The Effects of Dehydration on the Performance of Judoka

September 18, 2018 updated by: Laurent Chapelle, Vrije Universiteit Brussel
Dehydration is a common phenomenon in judo that can lead to negative performance such as a decline in strength, a decline in anaerobic performance, a reduced body fluid balance, glycogen depletion and worsened psychological parameters. Therefore, we want to simulate several judo combats and look at the performances whether they change during a competition day. We also want to see if the results are different in a dehydrated versus euhydrated state.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

27

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

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • judoka
  • minimum 18 years
  • men and women
  • only dehydration: sauna, warm bath, sweat suit

Exclusion Criteria:

  • injured
  • sick
  • not underaged (18 years)

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: OTHER
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: dehydrated
The participants will be dehydrated (at least 2% of their body weight) before performing the Sterkowicz test.
Participants will be dehydrated (2% of their body weight) using sauna.
NO_INTERVENTION: euhydrated
The participants will be normally hydrated (= euhydration) before performing the Sterkowicz test (i.e. no specific intervention will be implemented).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sterkowicz test
Time Frame: Up to 3 weeks
Sterkowicz test
Up to 3 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
heart rate
Time Frame: Up to 3 weeks
Heart rate will be determined using the Polar H1 (Polar, Kempele, Finland)
Up to 3 weeks
Body weight
Time Frame: Up to 3 weeks
Body weight will be assessed to the nearest 0.002 kg using the WLT 60/120/X/L3 scale (All Scales Europe, Veen, The Netherlands)
Up to 3 weeks
Borg Rating of Perceived Exertion Scale
Time Frame: Up to 3 weeks
The Borg Rating of Perceived Exertion scale is a numerical scale (to determine exertion) that ranges from 6 to 20, where 6 means "no exertion at all" and 20 means "maximal exertion.
Up to 3 weeks
body temperature
Time Frame: Up to 3 weeks
Body temperature will be determined using the Adtemp 421 Digital Ear Thermometer (American Diagnostics Corporations, Hauppauge, New York, United States of America)
Up to 3 weeks

Collaborators and Investigators

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

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 (ANTICIPATED)

October 1, 2018

Primary Completion (ANTICIPATED)

December 20, 2019

Study Completion (ANTICIPATED)

January 30, 2020

Study Registration Dates

First Submitted

July 24, 2018

First Submitted That Met QC Criteria

September 18, 2018

First Posted (ACTUAL)

September 19, 2018

Study Record Updates

Last Update Posted (ACTUAL)

September 19, 2018

Last Update Submitted That Met QC Criteria

September 18, 2018

Last Verified

September 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • VrijeUniversiteitB

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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