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Iron Absorption and Exercise

Fractional Iron Absorption in Response to an Acute Bout of Exercise

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04079322
Enrollment
31
Registered
2019-09-06
Start date
2019-08-22
Completion date
2019-12-04
Last updated
2020-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Iron-deficiency, Iron Deficiency Anemia

Brief summary

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.

Interventions

OTHERMeal

Participants will consume a meal containing a stable iron isotope following exercise or rest.

Sponsors

Florida State University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Members of the Florida State University Cross Country team * Refrain from using any pain-relievers (e.g., acetaminophen, nonsteroidal anti-inflammatory drugs such as aspirin, Advil®, Aleve®, Naprosyn®), or any other aspirin-containing product on the 2 study days * Refrain from using vitamin or mineral supplements on the study days

Exclusion criteria

* Musculoskeletal injury that compromise the ability to exercise

Design outcomes

Primary

MeasureTime frameDescription
Change in fractional iron absorptionRed blood cells collected on day 0 and day 14Stable iron isotopes

Secondary

MeasureTime frameDescription
Change in concentration of soluble transferrin receptor in nmol/LDay 0 and day 14Blood measure
Change in concentration of hemoglobin in g/LDay 0 and day 14Blood measure
Change in concentration of ferritin in ng/mLDay 0 and day 14Blood measure
Change in concentration of hepcidin in ng/mLDay 0 and day 14Blood measure
Change in concentration of IL-6 in pg/mLDay 0 and day 14Blood measure
Change in concentration of hematocrit as %Day 0 and day 14Blood measure

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026