- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05754463
The Effect Of Plyometric Training On Balance And Proprioception In Different Branches Athletes (Plyometric)
The Effect Of Plyometric Training On Balance And Proprioception
The aim of this study is to investigate the effect of plyometric training on balance and proprioception in athletes in different branches.
54 athletes participated in the study. Two groups were included as 27 athletics and 27 karate groups. Plyometric training was applied to the athletes participating in our study, 2 days a week for 6 weeks, after 20 minutes of warming up and stretching movements before each training. Sociodemographic characteristics of the athletes were recorded. Dynamic balance Y balance test and static balance Stroke balance test; sense of proprioception was evaluated with Angle reproduction test.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ankara, Turkey
- The Effect of Plyometric Training on Balance and Proprioception in Different Branches Athletes
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Being a licensed athlete in the province of Tokat
- Being an athlete who trains regularly
- To be healthy, between the ages of 12 and 18
- Volunteering to work.
Exclusion Criteria:
- Presence of any disturbance that may affect balance and balance reactions,
- Musculoskeletal injury in the last 6 months,
- Presence of previous musculoskeletal surgery,
- Pregnancy,
- Having an acute or chronic illness or injury that will limit performance in training or a match,
- Calcification or other bone and joint problems,
- Using cigarettes, alcohol, and drugs that affect balance.
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 |
|---|---|
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Experimental: athletes
Plyometric training was applied to the athletes (Group 1) (n=27) participating in our study, 2 days a week for 6 weeks, after 20 minutes of warming up and stretching movements before each training.
Sociodemographic characteristics of the athletes were recorded.
Dynamic balance test was applied with Y balance test and static balance was applied with strok balance test before and after plyometric training.
Proprioception assessment was applied with kinematic angle reproduction test before and after plyometric training.
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Investigating the effect of plyometric training on balance and proprioception in athletes in different branches
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Active Comparator: karate
Plyometric training was applied to the karate practitioners (Group 2) (n=27) participating in our study, 2 days a week for 6 weeks, after 20 minutes of warming up and stretching movements before each training.
Sociodemographic characteristics of the athletes were recorded.
Dynamic balance test was applied with Y balance test and static balance was applied with strok balance test before and after plyometric training.
Proprioception assessment was applied with kinematic angle reproduction test before and after plyometric training.
|
Investigating the effect of plyometric training on balance and proprioception in athletes in different branches
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Plyometric training
Time Frame: 2 days a week for 6 weeks
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The individuals included in our study were divided into two groups by a simple randomization method.
Plyometric training was applied to the both groups (athletes and karate practitoners).
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2 days a week for 6 weeks
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Y balance Test
Time Frame: 6 weeks
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It is used to dynamically measure balance.
This test includes extensions in the anterior, posterolateral, and posteromedial directions. .
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6 weeks
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Stroke Balance Test
Time Frame: 6 weeks
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The athlete warms up for 10 minutes.
The athlete stands comfortably on both feet, his hands are on his hips.
The athlete raises the right leg and places the sole of the right foot on the edge of the left kneecap.
The tester gives the command "GO", starts the stopwatch, and the athlete raises the heel of the left foot and stands on the toes.
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6 weeks
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Proprioception assessment (Eyes-closed kinematic angle reproduction test)
Time Frame: 6 weeks
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Participants in this test were asked to stand on one leg.
The goniometer support point is placed lateral to the knee joint, one side parallel to the trochanter major line, and the other side along the lateral malleola line with the knee extended.
In order to get results, the goniometer is fixed.
The participant is asked to bring the knee from extension to flexion and stop the knee at a target angle of 30 degrees of flexion at a very low speed (about 10 degrees per second).
The participant is asked to remain in this position for 4 seconds and then to extend the knee.
The participant is asked to close their eyes and flex the knee to a target degree.
In this way, the degree of deviation of the participant is recorded.
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6 weeks
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Collaborators and Investigators
Sponsor
Collaborators
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 (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
- 40
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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