- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07395414
Effect of Different Work-to-rest Ratios During Simulated Taekwondo Combat on Blood Lactate, Heart Rate and Perceptual Responses in Elite Taekwondo Athletes
January 31, 2026 updated by: Bayram Ceylan, Kastamonu University
Randomized Cross-over Study
This randomized cross-over study measured physiological and perceptual responses of taekwondo athletes following a free combat and combats with different W:R ratios.
This study was carried out with 4 visits.
The first one included body composition measurements and familiarization to the sessions and measurements.
During the rest 3 visit, athletes performed simulated combats free and with 1:2 (10 sec work and 20 sec rest), and 2:1 (20 sec work and 10 sec rest) W:R ratios.
During all combat sessions, athletes heart rate (HR), blood lactate (bLA), and counter-movement jump performance (CMJ) were measured at rest and at the end of each combat.
HR was also measured following each set.
Athletes' rating of perceived exertion (RPE) and perceived muscle soreness (PMS) were measured immediately after each combat.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
20
Phase
- Not Applicable
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
-
-
-
Kastamonu, Turkey (Türkiye)
- Kastamonu University Faculty of Sport Sciences Physiology Lab
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- having at least brown belt,
- having at least 5 years of taekwondo experience,
- having no injuries for the last 6 months that prevent participating to trainings,
- competing at national championship and international tournaments during the last year
Exclusion Criteria:
- not having a brown belt,
- having less than 5 years of taekwondo experience,
- having injuries for the last 6 months that prevent participating to trainings,
- Not competing at national championship and international tournaments during the last year
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 Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Visit 1
|
Athletes completed a taekwondo combat for 3 sets of 2 minutes
|
|
Experimental: Visit 2
|
Athletes completed a taekwondo combat for 3 sets of 2 mins with 1:2 work to rest ratio (10 sec work and 20 sec rest)
|
|
Experimental: Visit 3
|
Athletes completed a taekwondo combat for 3 sets of 2 minutes with 2:1 work to rest ratio (20 second work and 10 second rest)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lactate
Time Frame: Immediately after each intervention
|
Athletes' lactate levels immediately after the exercise
|
Immediately after each intervention
|
|
Heart rate
Time Frame: Before and immediately after each intervention
|
Athletes' heart rate responses
|
Before and immediately after each intervention
|
|
CMJ
Time Frame: Before and immediately after each intervention
|
Athletes' CMJ was measured before and after each exercise session.
|
Before and immediately after each intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
RPE
Time Frame: Immediately after each intervention
|
Athletes' RPE was measured immediately after each exercise.
|
Immediately after each intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Bayram Ceylan, PhD, Kastamonu University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Bridge CA, Jones MA, and Drust B. Physiological responses and perceived exertion during international Taekwondo competition. International Journal of Sports Physiology And Performance 4: 485-493, 2009.
- Bouhlel E, Jouini A, Gmada N, Nefzi A, Ben Abdallah K, and Tabka Z. Heart rate and blood lactate responses during Taekwondo training and competition. Science & Sports 21: 285-290, 2006.
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)
March 5, 2023
Primary Completion (Actual)
April 15, 2023
Study Completion (Actual)
June 5, 2023
Study Registration Dates
First Submitted
January 24, 2026
First Submitted That Met QC Criteria
January 31, 2026
First Posted (Actual)
February 9, 2026
Study Record Updates
Last Update Posted (Actual)
February 9, 2026
Last Update Submitted That Met QC Criteria
January 31, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 2022-KAEK-12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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