- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01100905
An Iron-containing Food Product for the Prevention of Diminished Iron Status in Soldiers
April 23, 2010 updated by: United States Army Research Institute of Environmental Medicine
Utility of an Iron-containing Food Product for the Prevention of Diminished Iron Status During Basic Combat Training
Military personnel face intense physical and cognitive demands.
Diminished iron status affects physiologic responses to these challenges.
Both cross-sectional and longitudinal studies indicate a significant decrement in iron status in enlisted female military personnel immediately following basic combat training (BCT).
Decrements in iron status are associated with diminished cognitive and physical performance, and may affect body composition.
The primary objective of this randomized, placebo controlled study is to assess the utility of an iron-containing food product for maintaining iron status during BCT.
This study will provide insight into the utility and efficacy of an iron-containing food product for the maintenance of iron status during military training.
Furthermore, it will provide novel scientific data regarding the relationship between iron status and physical and cognitive performance in female Soldiers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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South Carolina
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Columbia, South Carolina, United States, 29207
- Fort Jackson
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 42 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Female US Army Recruit
- Participating in Basic Combat Training
Exclusion Criteria:
- Male
- Pregnancy
- Diagnosed hemochromatosis
- Diagnosed thalassemia
- History of ulcerative colitis
- Allergy to chocolate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
April 7, 2010
First Submitted That Met QC Criteria
April 8, 2010
First Posted (Estimate)
April 9, 2010
Study Record Updates
Last Update Posted (Estimate)
April 26, 2010
Last Update Submitted That Met QC Criteria
April 23, 2010
Last Verified
April 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H08-11
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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