- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05707455
Hematological Factors and Iron Status in Aerobic Versus Anaerobic Training in Athletic Females
September 24, 2023 updated by: Doaa A. Osman, Cairo University
Hematological Factors and Iron Status in Aerobic Versus Anaerobic Training in Athletic Females: An Observational Study
This study aimed to evaluate the hematological factors and iron status in aerobic versus anaerobic training in athletic females.
Study Overview
Status
Completed
Conditions
Detailed Description
In both the short and long term, physical training causes iron status deterioration in sporty females.
Nonetheless, little is known about the effect of different forms of exercise (aerobic versus anaerobic) on haematological variables and iron status in sporty females during adolescence.
As a result, the purpose of this study was to compare the haematological variables and iron status in aerobic versus anaerobic exercise in adolescent female athletes.
Another goal was to compare aerobic and anaerobic groups in terms of iron status classifications, such as normal iron status, iron deficiency with or without anaemia.
Study Type
Observational
Enrollment (Actual)
25
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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Cairo, Egypt
- Local clubs
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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
16 years to 19 years (Child, Adult)
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
They were chosen via advertisement in local Cairo clubs.
Description
Inclusion Criteria:
- Healthy, virginal, nonsmoker, female athletes.
- Age from 16 to 19 years.
- Body mass index < 25 kg/m2.
- Having the same socio-economic level.
- Following a normal balanced nutrition.
Exclusion Criteria:
- Using any medical or hormonal therapy that might influence the iron status.
- Vegetarian athletes.
- Having menorrhagia or amenorrhea.
- Chronic inflammatory condition or existing infection.
- Diabetic, hypertensive or cardiac athletes.
- Haematological disease (with the exception of iron deficiency with or without anaemia).
- Having transfusion of blood.
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?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Aerobic group
long distance runners
|
evaluating blood levels of hemoglobin, hematocrit, red blood cell count, mean corpuscular volume, mean corpuscular hemoglobin concentration, serum transferrin and serum ferritin.
|
Anaerobic group
broad jumpers
|
evaluating blood levels of hemoglobin, hematocrit, red blood cell count, mean corpuscular volume, mean corpuscular hemoglobin concentration, serum transferrin and serum ferritin.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment of hemoglobin (Hb)
Time Frame: 2 months
|
Blood samples were collected between 8:00 and 9:00 a.m. after an overnight fast and time of relaxation.
The athletic girls were asked to refrain from exercising the day before sample.
Blood was taken from the antecubital vein and placed in one EDTA tube and one beads tube for serum separation.
An automatic cell counter (Sysmex XS 1000, Japan) was used to measure hemoglobin (Hb).
|
2 months
|
Assessment of hematocrit (Hct)
Time Frame: 2 months
|
Blood samples were collected between 8:00 and 9:00 a.m. after an overnight fast and time of relaxation.
The athletic girls were asked to refrain from exercising the day before sample.
Blood was taken from the antecubital vein and placed in one EDTA tube and one beads tube for serum separation.
An automatic cell counter (Sysmex XS 1000, Japan) was used to measure hematocrit (Hct).
|
2 months
|
Assessment of red blood cell (RBC) count
Time Frame: 2 months
|
Blood samples were collected between 8:00 and 9:00 a.m. after an overnight fast and time of relaxation.
The athletic girls were asked to refrain from exercising the day before sample.
Blood was taken from the antecubital vein and placed in one EDTA tube and one beads tube for serum separation.
An automatic cell counter (Sysmex XS 1000, Japan) was used to measure red blood cell (RBC) count.
|
2 months
|
Assessment of mean corpuscular volume (MCV)
Time Frame: 2 months
|
Blood samples were collected between 8:00 and 9:00 a.m. after an overnight fast and time of relaxation.
The athletic girls were asked to refrain from exercising the day before sample.
Blood was taken from the antecubital vein and placed in one EDTA tube and one beads tube for serum separation.
An automatic cell counter (Sysmex XS 1000, Japan) was used to measure mean corpuscular volume (MCV).
|
2 months
|
Assessment of mean corpuscular hemoglobin concentration (MCHC)
Time Frame: 2 months
|
Blood samples were collected between 8:00 and 9:00 a.m. after an overnight fast and time of relaxation.
The athletic girls were asked to refrain from exercising the day before sample.
Blood was taken from the antecubital vein and placed in one EDTA tube and one beads tube for serum separation.
An automatic cell counter (Sysmex XS 1000, Japan) was used to measure mean corpuscular hemoglobin concentration (MCHC).
|
2 months
|
Assessment of serum transferrin
Time Frame: 2 months
|
Blood samples were collected between 8:00 and 9:00 a.m. after an overnight fast and time of relaxation.
The athletic girls were asked to refrain from exercising the day before sample.
Blood was taken from the antecubital vein and placed in one EDTA tube and one beads tube for serum separation.
The serum sample was centrifuged, and the serum transferrin was measured using COBAS Integra 400 plus, Switzerland.
|
2 months
|
Assessment of serum ferritin
Time Frame: 2 months
|
Blood samples were collected between 8:00 and 9:00 a.m. after an overnight fast and time of relaxation.
The athletic girls were asked to refrain from exercising the day before sample.
Blood was taken from the antecubital vein and placed in one EDTA tube and one beads tube for serum separation.
The serum sample was centrifuged, and the serum ferritin was measured using ADVIA Centaur XPT, Germany.
|
2 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Anthropometric measures
Time Frame: 2 months
|
A weight-height scale was used to assess the weight (Kg) and height (m) for each female athlete in the two groups.
The body mass index (BMI) was then calculated by dividing the weight by the height squared (Kg/m2).
|
2 months
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Assessment of participation age to sport
Time Frame: 2 months
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Each female athlete was asked about her age of participation to sport to assess her training profile.
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2 months
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Assessment of number of hours of training per week
Time Frame: 2 months
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Each female athlete was asked about the number of hours of training per week to assess her training profile.
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2 months
|
Assessment of training experience
Time Frame: 2 months
|
The training experience in years was calculated by subtracting the female athlete's age of participation to training from her chronological age.
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Doaa A Osman, Assis. Prof., Physical Therapy for Woman's Health, Faculty of physical therapy, Cairo University, Giza, Egypt.
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 Major Dates
Study Start (Actual)
September 1, 2022
Primary Completion (Actual)
October 31, 2022
Study Completion (Actual)
October 31, 2022
Study Registration Dates
First Submitted
January 20, 2023
First Submitted That Met QC Criteria
January 28, 2023
First Posted (Actual)
February 1, 2023
Study Record Updates
Last Update Posted (Actual)
September 26, 2023
Last Update Submitted That Met QC Criteria
September 24, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004727
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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