or equal to 14 using the Center for Epidemiologic Studies Depression Tool (CES-D.
Exclusion Criteria
2. malabsorption problems (e.g., crohn's disease, celiac sprue)
3. hypercalcemia-level greater than 10.5 mg/dl
4. Severe complications of diabetes (amputation, blindness, or renal problems) 5) Women with low thyroid function
18 Years
FEMALE
No
Sponsors
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Loyola University
OTHER
Responsible Party
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Sue Penckofer
Professor
Locations
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Loyola University Medical Center
Maywood, Illinois, United States
Countries
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Other Identifiers
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201255
Identifier Type: -
Identifier Source: org_study_id
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