- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05374889
Evaluation of the Contribution of Basketball-specific Target Shooting Exercises to Strength, Position Sense, Stability and Endurance in Young Basketball Players
May 10, 2022 updated by: Gulsum Mandir Comert, Istanbul University
The Effect of Open Kinetic Chain Proprioception Exercises on Joint Position Sense, Stability, Endurance and Strength in Adolescent Basketball Players
The aim of this study is to examine the effects of open kinetic chain proprioception exercises on joint position sense, strength, functional stability and endurance in adolescent basketball players
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Adolescent basketball players, aged 13-16, were randomly divided into two groups as exercise group (n = 11) and control group (n = 11).
Exercise group performed open kinetic chain functional proprioception exercises twice a week for 6 weeks.
Control group did not participate in any exercise program.
Before and after the exercise program all athletes were subjected to the proprioception test and isokinetic muscle strength test on the isokinetic dynamometer, closed kinetic chain upper extremity stability test and modified push-up test.
Study Type
Interventional
Enrollment (Actual)
22
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
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Istanbul, Turkey
- Istanbul Faculty of Medicine, Sports Medicine Department
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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
13 years to 16 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- being 13-16 years old
- being male
- playing basketball regularly
Exclusion Criteria:
- having any upper extremity muscle injury in the last 6 months,
- having a limitation in the shoulder girdle range of motion,
- having a shoulder, elbow, wrist dislocation 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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Exercise Group
Athletes were asked to throw the ball at predetermined targets in different positions with their eyes closed.
In the first exercise, the athlete was positioned 2 m from the target in a sitting position, facing the marked lines on the wall.
It was asked to make 3 trial shots with a basketball ball while the eyes were open, from the bottom up to the 3 lines on the wall.
Then the shots were made while the eyes were closed.
In the next exercise, it was requested to make 3 trial shots from the bottom up by looking at the same 3 lines marked in the supine position at the distance of 1 m from the target.
Then the shots were made with the eyes facing the ceiling.
The last exercise was in a standing position, from the line marked 5 m from the target to the basket, it was requested to make 3 trial free throw with eyes open to the basket.
Then, after each throw, the athlete was asked to turn around his own axis and continue to next throw, with eyes closed.
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basketball-specific target shooting in open kinetic chain
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No Intervention: Control Group
Control group did not participate in any exercise program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Proprioception test- Cybex-Humac NORM
Time Frame: 20 minutes
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Position-based proprioception test with Cybex-Humac NORM in 60 ̊ and 120 ̊ angles
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20 minutes
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Peak Torque & Peak Torque/Body Weight- Cybex-Humac NORM
Time Frame: 20 minutes
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Strength and endurance tests with Cybex-Humac NORM at 60°/sec and 180°/sec angular velocities
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20 minutes
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Closed kinetic chain upper extremity stability test
Time Frame: 5 minutes
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Recording the number of touches in 15 seconds
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5 minutes
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Modified push-up test
Time Frame: 10 minutes
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Recording the number of push-ups
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10 minutes
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gulsum Mandir Comert, M.Sc., Istanbul University
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)
January 2, 2020
Primary Completion (Actual)
March 15, 2020
Study Completion (Actual)
June 20, 2020
Study Registration Dates
First Submitted
May 4, 2022
First Submitted That Met QC Criteria
May 10, 2022
First Posted (Actual)
May 16, 2022
Study Record Updates
Last Update Posted (Actual)
May 16, 2022
Last Update Submitted That Met QC Criteria
May 10, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 2020/220
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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