Iron Metabolism in Dragon Boat Athletes

July 21, 2012 updated by: Andree Hillebrecht, University of Giessen

Iron Metabolism in Dragon Boat Athletes - An Analysis of Changes in Blood Count Parameters Under Sport-specific Stress

The purpose of the study is:

  • To investigate the effect of sport-specific stress in the iron metabolism of dragon boat athletes
  • To investigate the effects of sport-specific stress in the activity of pro-hepcidin and hepcidin

Study Overview

Detailed Description

This investigation evaluates the effects of sport-specific stress in iron metabolism of dragon boat athletes. Recent studies showed a significant increase in hepcidin activity under exercise (Röcker L. et al.(2005): Iron regulatory protein hepcidin is increased in female athletes after a marathon. European Journal of Applied Physiology, S. 95, 569-571)which possibly influences the iron metabolism.

In particular in this investigation the activity of pro-hepcidin and hepcidin under sport-specific stress is analysed. Therefore elite dragonboat athletes will be included to this study. Every athlete is tested once. At one exercise day from every athlete the iron metabolism especially the change of hepcidin, prohepcidin and iron before and after a specific dragonboat intervention is analysed.

Study Type

Interventional

Enrollment (Anticipated)

40

Phase

  • Not Applicable

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • athletes performing dragon boat sport

Exclusion Criteria:

  • acute clinically significant intercurrent diseases

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

  • Primary Purpose: Diagnostic
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: sports intervention male
male athletes of the german national dragon boat team
male athletes of the german national dragon boat team performing three specific training units at one day
Active Comparator: sports intervention women
women athletes of the german national dragon boat team
women athletes of the german national dragon boat team performing two specific training units and one weight lifting test at one day

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change from Baseline in prohepcidin after performing dragonboating
Time Frame: pre and post exercise intervention at the same day
one meassurement of prohepcidin immediate before and within three hours after performing two to four specific dragonboat interventions at the same day
pre and post exercise intervention at the same day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
haematocrit
Time Frame: pre and post exercise intervention at the same day
one meassurement of haematocrit immediate before and within three hours after performing two to four specific dragonboat intervention at the same day
pre and post exercise intervention at the same day
value of reticulocytes
Time Frame: pre exercise
one meassurement of reticulocytes immediate before performing two to four specific dragonboat interventions
pre exercise
value of hypochromic erythrocytes
Time Frame: pre exercise
one meassurement of hypochromic erythrocytes immediate before performing two to four specific dragonboat interventions
pre exercise
change from Baseline in serum iron after performing dragonboating
Time Frame: pre and post exercise intervention at the same day
one meassurement of serum iron immediate before and within three hours after performing two to four specific dragonboat interventions at the same day
pre and post exercise intervention at the same day
value of transferrin
Time Frame: pre exercise
one meassurement of transferrin immediate before performing two to four specific dragonboat interventions
pre exercise
value of transferrin saturation
Time Frame: pre exercise
one meassurement of transferrin saturation immediate before performing two to four specific dragonboat interventions
pre exercise
value of ferritin
Time Frame: pre exercise
one meassurement of ferritin immediate before performing two to four specific dragonboat interventions
pre exercise
change from Baseline in hepcidin after performing dragonboating
Time Frame: pre and post exercise intervention at the same day
one meassurement of hepcidin immediate before and within three hours after performing two to four specific dragonboat interventions at the same day
pre and post exercise intervention at the same day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Andree Hillebrecht, Dr. med., Department of sportsmedicine- University Giessen

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

April 1, 2011

Primary Completion (Actual)

April 1, 2012

Study Completion (Actual)

April 1, 2012

Study Registration Dates

First Submitted

August 31, 2011

First Submitted That Met QC Criteria

September 7, 2011

First Posted (Estimate)

September 9, 2011

Study Record Updates

Last Update Posted (Estimate)

July 24, 2012

Last Update Submitted That Met QC Criteria

July 21, 2012

Last Verified

July 1, 2012

More Information

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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