- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03872973
The Effect of Visual Input in Athletes With Chronic Ankle Instability
The Effect of Visual Input on Balance, Neural Feedback, Function and Running Mechanics in Athletes With Chronic Ankle Instability
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Lateral ankle sprain (LAB) is one of the most common musculoskeletal injuries of 15% of all injuries reported in all sports.Chronic ankle instability (CAI) is characterized by life-long persistent symptoms in 40% of people with recurrent LAB sprain.
It has been reported that there is a change in sensorimotor function in the activity of individuals with CAI, and they are more dependent on visual information in balance parameters on one leg.While the somatosensory input was clinically feasible; The obstruction of the visual input has been limited in two ways, the eyes being fully open or fully enclosed.However, this changing dynamic has provided a means for the prevention of visual input during more sporty maneuvers, to directly reach compensatory neuroplastic sequelae after injury and to function in a functional way to train the neuromuscular system.This technological innovation makes this possible by reducing the visual input without completely eliminating it.This innovation, called stroboscopic goggles technology, provides a mechanism to disrupt to any degree between eyes closed and open in the visual system.
Stroboscopic vision, characterized by intermittent vision obstruction, can be a clinical tool that allows clinicians to study sensory feedback in a progressive manner without fully seeing visual information. So use stroboscopic goggles to prevent visual information, you can improve the functionality by emphasizing the somatosensor information.In particular, visual manipulations can significantly influence the healthy adult electrocortical dynamics and balance control by triggering the contradiction between visual adult, vestibular and proprioceptive inputs.
The aim of this study, which was planned for this purpose, will be to evaluate the effects of neuromuscular exercises performed on stroboscopic environment on equilibrium, neural feedback and running mechanics.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Merkez
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Nevşehir, Merkez, Turkey, 50300
- Serkan UZLAŞIR
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- To have at least 5 years active athletes in any sports branch.
- The first sprain history of individuals should be inflammatory symptoms (pain, swelling) at least 1 year before the study,
- Individuals should have unilateral ankle sprain,
- The newest sprain must have occurred 3 months before or after the date of commencement,
- Individuals must have at least 2 times a feeling of instability within 6 months,
- Individuals should not have any ankle fractures in the past
- Individuals should have undergone no surgical procedure to affect the sensorimotor function in the lower extremity.
- IDFAI (Identification of Functional Ankle Instability Questionare) score is above 11,
- FAAM (Foot and Ankle Ability Measure) score less than 90%,
- FAAM-S (Foot and Ankle Ability Measure Sport Scale) score should be less than 80%.
Exclusion Criteria:
- Individuals who are not active athletes for at least 5 years in any sports branch.
- First sprain history of individuals with inflammatory symptoms (pain, swelling) at least 1 year before the study.
- The absence of unilateral ankle sprain by individuals.
- The most recent buckling is that it did not take place 3 months before or after the date of commencement.
- Individuals should not have a feeling of instability for at least 2 times within 6 months.
- People experience ankle fractures in the past.
- Individuals have undergone surgery to affect the sensorimotor function in the lower extremity.
- IDFAI (Identification of Functional Ankle Questionability) score not more than 11.
- FAAM (Foot and Ankle Ability Measure) score not less than 90%. FAAM-S (Foot and Ankle Ability Measure Sport Scale) score not less than 80%.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Training Group
Neuromuscular training will be performed in this group for 6 weeks.
|
The experimental group will perform neuromuscular exercise for 6 weeks. The other experimental group will perform neuromuscular exercises with strobe glasses. |
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Experimental: Strobe Group
This group will perform neuromuscular training for 6 weeks with a strobe glasses.
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The experimental group will perform neuromuscular exercise for 6 weeks. The other experimental group will perform neuromuscular exercises with strobe glasses.
Stroboscopic glasses, which is characterized by intermittent vision obstruction, is a clinical tool that allows clinicians to examine sensory feedback in a progressive manner without fully seeing visual information.
|
|
No Intervention: Control Group
This group will not perform any neuromuscular training program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
FAAM (Foot and Ankle Ability Measure),
Time Frame: 8 weeks
|
Pre-test evaluation will be done.
After the end of neuromuscular training for 6 weeks, the final test will be evaluated.
This value will be saved as %.
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8 weeks
|
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Ankle ROM
Time Frame: 2 weeks
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The two bars of Optojump are placed on the treadmill with a speed of 3.5m / sec and the foot strokes, imbalance and heel strokes will be recorded and the normal joint movements of the ankle with the Myo-motion device will be recorded.
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2 weeks
|
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Balance
Time Frame: 2 weeks
|
Static and dynamic balances of athletes before and after neuromuscular training will be evaluated.
Center of pressure area (COP) foot pressure point shall be evaluated in mm.
And İt is defined as a measure indicative of the time and/or distance a subject spent away from a central point.
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2 weeks
|
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EEG (Electroencephalography)
Time Frame: 2 weeks
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The theta and beta waveform of EEG values of people will be measured during the static and dynamic balance evaluation.
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2 weeks
|
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FAAM-S (Foot and Ankle Ability Measure Sport Scale)
Time Frame: 8 weeks
|
Pre-test evaluation will be done.
After the end of neuromuscular training for 6 weeks, the final test will be evaluated.
The Sports subscale is scored the same as FAAM (Foot and Ankle Ability Measure) 4 being 'no difficulty at all' to 0 being 'unable to do'.
The score on each item are added together to get the item score total.
The number of items with a response is multiplied by 4 to get the highest potential score.
If the subject answers all 8 items the highest potential score is 32, if one item is not answered the highest potential score is 28, if two are not answered the highest potential score is 24, etc.
The item score total is divided by the highest potential score.
This value is multiplied by 100 to get a percentage.
A higher score represents a higher level of physical function.
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8 weeks
|
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BMI (Body Mass Index)
Time Frame: 2 weeks
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Body mass index will be calculated before neuromuscular training.
It will be evaluated in kg/m2.
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2 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Serkan UZLAŞIR, Nevşehir Hacı Bektaş Veli University Sports Science Laboratory
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
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
- 2018.14.163
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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