Effectiveness of an Exercise Protocol on Alteration of Knee Joint Position Sense in Futsal Players

October 25, 2016 updated by: Guido Fabián Gómez Chiguano, University of Alcala
This research presents a randomized clinical trial which evaluates the effectiveness of an exercise protocol on the knee-joint repositioning in futsal players related to a post-match muscle fatigue. Our hypothesis is the improvement of sensation in a knee in joint position before and after the match when performing our exercise program.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

34

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

    • Madrid
      • Collado Villalba, Madrid, Spain, 28400
        • Guido Gómez

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

16 years to 24 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

Must have three years of experience in futsal Must be Licensed players

Exclusion Criteria:

lower limb injuries

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
It consists on only a regular training performance
Experimental: Experimental
It consists on performing the protocol which includes 6 strength, agility and balance exercises together with the regular training. The exercise program has to be performed twice a week during 6 weeks
The multi-intervention exercise protocol consists in a performance of agility, strength and balance exercises. It has to be fulfilled during 6 weeks (twice a week) before the regular training performance. The exercises should be done for almost 15 minutes approx. There will be 6 exercises in total: squat with toe raise, one-leg squats, single-leg balance (throwing a ball with a partner), vertical jumps, hamstring exercise, quick forwards and backwards sprints.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Joint Position Sense
Time Frame: up to 6 weeks after the end of the intervention
Joint Position Sense: Pictures of the knee joint repositioning of the participant are taken. The camera is placed perpendicularly 2 m from the knee joint and 65 cm from the ground. As references, 4 markers are placed in the lower extremity. The participant is seated with his feet dangling and his eyes closed. The dominant leg of the participant is passively carried by the examiner to 45 ° knee flexion. The participant is asked to maintain that position for 10 seconds. After that examiner returns the leg of the player to initial position in a passive way. The participant is then asked to change the position of the leg in an active way to the target position and maintain it for 4 seconds. After that he should return to the initial position. This exercise should be done 3 times. In each position a photograph is taken and then all of them are measured by Autocad which specifies the angles. The absolute angular error, the relative angular error and the variable angular error are measured.
up to 6 weeks after the end of the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical jump heigh
Time Frame: up to 6 weeks after the end of the intervention

Vertical jump height: for this, computer software "HSC-Kinovea" must be used. To perform the jump, hands should be placed on hips and the maximum impulse should be taken with both legs in order to take off from the ground. Each participant performs 5 preparatory jumps and then another 5 jumps (as high as possible). These 5 last jumps are the ones that will be analyzed. The height of the best jump is obtained through the formula mentioned above.

The flight time of these 5 jumps will be recorded with a camera that films 240 frames per second (Canon PowerShot SX700 HS). The analysis of the data is done with the software "Kinovea 0.8.15 for Windows" that measures the time difference between the first frame in which both feet are taking off the floor and the frame in which only one or both feet land. This measurement allows us to relate the height of each jump with muscle fatigue

up to 6 weeks after the end of the intervention
Perceived exertion rate
Time Frame: up to 6 weeks after the end of the intervention

Perceived exertion rate is obtained through the Borg Scale for Perceived Exertion (Borg's 6 to 10 Rating of Perceived Exertion Scale) with the aim of relating the subjective perception of the effort with objective measures of muscle fatigue. It is a discrete quantitative variable.

Borg Scale for Perceived Exertion will be given to the participants at the end of each match. It consists of a list of numbers from 6 to 20 which are related to subjective expressions of effort (no effort: 6, extremely light: 7-8, very light: 9, light 11 moderate: 13, hard 15, very hard 17, extremely hard: 19, maximum effort: 20). The participant will be asked how they felt during this physical activity (in relation with the effort). The collected data will be related to the numeric value.

up to 6 weeks after the end of the intervention

Collaborators and Investigators

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

June 1, 2016

Primary Completion (Actual)

October 1, 2016

Study Completion (Actual)

October 1, 2016

Study Registration Dates

First Submitted

June 8, 2016

First Submitted That Met QC Criteria

June 16, 2016

First Posted (Estimate)

June 17, 2016

Study Record Updates

Last Update Posted (Estimate)

October 27, 2016

Last Update Submitted That Met QC Criteria

October 25, 2016

Last Verified

October 1, 2016

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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