Shoulder Endurance Test: Normative Values in a Population of Female Handball Players Aged 14 to 18 in Intensive Training Structures. (SET-HANDBALL)

December 23, 2024 updated by: University Hospital, Brest

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

Not yet recruiting

Study Type

Interventional

Enrollment (Estimated)

40

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 Contact

Study Locations

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:

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

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: 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

This is where you will find people and organizations involved with this study.

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 (Estimated)

January 1, 2025

Primary Completion (Estimated)

January 1, 2026

Study Completion (Estimated)

January 1, 2026

Study Registration Dates

First Submitted

August 30, 2024

First Submitted That Met QC Criteria

December 23, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 23, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 29BRC23.0027

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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