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Effect of Iron-fortified Pea Powder on Exercise Performance

Effect of Low-phytate Pea Powder With High Iron Bioavailability on Iron Status of Female Runners

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04872140
Enrollment
28
Registered
2021-05-04
Start date
2021-05-03
Completion date
2022-08-15
Last updated
2022-10-13

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

Conditions

Iron-deficiency

Brief summary

Female endurance athletes are susceptible to iron deficiency and this can impact their exercise performance. This study assesses the impact of an pea protein supplement with high iron bio-availability on iron status and exercise performance.

Detailed description

Female endurance athletes are susceptible to iron deficiency due to poor iron intake from diets or possibly because of destruction of red blood cells during foot-strike hemolysis. This study will evaluate the impact of 8-weeks of iron supplementation through consumption of a pea-protein power that has high iron bio-availability due to low phytate levels. This will be compared to consumption of regular iron protein powder and maltodextrin placebo by randomizing participants to three groups. Participants will be assessed at baseline and after 8 weeks of supplementation for exercise performance (maximal aerobic capacity and a 5 km time trial running test), blood levels of ferritin and hemoglobin, and body composition (fat mass and lean tissue mass).

Interventions

DIETARY_SUPPLEMENTLow phytate pea powder

Exercise performance with low phytate pea powder

DIETARY_SUPPLEMENTRegular pea powder

Exercise performance with regular pea powder

DIETARY_SUPPLEMENTPlacebo (maltodextrin)

Exercise performance with placebo (maltodextrin)

Sponsors

University of Saskatchewan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

The powder supplements are being administered in a blinded manner. An individual who is separate from the rest of the research team will generate the allocation schedule and prepare the supplement packages so that participants, investigators, and outcome assessors are blinded. Statistical analysis will be blinded by coding of groups

Intervention model description

Participants are being randomized to three groups for the 8-week intervention: 1. Pea power with high iron bio-availability 2. Regular pea powder 3. Placebo (maltodextrin)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Female * Regularly participate in aerobic endurance training

Exclusion criteria

* Any contra-indications to exercise testing as determined with the Get Active Questionnaire

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in ferritin levelsUp to 8 weeksblood ferritin levels

Secondary

MeasureTime frameDescription
Change from baseline in hemoglobin levelsUp to 8 weeksBlood hemoglobin concentration
Change from baseline in maximal aerobic capacityUp to 8 weeksMaximal aerobic capacity (mL/kg/min) measured on a treadmill
Change from baseline in exercise time trial performanceUp to 8 weeksTime (minutes) to complete 5 km running on a treadmill
Change from baseline in lean tissue massUp to 8 weeksLean tissue mass (kg) measured with dual energy X-ray absorptiometry
Change from baseline in fat massUp to 8 weeksFat mass (kg) measured with dual energy X-ray absorptiometry

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026