Influence of Anthropometric Data, Shoulder Complex Muscle Strength, and Abdominal-lumbar Endurance in Closed Kinetic Chain Upper Extremity Stability Test (EPOLTEST 2)

February 4, 2025 updated by: University Hospital, Brest

A previous study of the Closed Kinetic Chain Upper Extremity Stability Test (EPOLTEST) in a population aged 18 to 25 years isolated 3 main factors influencing the CKCUEST score: upper extremity span, weight, and sex of the individual. A predictive equation for the CKCUEST score was thus established and to date has a capacity to determine the real score of approximately 51%.

The results of this first study show that a certain number of variables have not been studied.

The purpose of this study, EPOLTEST 2, is to take into account the variables already studied on a larger population (18-50 years old) and to add an assessment of shoulder muscle strength and abdominolumbar endurance.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

247

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 Contact Backup

Study Locations

      • Brest, France, 29200
        • Recruiting
        • CHU de Brest
        • Principal Investigator:
          • Marc BEAUMONT
        • Contact:

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

18 years to 50 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Aged to 18 to 50 years
  • Capacity to consent
  • Who has signed the consent

Exclusion Criteria:

  • Fracture history or upper limb luxation < 1 year
  • Pain or discomfort that prevents the test from being performed
  • History of abdominal surgery or hernia < 1 year
  • Pregnant or nursing
  • Refuse to participate
  • Guardianship or protection of vulnerable adult

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 Closed Kinetic Chain Upper Extremity Stability Test (CKCUEST). The CKCUEST is a functional test which assess shoulder's stability. Patient is in push-up position, with 91 cm between his hands. His body is straight and his foots are squeeze. patient has to touch his hand with his other one and returns in the initial position. Then, patient repeats this movement with his other hand, etc, during 15 secondes. The CKCUEST score is the movement's number performed.
The prone bridge test also known as the "plank" or "hover" measures the muscular endurance of the abdominal muscles. Subjects will start in the "down" push up position with their feet together and their hands shoulder width apart. When the test starts the subject will push up to the prone bridge position so they are resting on their hands and toes making sure they maintain a straight line from the shoulders through the hips to the knees. The outcome measure will be the time where the subject stay in this position.
Maximum isometric force of the external and internal rotators and abductors/adductors measured by a dynamometer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Closed Kinetic Chain Upper Extremity Stability Test (CKCUEST) score
Time Frame: Day 1
Closed Kinetic Chain Upper Extremity Stability Test/ The CKCUEST is a functional test which assess shoulder's stability. Patient is in push-up position, with 91 cm between his hands. His body is straight and his foots are squeeze. Patient has to touch his hand with his other one and returns in the initial position. Then, patient repeats this movement with his other hand, etc, during 15 secondes. The CKCUEST score is the movement's number performed. Three tests are performed. The outcome measure will be the mean of the score of the three tests realisation.
Day 1
Anthropometric data
Time Frame: Day 1
Measurement of the subject's weight in kilograms
Day 1
Anthropometric data
Time Frame: Day 1
Measurement of the subject's height in centimeters
Day 1
Anthropometric data
Time Frame: Day 1
Measurement of the subject's BMI in kg/m^2
Day 1
Anthropometric data
Time Frame: Day 1
Measurement of the subject's upper extremity length in centimeters
Day 1
Anthropometric data
Time Frame: Day 1
Measurement of the subject's upper extremity span in centimeters
Day 1
Anthropometric data
Time Frame: Day 1
Measurement of the subject's distance between acromion and radial styloid of the right upper limb in centimeters
Day 1
Anthropometric data
Time Frame: Day 1
Measurement of the subject's distance between olecranon and radial styloid of the right upper limb in centimeters
Day 1
Muscular strength of the shoulder complex
Time Frame: Day 1
Maximum isometric force of the external and internal rotators and abductors/adductors measured by a dynamometer in Newton.
Day 1
Abdominal-lumbar stability
Time Frame: Day 1
The prone bridge test also known as the "plank" or "hover" measures the muscular endurance of the abdominal muscles. Subjects will start in the "down" push up position with their feet together and their hands shoulder width apart. When the test starts the subject will push up to the prone bridge position so they are resting on their hands and toes making sure they maintain a straight line from the shoulders through the hips to the knees. The outcome measure will be the time where the subject stay in this position.
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 (Actual)

June 8, 2022

Primary Completion (Estimated)

December 8, 2025

Study Completion (Estimated)

December 8, 2025

Study Registration Dates

First Submitted

March 11, 2022

First Submitted That Met QC Criteria

March 21, 2022

First Posted (Actual)

March 22, 2022

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 4, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 29BRC22.0005

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All collected data that underlie results in a publication

IPD Sharing Time Frame

Data will be available after the publication of result and ending fifteen years following the last visit of the last patient.

IPD Sharing Access Criteria

Data access requests will be reviewed by the internal committee of Brest University Hospital. Requestors will be required to sign and complete a data access agreement.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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