Effect of Kinesio Taping on the Stability of Knee in Soccer Players (KT-Knee)

August 22, 2017 updated by: GEMMA V ESPÍ LÓPEZ, PhD, University of Valencia

Effect of Kinesio Taping and Proprioceptive Exercise on the Stability of Knee in Amateur Soccer Players

Objective: The general objective of this study is to determine the possible beneficial effect of the application of kinesiotaping, as well as the performance of proprioceptive exercises on parameters related to knee stability, such as the incidence of injuries, pain, static stability Or dynamics, and flexibility, in amateur soccer players, with a workload of 3 days per week plus the match.

Material and methods: Amateur soccer players are divided into 3 groups.

Group 1 (G1) performs proprioceptive exercises plus the application of kinesiotaping without tension in the knee.

Group 2 (G2) performs proprioceptive exercises plus the application of kinesiotaping with tension in the knee.

Group 3 (G3) is placed kinesiotaping with tension in the knee, without proprioception exercises.

The treatment will last four weeks and three evaluations, one before treatment, another at two weeks and the last one at the end of treatment.

Study Overview

Study Type

Interventional

Enrollment (Actual)

46

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

      • Valencia, Spain, 46010
        • Gemma Victoria Espí-López

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 to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Football players
  • Over 18 years with experience in this sport over 5 years

Exclusion Criteria:

  • Players with pathologies that prevented them from playing football normally
  • Recent serious injuries
  • Allergy to kinesiotaping
  • Impossibility to complete the study

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: Factorial Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Kinesio Taping placebo and exercises
kinesio placebo and exercises
Kinesio Taping placebo and exercises
Experimental: Kinesio Taping and exercises
kinesio with tension and exercises
Kinesio Taping with tension and exercises
Experimental: Kinesio Taping with tension
Kinesio Taping with tension

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
KOOS knee questionnaire
Time Frame: 4 weeks
4 weeks

Secondary Outcome Measures

Outcome Measure
Time Frame
Star Excursion Balance Test (SEBT)
Time Frame: 4 weeks
4 weeks
Unipedal Stance Test (UST)
Time Frame: 4 weeks
4 weeks
Sit and reach (Toe touch test)
Time Frame: 4 weeks
4 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Gemma V Espí-López, University of Physiotherapy

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)

July 18, 2017

Primary Completion (Actual)

August 22, 2017

Study Completion (Actual)

August 22, 2017

Study Registration Dates

First Submitted

July 14, 2017

First Submitted That Met QC Criteria

July 17, 2017

First Posted (Actual)

July 18, 2017

Study Record Updates

Last Update Posted (Actual)

August 23, 2017

Last Update Submitted That Met QC Criteria

August 22, 2017

Last Verified

August 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • ID0018

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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