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Observational Study to Evaluate Changes in Iron, Vit-D, and CRP During a Twelve to Twenty-Four Week Supervised Triathlon Training Program

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City:   Sioux Falls
State:   South Dakota
Zip Code:   57105
Conditions:   Anemia - Vitamin D Deficiency
Purpose:   The purpose of this study is to observe changes in iron status and vitamin D status during a 12-24 week supervised training program, specifically males and females between the ages of 30 and 50 years old.
Study Summary:   Study subjects will be participants in a triathlon training program through the Avera Sports Institute in Sioux Falls, SD. This clinical study will examine changes in iron and vitamin D levels. Blood specimens will be collected at baseline and again after 3 and 6 months of participating in the training program.
Criteria:   Inclusion Criteria: - Males and premenopausal females between the ages of 30 and 50 years old - Training through the Avera Sports Institute Triathlon Training Program - Agree to keep diet, exercise and all current health habits stable during participation in the study Exclusion Criteria: - Women who are pregnant, breastfeeding or planning to become pregnant - Has a chronic disease that affects calcium or bone metabolism - Has a chronic disease that affects iron metabolism or iron storage - Has kidney disease - Has any laboratory or biometric value that would indicate an issue for the safety of the study subject - Is currently participating in another clinical research study
NCT ID:   NCT01328704
Primary Contact:   Principal Investigator
Matthew Vukovich, PhD
South Dakota State University

Sarah VanLaecken, EP, MA
Phone: 605-322-3278
Email: sarah.vanlaecken@avera.org
Backup Contact:   Email: mike.jahnke@avera.org
Mike Jahnke
Phone: 605-322-3067
Location Contact:   Sioux Falls, South Dakota 57105
United States

Sarah VanLaecken, EP, MA
Phone: 605-322-3278
Email: sarah.vanlaecken@avera.org

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 23, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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