Florida State University
Tallahassee, Florida, 32306, United States
NCT Number: NCT04079322
Iron is a nutritionally essential mineral required for optimal physical and cognitive performance. Endurance exercise often leads to declines in iron status; however, the reason for the decline is not known. The primary objective of the proposed study is to determine the effects of an acute bout of strenuous endurance exercise on iron absorption and status and markers of inflammation in human volunteers. The investigators hypothesize that an acute bout of strenuous endurance exercise, compared to rest, will reduce iron absorption, resulting in diminished iron status, and that reduced iron absorption will be negatively associated with markers of inflammation. A secondary objective is to monitor iron status throughout a season of competition.
Looking for future studies?
Notify MeAll sexes
Interventional
Not applicable
Tallahassee, Florida, 32306, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will consume a meal containing a stable iron isotope following exercise or rest.
Time frame: Red blood cells collected on day 0 and day 14
Stable iron isotopes
Time frame: Day 0 and day 14
Blood measure
Time frame: Day 0 and day 14
Blood measure
Time frame: Day 0 and day 14
Blood measure
Time frame: Day 0 and day 14
Blood measure
Time frame: Day 0 and day 14
Blood measure
Time frame: Day 0 and day 14
Blood measure
Florida State University
Other
Fractional Iron Absorption in Response to an Acute Bout of Exercise
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04744181
Anemia, Anemia, Hypochromic
Roma, Italy
View Trial DetailsNCT03897673
Anemia, Anemia in Children
Kampala, Uganda
View Trial DetailsNCT04705662
Anemia, Anemia, Hypochromic
Cambridge, Greater Manchester, United Kingdom
View Trial DetailsNCT04793906
Anemia, Anemia, Hypochromic
Baton Rouge, Louisiana, United States
View Trial Details