- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06269601
The Reliability of the Upper Limb Rotation Test in Adolescent Male Basketball Players
February 27, 2024 updated by: Birgül Dıngırdan, Hacettepe University
The objective of the study is to examine the reliability of the Upper Limb Rotation Test in adolescent male basketball players aged between 14 and 16.
According to the sample size calculation for the study, 51 athletes were included.
The Upper Limb Rotation Test was administered to the athletes twice, with a one-week interval.
The athlete was positioned in a plank stance with shoulder, elbow lateral epicondyle, greater trochanter, and ankle lateral malleolus making contact with the wall.
The athletes were instructed to perform a 90° abduction and 90° external rotation of the shoulder, accompanied by trunk rotation for a duration of 15 seconds.
The number of repetitions was recorded.
The tested side was the upper extremity in which the closed kinetic chain position was maintained.
The test was repeated three times, and the average of the results was calculated.
The Upper Extremity Rotation Test is a reliable assessment tool for evaluating performance in adolescent basketball players aged 14-16, particularly in relation to shooting skills.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The objective of the study is to examine the reliability of the Upper Limb Rotation Test in adolescent male basketball players aged between 14 and 16.
According to the sample size calculation for the study, 51 athletes were included.
The Upper Limb Rotation Test was administered to the athletes twice, with a one-week interval.
The athlete was positioned in a plank stance with shoulder, elbow lateral epicondyle, greater trochanter, and ankle lateral malleolus making contact with the wall.
The athletes were instructed to perform a 90° abduction and 90° external rotation of the shoulder, accompanied by trunk rotation for a duration of 15 seconds.
The number of repetitions was recorded.
The tested side was the upper extremity in which the closed kinetic chain position was maintained.
The test was repeated three times, and the average of the results was calculated.
The ICC (intraclass correlation coefficient) value, SEM (standard error of measurement), and MDC (minimal detectable change) values were calculated to assess the test-retest reliability of the evaluation tool.
A low SEM value indicates higher reliability of measurements.
The MDC value represents the smallest detectable change between two measurements.
Differences below this value are considered practically undetectable or statistically insignificant.
Study Type
Interventional
Enrollment (Actual)
51
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
-
-
-
Ankara, Turkey
- Hacettepe University
-
-
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:
- Male basketball players aged 14 to 18 years old.
- The athlete must have been engaged in basketball for a minimum of 3 years
- Athletes should be training at least three days per week.
Exclusion Criteria:
- The presence of coordination issues to an extent that hinders the compliance with the physiotherapist's instructions.
- Having undergone any orthopedic surgery in the upper extremities or spine within the last year.
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: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: adolescent male basketball players
14-16 years adolescent male basketball players
|
The athletes were instructed to perform a 90° abduction and 90° external rotation of the shoulder, accompanied by trunk rotation for a duration of 15 seconds.
The number of repetitions was recorded.
The tested side was the upper extremity in which the closed kinetic chain position was maintained.
The test was repeated three times, and the average of the results was calculated.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Reliability of the Upper Limb Rotation Test
Time Frame: through study completion, an average of 1 year
|
The Upper Limb Rotation Test was administered to the athletes twice with a one-week interval between the tests.
The athlete was positioned in a plank position with shoulder, elbow lateral epicondyle, greater trochanter, and ankle lateral malleolus touching the wall.
The athletes were instructed to perform a 90° shoulder abduction and 90° external rotation, along with a body rotation, for a duration of 15 seconds.
The number of repetitions was recorded.
The tested side involves the upper extremity where a closed kinetic chain position is maintained.
The test was repeated three times, and the average of the results was calculated.
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Birgül Dıngırdan, Master, Hacettepe University
- Study Director: Volga Bayrakcı Tunay, Proffessor, Hacettepe 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)
August 10, 2023
Primary Completion (Actual)
September 15, 2023
Study Completion (Actual)
September 15, 2023
Study Registration Dates
First Submitted
February 2, 2024
First Submitted That Met QC Criteria
February 20, 2024
First Posted (Actual)
February 21, 2024
Study Record Updates
Last Update Posted (Estimated)
February 28, 2024
Last Update Submitted That Met QC Criteria
February 27, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HÜ- FTR- BD- 02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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