Ignite Creation Date:
2025-12-24 @ 11:34 PM
Ignite Modification Date:
2025-12-25 @ 9:22 PM
Study NCT ID:
NCT06267456
Status:
COMPLETED
Last Update Posted:
2024-02-28
First Post:
2024-01-30
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
The Reliability of ULRT in Overhead Athletes and Its Relationship With Selected UEPT
Sponsor:
Hacettepe University
Organization:
Study Overview
Official Title:
The Reliability of Upper Extremity Rotation Test in Overhead Athletes and Its Relationship With Selected Upper Extremity Performance Tests
Status:
COMPLETED
Status Verified Date:
2024-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Upper Extremity Rotation Test is a new test the evaluates 90-90 position, which is one of the requirements for overhead throwing. The aim of the study was to evaluate the reliability of the Upper Extremity Rotation Test in overhead athletes and the relationship between the Closed Chain Upper Extremity Stability Test and the Upper Quarter Y Balance Test.
Detailed Description:
Upper Extremity Rotation Test is a new test the evaluates 90-90 position, which is one of the requirements for overhead throwing. The aim of the study was to evaluate the reliability of the Upper Extremity Rotation Test in overhead athletes and the relationship between the Closed Kinetic Chain Upper Extremity Stability Test and the Upper Quarter Y Balance Test. Upper Extremity Rotation Test was found to be reliable in overhead athletes. Upper Extremity Rotation Test showed high reliability in overhead atheletes. There was no correlation between the Upper Exremity Rotation Test and the Upper Quarter Y Balance Test. A moderate corelation was found between the Upper Extremity Rotation Test and Closed Kinetic Chain Upper Extremity Stability Test.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: