- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06244030
The Effect of Core Stabilization Exercises in Female Wrestlers
April 2, 2024 updated by: Emine Atıcı, Okan University
The Effect of Core Stabilization Exercises on Trunk Muscle Strength, Upper Extremity Performance and Spinal Stability in Female Wrestlers
This study was planned to investigate the effect of core stabilization exercise program on trunk muscle strength, spinal stability and upper extremity performance in elite wrestling athletes.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
20
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
-
-
-
Istanbul, Turkey
- Istanbul Okan University
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-
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being between 14 and 21 years old and interested in wrestling
- Actively pursuing a life of wrestling
- Participate in training at least 4 days a week
- Wrestling in freestyle style.
- To confirm that there is no injury problem
- Being a licensed athlete
Exclusion Criteria:
- Experiencing any serious injury problems
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
The control group will not be given any exercise other than their own wrestling training program.
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|
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Experimental: Core Stabilization Group
The athletes in the core stabilization group will be applied a 15-20 repetition core stabilization exercise program 3 days a week for 6 weeks by the researcher.
The duration of the exercise program is planned not to exceed 30 minutes.
The values before and after the exercise program will be recorded.
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The athletes in the training group will be applied 15-20 repetitions of core stabilization exercise program 3 days a week for 6 weeks by the researcher.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of muscle strength
Time Frame: ''6 weeks''
|
An isokinetic dynamometer will be used for trunk muscle strength assessment.
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''6 weeks''
|
|
Medicine Ball Throwing Test
Time Frame: ''6 weeks''
|
This test is used to determine limb strength and power.
The materials needed will be a 2.5 kg medicine ball and a meter.
The individual will be asked to stand one step behind the starting line with the medicine ball in participant hand.
When the ball is at chest level, the individual will be asked to take a step and throw the ball as far as participant can.
Scoring will be done by measuring the distance the ball falls from the starting line
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''6 weeks''
|
|
Closed Kinetic Chain Upper Limb Test
Time Frame: ''6 weeks''
|
This test will measure upper extremity strength, endurance and closed kinetic chain stability.
Two athletic bands and a stopwatch will be needed for this test measurement.
Two pieces of athletic tape will be placed on the floor at 0.9 meter intervals.
The person will be asked to take a push-up position with participant hands open at the level of the band.
The person will be asked to move his/her hands from one band line to the other as fast as possible and touch each line by moving like a "wiper".
The touches will be counted for 15 seconds with a stopwatch.
Power scores will be determined by taking 68% of the person's body weight (the weight of the upper extremities, head and trunk at the upper level) in kilograms and multiplying it by the number of touches and dividing the result by 15.
|
''6 weeks''
|
|
Upper extremity Y balance test
Time Frame: ''6 weeks''
|
Functional dynamic postural balance assessments of individuals will be performed with the Y balance test.
Scores on the Y balance test kit are based on three directions will be recorded.
The Y balance Test kit will be used in medial, superolateral and inferolateral directions with 120° angles between them.
With the hand tested on the test kit in the push-up position with the tested hand in the center of the device at the junction of the angles, the participants will be asked to take the Y balance test box to the fingertip of the other hand to the farthest point they can reach and return it to its original position, and the distance they can reach will be measured in cm.
Measurements will be taken bilaterally with three repetitions.
After obtaining the mean values, normative values will be obtained by dividing the sum of right and left by two
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''6 weeks''
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Reach Test
Time Frame: ''6 weeks''
|
In this test researchers will ask participant to stand sideways next to a wall and make a fist with the arm close to the wall and keep it parallel to the floor.
researchers will mark the 3rd metacarpal head on the wall.
Meanwhile, researchers will ask the person to reach forward as far as they can without taking a step and mark the new 3rd metacarpal head.
Researchers will measure the distance between the marked lines at the beginning and end.
Researchers will make 3 attempts and finish the test by averaging the last 2 attempts
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''6 weeks''
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
February 5, 2024
Primary Completion (Actual)
March 15, 2024
Study Completion (Actual)
March 15, 2024
Study Registration Dates
First Submitted
January 29, 2024
First Submitted That Met QC Criteria
January 29, 2024
First Posted (Actual)
February 6, 2024
Study Record Updates
Last Update Posted (Actual)
April 3, 2024
Last Update Submitted That Met QC Criteria
April 2, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 011 (Nahrain Medical Research Collective (NMRC))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Will be shared when necessary
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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