- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02739308
Effects of Proprioceptive Training on Neurofunctional Control and Ankle Sprains Incidence
Effects of Proprioceptive Training on Neurofunctional Control and Ankle Sprains Incidence in Fencers: a Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Rio Grande do Sul
-
Porto Alegre, Rio Grande do Sul, Brazil, 90160181
- Recruiting
- Gabriela Souza de Vasconcelos
-
Contact:
- Gabriela Vasconcelos, Student
- Phone Number: 555195372276
- Email: gabih-vasconcelos@hotmail.com
-
Contact:
- Claúdia Lima, Dr
- Phone Number: 555199964747
- Email: claudia.lima@ufrgs.br
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
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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