Effect of 8-week Incremental Elastic-Resistance Kick Training in Taekwondo Athlete's

August 22, 2024 updated by: Bruno Figueira

Effect of 8-week Incremental Elastic-Resistance Kick Training in Taekwondo Athlete's: Roundhouse Kick Quality and Physical Performance Analysis

This study aimed to assess the effects of an 8-week incremental elastic-resistance kick training program on the roundhouse kick quality and physical performance, in comparison to conventional training methods of youth Taekwondo athletes. A two-group parallel, randomized, quasi-experimental design was used, dividing Participants into experimental (n=11, age: 15.5 ± 1.5 years, stature: 169.5 ± 15.5 cm, body mass: 63.2 ± 26.2 kg; training experience: 7.0 ± 3.0 y) and control group (n=10, age: 14.8 ± 1.2 years, stature: 162.0 ± 14.0 cm, body mass: 53.15 ± 21.4 kg; training experience: 5.5 ± 1.5 y), undergoing tailored Elastic Resistance training alongside their regular Taekwondo regimen. The study measured various performance metrics including Roundhouse Kick velocity, impact scoring, isometric muscle strength, counter movement jump performance, and simple reaction times.

Study Overview

Study Type

Interventional

Enrollment (Actual)

37

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

      • Kaunas, Lithuania, 5555
        • Bruno Figueira

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Being part of a unified youth development program;
  • Minimum of four weekly training sessions, each session lasting 90 minutes.

Exclusion Criteria:

  • Musculoskeletal, neurological, or orthopedic injury that may impair their participation.

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: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental
In the experimental group, participants performed the RHK exercises using incrementally resistive elastic tubing. The RHKs targeted shields (Adidas, Curved Kick Shield) held at chest height. Each athlete started with a 2.4 m elastic tubing, one end attached to the ankle and the other to a stable platform, ensuring the tubing's resistance reached 50 N at full kicked extension (Fig.1). After four weeks (12 sessions), resistance increased to 100 N by adding another tubing. Each session comprised three sets of 6 RHKs per leg, at maximum speed, with 30-second intervals between kicks and 3-minute rests between sets. This 8-week, three times weekly, training regimen involved incremental ER training.
Athletes used tailored Elastic Resistance training
Other: Control
The control group undertook a similar RHK training regime in sequence and duration, mirroring the number of kicks performed by the experimental group, but without ER equipment. After each training session, a 5-minute rest allotted before resuming standard Taekwondo training. Post the 8-week training, both groups underwent a 2-week retention period with uniform training program.
Regular Taekwondo regimen without Elastic Resistance training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
kick velocity
Time Frame: 8 weeks
subjects executed three maximal RHKs with each leg, taking a 20-second rest between kicks. The best performance time was recorded.
8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Simple Eye-Hand Reaction Time Test
Time Frame: 8 weeks
For E-H reaction measurements, participants sit about 50 cm from the computer screen, with the screen placed 15 cm in front of and at the same height as the response panel. The response involves using the index finger of one hand, with the other hand resting beside the panel.
8 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Eye-Foot Reaction Time Test
Time Frame: 8 weeks
Simple Eye-foot (E-F) reactions were measured similarly, with the participant seated the same distance from the screen. The response panel is placed on the floor, positioned under the seated subject's foot. The response is made using the toe, while both hands rest on the desk and the other leg is positioned next to the panel.
8 weeks
Back-Leg-Chest Muscle Strength Dynamometry
Time Frame: 8 weeks
Participants, free from lifting restrictions, underwent Isometric Muscle Strength (IMS) testing using a back-leg-chest dynamometer (Saehan, SH5007, Masan 630-728, Korea). This device, correlated (r = 0.77, p <.001) with manual muscle tests 29, measures force applied to a spring, moving a pointer to indicate the exerted force. The dynamometer records up to 300 kg with 1 kg resolution, accurate to + 0.5 kg at 100kg. Subjects were instructed to stand with a 30-degree knee flexion and hip flexion, maintaining a proper lordotic curve, and then exert force using their legs and arms. The average of two strength measurements at each testing phase distinguished between learning and training effects. Participants controlled the exertion level, with to avoid discomfort.
8 weeks
Margaria-Kalamen Anaerobic Alactic Power Test
Time Frame: 8 weeks

The Margaria-Kalamen stair climb test measures an athlete's lower body peak power 30. Participants start 5 meters away from the first stair, quickly ascending on the researcher's signal, taking three steps at a time. Timers on the 3rd and 9th steps record the duration of the climb, starting and stopping as the participant hits these steps. The best performance time from three trials, each followed by a 20-second rest, is used. Anaerobic power, calculated in watts, is derived by multiplying the participant's weight by the stair height (16 steps) and gravitational acceleration (9.81 m·sec-1), and dividing by the time taken. This formula for computing anaerobic-alactic power follows 31:

Equation: Anaerobic Alactic Power (watts) = (body mass (kg) × distance (0.96 m) × 9.81m·sec-1) / time (sec-1).

8 weeks
10 m Sprint test
Time Frame: 8 weeks
In the 10 m sprint test (S-10m), participants completed three maximum-effort 10-meter sprints, timed using a Brower equipment (Wireless Sprint System, Draper, UT, USA). Photocells were placed at the start line (0 m) and at the 10 m mark, positioned 1 meter above the floor, aligning with the manufacturer's standard tripod height. Sprints were interspersed with 3-minute rest periods, and the fast sprint was recorded. This system validity and reliability have been confirmed, demonstrating an intraclass correlation coefficient between 0.92 and 0.98 and a coefficient of variation of 1.6% 32.
8 weeks
Jump Performance Test
Time Frame: 8 weeks
Lower limb power was evaluated using the counter movement jump (CMJ) test. Participants began each CMJ from a static standing position, executing a countermovement and then a rapid extension of the lower limb. They perform three maximal effort CMJ's, with 90-second rest intervals between jumps. The countermovement phase was self-selected, allowing athletes to use their preferred jumping technique. Participants were instructed to keep their trunk vertical and hands on their hips during jumps. Data was captured using an iPhone 11 Pro with My Jump app 27, recording at 240 frames per second.
8 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 (Actual)

January 2, 2024

Primary Completion (Actual)

March 10, 2024

Study Completion (Actual)

March 20, 2024

Study Registration Dates

First Submitted

August 20, 2024

First Submitted That Met QC Criteria

August 22, 2024

First Posted (Actual)

August 27, 2024

Study Record Updates

Last Update Posted (Actual)

August 27, 2024

Last Update Submitted That Met QC Criteria

August 22, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • #SA-EK-23-29

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

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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