Effects of Proprioceptive Training on Neurofunctional Control and Ankle Sprains Incidence

April 14, 2016 updated by: Gabriela Souza de Vasconcelos, Federal University of Rio Grande do Sul

Effects of Proprioceptive Training on Neurofunctional Control and Ankle Sprains Incidence in Fencers: a Randomized Controlled Trial

The aim of this study is to investigate the influence of a 12-week proprioceptive training program on the neurofunctional control and the incidence of ankle sprains in fencing athletes. The study will be developed in six stages: familiarization, pre intervention, intervention, post intervention follow-up of three and six months. In the pre intervention stage will evaluate muscle strength inverters, everter, dorsal plantar flexors and ankle flexors through the isokinetic dynamometer; the reaction time of these muscles during Lunge Test; neuromuscular control during the Star Excursion Balance Test and performance in Drop Vertical Jump Test. In the intervention athletes will perform proprioceptive training for 12 weeks, three times a week, lasting 30 minutes. In the post intervention, the follow up of three to six months will be held the same pre intervention of the tests and recording the incidence of injuries occurred during the study. The expected result at the end of the study is to improve all variables, increasing the performance of athletes and decreasing the incidence of ankle sprains.

Study Overview

Status

Unknown

Conditions

Detailed Description

Fencing is an agility sport, with higher incidence of injuries in the lower limbs, with the ankle sprain the most prevalent. Injury prevention is very important to improve performance and reduce time off of athletes. Proprioceptive training programs can be added to the training of athletes, since in addition to the easy application and low cost, proprioception serves to stabilize the joint, preventing injuries. Therefore the aim of this study is to investigate the influence of a 12-week proprioceptive training program on the neurofunctional control and the incidence of ankle sprains in fencing athletes. The study will be a randomized clinical trial, with fencing athletes from 14 to 25, a multi-sport club of Porto Alegre/RS, and developed in six stages: familiarization, pre intervention, intervention, post intervention follow-up of three and six months. The first step will be to familiarize themselves with the force of testing and registration of injuries in the previous year. In the pre intervention stage will evaluate muscle strength inverters, everter, dorsal plantar flexors and ankle flexors through the isokinetic dynamometer; the reaction time of these muscles during Lunge Test; neuromuscular control during the Star Excursion Balance Test and performance in Drop Vertical Jump Test. In the intervention athletes will perform proprioceptive training for 12 weeks, three times a week, lasting 30 minutes. In the post intervention, the follow up of three to six months will be held the same pre intervention of the tests and recording the incidence of injuries occurred during the study. For statistical analysis, the data will be presented as mean and standard deviation and submitted to the Shapiro-Wilk test, ANOVA will be held for repeated measures and post hoc Bonferroni to determine differences. The effect size is calculated using Cohen's d test.o significance level is 0.05. The expected result at the end of the study is to improve all variables, increasing the performance of athletes and decreasing the incidence of ankle sprains.

Study Type

Interventional

Enrollment (Anticipated)

18

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

    • Rio Grande do Sul
      • Porto Alegre, Rio Grande do Sul, Brazil, 90160181

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

14 years to 30 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • practicing fencing at least a year
  • have between 14 and 30 years.

Exclusion Criteria:

  • be in physical therapy or participating in prevention programs
  • have damage to lower limbs that compromise the tests

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
Experimental: Intervention: Proprioceptive Training

The intervention will be the implementation of a proprioceptive training program for the fencing athletes in the intervention group.

In this study the training program will be developed for 12 weeks and will be applied during the heating of the athletes, three times a week and the duration of each session is 30 minutes. Each week will be chosen three of the 14 exercises adapted for fencing athletes, and preferably one of each category. The categories have exercises with different levels of difficulty and can change the exercises occur by different proposed levels or the complexity of the exercise by changing category. The training program will be implemented by the same evaluator over the 12 weeks.

In this study the training program will be developed for 12 weeks and will be applied during the heating of the athletes , three times a week and the duration of each session is 30 minutes. Each week will be chosen three of the 14 exercises adapted for fencing athletes , and preferably one of each category.
Placebo Comparator: Control
The control group will not make the intervention and will continue with the usual training fencing.
The control group will not make the intervention and will continue with usual training fencing.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Onset muscle
Time Frame: 12 weeks
The muscular reaction time will be assessed by electromyography during Lunge Test.
12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle Strength
Time Frame: 12 weeks
The muscle strength of ankle will be assessed by isokinetic dynamometer.
12 weeks
Star Excursion Balance Test (SEBT)
Time Frame: 12 weeks
The SEBT will be used to measure the dynamic neuromuscular control.
12 weeks
Drop Vertical Jump Test (DVJT)
Time Frame: 12 weeks
The DVJT be used to assess the height of the heels, from surfaces 30, 40 and 50cm .
12 weeks
Cumberland Ankle Instability Tools (CAIT)
Time Frame: 12 weeks
The CAIT will be used to assess whether the ankle has istabilidade
12 weeks
Injury questionnaire
Time Frame: 12 weeks
This questionnaire will be used to assess the number of injuries and to joints they occurred.
12 weeks

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

April 1, 2016

Primary Completion (Actual)

April 1, 2016

Study Completion (Anticipated)

April 1, 2016

Study Registration Dates

First Submitted

April 6, 2016

First Submitted That Met QC Criteria

April 14, 2016

First Posted (Estimate)

April 15, 2016

Study Record Updates

Last Update Posted (Estimate)

April 15, 2016

Last Update Submitted That Met QC Criteria

April 14, 2016

Last Verified

April 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • 436620

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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