- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05112380
Fatigue Test With an XCo
Elaboration of an External Rotators Fatigue Test With an XCo
Study Overview
Detailed Description
At first, the reliability of the Xco endurance test will be assessed in sedentary adults. Then, the reliability of the test will be assessed in overhead athletes. The experimentation will include two sessions. During those sessions, the impact of fatigue (induced by the test) on rotator cuff muscles strength and on functional test performance (Single Arm Medicine Ball Throw) will be assessed. A time of 7 to 10 days will be provided between the two sessions.
To perform the XCo endurance test, the participant will be seated on a chair, arm at 90° of abduction (in frontal plane), elbow flexed at 90 degrees and positioned on a wooden support. From a 90 degrees of abduction and a neutral position of rotation, the participants will be asked to realise an external rotation movement of 90 degrees and then to go back to the starting position as many times as possible at a speed of 140 bpm. Mechanical stops (the wall and an adjustable height table) will be added to make sure that the participants respected the entire range of motion. After adjusting the position, it will be asked to the participants to perform 2 repetitions of 5 movements at 140 bpm (in eccentric and concentric) to get familiar to the rhythm. Thirty seconds of rest will be provided between the 2 repetitions to avoid the appearance of fatigue before the test.
Then, the participants will begin the test. The objective of the test will be to perform the movement as long as possible. The test will be stopped if the volunteers is not able to maintain the rhythm or to do the movement anymore. The Modified Borg Scale will be used to be sure that each subject was really exhausted when the test was stopped. For that purpose, each of them will have to quantify their level of exhaustion on the scale (maximum score = 10) every 30 seconds.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Liège, Belgium, 4000
- Université de Liège
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Practice of an overhead sport at least 5 hours a week (overhead athletes group)
- Not practice an overhead sport (sedentary adults)
Exclusion Criteria:
- History of shoulder pain
- Shoulder pain
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Sedentary adults
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The subjects will perform the test two times, with 7-10 days between the two sessions
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Overhead athletes
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The subjects will perform the test two times, with 7-10 days between the two sessions
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Time to exhaustion
Time Frame: 10 days
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10 days
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Shoulder rotators strength
Time Frame: 10 minutes
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10 minutes
|
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Distance reached with Single Arm Medicine Ball Throw
Time Frame: 10 minutes
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10 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Camille Tooth, ULiège
Publications and helpful links
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Fatigue XCo
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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