Evaluate the Change in Iron, Vitamin D, and C-Reactive Protein Level (CRP) in a 12 to 24 Week Period
Status: | Completed |
---|---|
Conditions: | Other Indications, Anemia, Gastrointestinal |
Therapuetic Areas: | Gastroenterology, Hematology, Other |
Healthy: | No |
Age Range: | 30 - 50 |
Updated: | 5/5/2014 |
Start Date: | January 2012 |
End Date: | October 2014 |
Contact: | Sarah VanLaecken, EP, MA |
Email: | sarah.vanlaecken@avera.org |
Phone: | 605-322-3278 |
Observational Study to Evaluate Changes in Iron, Vit-D, and CRP During a Twelve to Twenty-Four Week Supervised Triathlon Training Program
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.
12-24 week supervised training program, specifically males and females between the ages of
30 and 50 years old.
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.
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.
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
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