- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06754774
Shoulder Endurance Test: Normative Values in a Population of Female Handball Players Aged 14 to 18 in Intensive Training Structures. (SET-HANDBALL)
Shoulder Endurance Test : Valeurs Normatives Chez Une Population De Handballeuses De 14 À 18 Ans En Structures Intensives D'entrainement. SET-HANDBALL
57% of young female handball players experience shoulder pain. This pain is likely to affect training and performance, but most players continue to play despite it. Endurance of the shoulder lateral rotators is a risk factor for sports such as handball. A protocol for applying the Shoulder Endurance Test (SET) to assess the endurance of the lateral rotators of the shoulder has been proposed, but the authors stress the need for further research to validate this test in different sports and for different populations.
The purpose of the study was to determine normative values for the Shoulder Endurance Test in female handball players aged 14 to 18 in intensive training facilities.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: LE ROY Marc
- Phone Number: 0298017916
- Email: marc.leroy1@univ-brest.fr
Study Locations
-
-
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Brest, France, 29200
- CHU de Brest
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Contact:
- LE ROY Marc
- Phone Number: 02 98 01 79 16
- Email: marc.leroy1@univ-brest.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Girls aged 14 to 18 playing handball Handballers training at the Pôle Espoirs or the Centre Labellisé d'Entrainement 29 Players of legal age who have given their consent Signature of consent by parents for underage players
Exclusion Criteria:
Refusal of the minor to take part, even if the legal representatives want the player to take part in the study Refusal to perform the test
Pain preventing the test from being performed
All musculoskeletal conditions affecting the upper limb less than 6 months old.
Shoulder and cervical spine surgery less than 6 months old.
All musculoskeletal conditions affecting the cervical spine less than 6 months old.
Player under legal protection (guardianship/trusteeship) or deprived of liberty
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
All subjects will perform the same tests.
|
Each patient receive the same intervention, the Shoulder Endurance Test (SET).
The Shoulder Endurance Test assesses the endurance of the shoulder muscles in an open kinetic chain.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
To determine normative values for the Shoulder Endurance Test in female handball players aged 14 to 18.
Time Frame: Day 1
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessing intra-examiner reliability
Time Frame: two months after the test
|
Evaluate intra-examiner reliability: on site SET score versus SET score on video analysis (carried out 2 months after the face-to-face test).
|
two months after the test
|
|
Assessing inter-examiner reliability
Time Frame: two months after the test
|
Evaluate inter-examiner reliability: SET score for operator 1 versus operator 2 based on analysis of videos
|
two months after the test
|
|
Determine the SET score on the non-dominant arm
Time Frame: Day 1
|
Day 1
|
|
|
Evaluate the effort perceived during the test
Time Frame: Day 1
|
Borg scale after SET
|
Day 1
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Other Study ID Numbers
- 29BRC23.0027
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
product manufactured in and exported from the U.S.
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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