Influence of Kinesio Taping on Muscle Activation, Muscle Strength and Performance of Young Football Athletes Jump

February 4, 2014 updated by: Daniela Ap. Biasotto-Gonzalez, University of Nove de Julho

INFLUENCE OF KINESIO TAPING ON MUSCLE ACTIVATION, MUSCLE STRENGTH AND PERFORMANCE JUMP IN YOUNG ATHLETES. CLINICAL STUDY, RANDOMIZED, PLACEBO-CONTROLLED AND DOUBLE BLIND

The objective of the project is to investigate the influence of application of Kinesio Taping in young athletes in football, muscle strength and muscle activation in the performance of the Single Leg Hop Test tests and Triple Hop Test methods: will be conducted a randomized, placebo-controlled and double-blind. 24 individuals will be athletes who fit the criteria for inclusion will be randomized into 2 groups (Placebo, Kinesio Taping Taping) and will be submitted to the tests of Single Leg Hop Test, Triple Hop Test, the isokinetic evaluation and electromyographic of Rectus Femoris dominant lower limb. Then the intervention shall be carried out with application of Kinesio Taping for activation of rectus femoris muscle group and placebo intervention Kinesio Taping with application of Kinesio Taping of transverse way the rectus femoris without tension in the Placebo group Taping. The volunteers will be re-evaluated 30 minutes after application of the technique and 12:0 am after with the same tests for that later can be compared the results obtained in each group. Analysis: will be achieved statistical tests and adopted a significance level of 5 percent

Study Overview

Status

Unknown

Conditions

Detailed Description

The method of bandage with Kinesio Taping created by Kenzo Kase in 1996, it is the application of a thin, elastic tape with a thickness similar to the epidermis, on the skin. Being that it can be stretched up to 140 of its original length making it elastic enough compared to the conventional bandages. Kenzo still claims that the tape is able to reduce pain, swelling, muscle spasms and prevent injury. As much as there is today a widespread use of this technique mainly in the context of sports and orthopedics, still lack reliable studies to support the theory described by this method. Objectives: to investigate the influence of application of Kinesio Taping in young athletes in football, muscle strength and muscle activation in the performance of the Single Leg Hop Test tests and Triple Hop Test methods: will be conducted a randomized, placebo-controlled and double-blind. 24 individuals will be athletes who fit the criteria for inclusion will be randomized into 2 groups (Placebo, Kinesio Taping Taping) and will be submitted to the tests of Single Leg Hop Test, Triple Hop Test, the isokinetic evaluation and electromyographic of Rectus Femoris dominant lower limb. Then the intervention shall be carried out with application of Kinesio Taping for activation of rectus femoris muscle group and placebo intervention Kinesio Taping with application of Kinesio Taping of transverse way the rectus femoris without tension in the Placebo group Taping. The volunteers will be re-evaluated 30 minutes after application of the technique and 12:0 am after with the same tests for that later can be compared the results obtained in each group. Analysis: will be achieved statistical tests and adopted a significance level of 5 percent.

Study Type

Interventional

Enrollment (Anticipated)

24

Phase

  • Phase 2
  • Phase 1

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

      • São Paulo, Brazil, 01415000
        • Recruiting
        • University of Nove de Julho
        • Contact:
          • Daniela Biasotto Goonzalez, Doctor
          • Phone Number: +5511999063166
          • Email: dani_atm@ig.com.br

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

15 years to 20 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Individuals aged between 15 and 20 years, Football players and Athletes who have body mass index (BMI) considered normal (between 20 and 25).

Exclusion Criteria:

  • History of lower limb musculoskeletal injuries in the last 6 months, history of lower limb and spine surgery in the last 6 months and BMI over 25 or less than 20.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Grupo A (Kinesio Taping)
Will be held the application of Kinesio Taping (Tex Gold) in the region of the rectus femoris dominant lower limb by a physical therapist trained in the technique (KT1 KT2 and) and with experience in this type of application to be designed without knowing in which group fits this patient. In the sequence, the athlete will be oriented to remain at rest for 30 min to get a better grip on the tape and one of the first tests and rest, only after this period will conduct a new evaluation of jump tests (single leg Hop test and Triple Hop Test) and, finally, a new test of strength in the isokinetic dinamomêtro in conjunction with the electromyographic assessment.
Application of Kinesio (Kinesio Tex Gold ®) of black color. The tape will be applied from proximal to distal, leaving the anterosuperior iliac spine Bottom, passing over the Rectus Femoris and ending in the region of the anterior tibia tuberosity with a voltage of 25 %.
Placebo Comparator: Placebo Taping
The volunteer will receive a Placebo application tape, being in this case the physical therapist will apply a strip of Kinesio Taping perpendicular to the muscle fibers of the rectus femoris of the dominant member of the individual.
The volunteer who is allocated at random in the placebo group will receive an application of Kinesio transverse way the rectus femoris muscle, in order to verify a possible placebo effect of application of tape.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hop Test
Time Frame: 1 year
The volunteer must position themselves in foot with unipodal support in the dominant lower limb behind a line that will be demarcated on the ground and jump as far as possible, without support in the contralateral limb or imbalance. The distance will be measured with a tape measure, from the starting point (line demarcated on the ground) until the most proximal point of the heel of the foot fell on the floor.
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Surface electromyography
Time Frame: 1 year
During isokinetic evaluation will also be carried out a study of the electrical activity of the rectus femoris muscle. For the capture of the electrical signal of that muscle will be used the acquisition system with 8 channels (EMG System of Brazil Ltda ®), composed of active electrodes with bipolar won 20 times amplification, analog filter pass band of 20 to 500 Hz and common mode rejection of 120 dB, and one of the channels will be enabled to use the force transducer (EMG System of Brazil Ltda ®). EMG signals are sampled with 2000 Hz frequency, scanned for AD conversion plate (analog-digital) with 16 bits of resolution.
1 year

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Isokinetic evaluation of knee Extensors
Time Frame: 1 year
Immediately after heating and evaluation of jumps, the volunteers will perform the test of maximum voluntary contraction (CVM). Being they, positioned sitting on the seat of the isokinetic dynamometer (4, Biodex) the dominant limb is positioned to 60° of knee flexion (with 0° corresponds to total knee extension) and attached to the seat by means of a dynamometer belt. The non-dominant lower limb will also be positioned with 100° of flexion of hip and will also be attached to the seat with a belt. The volunteers will also be attached to the seat of the dynamometer through two belts across his torso. During the tests the volunteers will be instructed to place his arms across the trunk and the dynamometer axis is positioned parallel to the center of the knee joint. The CVM test will consist in the execution of three isometric contractions of knee extensors of the non-dominant lower limb with duration of 5 seconds, the highest torque value obtained in the three contractions (peak torque).
1 year

Collaborators and Investigators

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

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.

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

January 1, 2014

Primary Completion (Anticipated)

October 1, 2014

Study Completion (Anticipated)

December 1, 2014

Study Registration Dates

First Submitted

February 4, 2014

First Submitted That Met QC Criteria

February 4, 2014

First Posted (Estimate)

February 6, 2014

Study Record Updates

Last Update Posted (Estimate)

February 6, 2014

Last Update Submitted That Met QC Criteria

February 4, 2014

Last Verified

December 1, 2013

More Information

Terms related to this study

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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