- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05291273
Influence of Anthropometric Data, Shoulder Complex Muscle Strength, and Abdominal-lumbar Endurance in Closed Kinetic Chain Upper Extremity Stability Test (EPOLTEST 2)
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
Status
Conditions
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Théophile Marchi
- Email: theophile.marchi@etudiant.univ-brest.fr
Study Contact Backup
- Name: Marc BEAUMONT
- Phone Number: 02 98 62 61 60
- Email: mbeaumont@ch-morlaix.fr
Study Locations
-
-
-
Brest, France, 29200
- Recruiting
- CHU de Brest
-
Principal Investigator:
- Marc BEAUMONT
-
Contact:
- Marc BEAUMONT
- Phone Number: 02 98 62 61 60
- Email: mbeaumont@ch-morlaix.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 29BRC22.0005
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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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