- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05536778
Shoulder Endurance Assessment in Upper Limb Athletes
Relation Between Different Tests Aimed to Assess Shoulder Endurance in Upper Limb Athletes
The objective of this study is to explore the relationship between two different "fatigue tests" (Xco Endurance Test and Shoulder Endurance Test) and strength/endurance of shoulder rotators muscles, measured with an isokinetic device.
The tests will be organized during two different sessions, in a randomized order. One session will be dedicated to isokinetic evaluation. The other one will include the performance of the two functional tests.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Liège
-
Liege, Liège, Belgium, 4000
- University of Liege
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age between 18 and 28 years
- To practice an overhead sports, at least 5 hours a week
Exclusion Criteria:
- Any shoulder surgery history
- Any shoulder pain
- Any shoulder injury during the last 6 months
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Other
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder rotators strength
Time Frame: through study completion, 6 months
|
Shoulder rotators strength (IR, ER) will be measured with isokinetic dynamometer
|
through study completion, 6 months
|
|
Shoulder rotators work
Time Frame: through study completion, 6 months
|
Shoulder rotators work (IR, ER) will be measured with isokinetic dynamometer
|
through study completion, 6 months
|
|
Shoulder Endurance Test
Time Frame: through study completion, 6 months
|
Time until exhaustion (in seconds) will be measured
|
through study completion, 6 months
|
|
Xco Endurance Test
Time Frame: through study completion, 6 months
|
Time until exhaustion (in seconds) will be measured
|
through study completion, 6 months
|
Collaborators and Investigators
Sponsor
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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Shoulder endurance assessment
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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