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Impact of Anthropometrics Data and of Physical Activity Level in Closed kineTic Chain Upper Extremity Stability Test (EPOLTEST)

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ClinicalTrials.gov Identifier: NCT04090632
Recruitment Status : Not yet recruiting
First Posted : September 16, 2019
Last Update Posted : September 16, 2019
Sponsor:
Information provided by (Responsible Party):
University Hospital, Brest

Brief Summary:
The purpose of this study is to evaluate impact of anthropometric criteria to CKCUEST score.

Condition or disease Intervention/treatment Phase
Shoulder Pain Diagnostic Test: Closed Kinetic Chain Upper Extremity Stability Test Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 82 participants
Intervention Model: Single Group Assignment
Intervention Model Description: This study is a monocentric interventional prospective study
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Impact of Anthropometrics Data and of Physical Activity Level in Closed kineTic Chain Upper Extremity Stability Test (CKCUEST) - EPOLTEST Study
Estimated Study Start Date : October 1, 2019
Estimated Primary Completion Date : October 1, 2020
Estimated Study Completion Date : October 1, 2020

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: closed kineTic chain upper Extremity Stability Test
Each patient receive the same intervention, the 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.
Diagnostic Test: Closed Kinetic Chain Upper Extremity Stability Test
Each patient receive the same intervention, the 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.




Primary Outcome Measures :
  1. 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. The outcome measure will be the mean of the three test realisation.


Secondary Outcome Measures :
  1. Global Physical Activity Questionnaire (GPAQ) [ Time Frame: Day 1 ]
    Global Physical Activity Questionnaire. It is a standardized questionnaire which evaluate the global physical activity. GPAQ takes into account both number and intensity of activity. There are 4 parts (profession activities,day to day ways of moving, hobbies, sedentarity) in total being 16 questions.



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Ages Eligible for Study:   18 Years to 25 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Aged to 18 to 25 years
  • Capacity to consent
  • Who has signed the consent

Exclusion Criteria:

  • fracture history or upper limb luxation
  • is not possible to do the test because of pain
  • pregnant or nursing
  • refuse to participate
  • guardianship or protection of vulnerable adult

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04090632


Contacts
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Contact: Marc Beaumont +33 (0)2 98 62 61 60 mbeaumont@ch-morlaix.fr

Locations
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France
CHRU de Brest Not yet recruiting
Brest, Finistère, France, 29200
Contact: Marc Beaumont    02.98.62.61.60    mbeaumont@ch-morlaix.fr   
Principal Investigator: Marc Beaumont         
Sponsors and Collaborators
University Hospital, Brest

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Responsible Party: University Hospital, Brest
ClinicalTrials.gov Identifier: NCT04090632     History of Changes
Other Study ID Numbers: 29BRC19.0147
First Posted: September 16, 2019    Key Record Dates
Last Update Posted: September 16, 2019
Last Verified: September 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: All collected data that underlie results in a publication
Supporting Materials: Study Protocol
Time Frame: Data will be available after the publication of result and ending fifteen years following the last visit of the last patient
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.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University Hospital, Brest:
CKCUEST
Physical activity
rehabilitation
Additional relevant MeSH terms:
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Shoulder Pain
Arthralgia
Joint Diseases
Musculoskeletal Diseases
Pain
Neurologic Manifestations
Signs and Symptoms