- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03677674
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
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.
Sponsor
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
Additional Relevant MeSH Terms
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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