- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04090632
Impact of Anthropometrics Data and of Physical Activity Level in Closed kineTic Chain Upper Extremity Stability Test (EPOLTEST)
January 15, 2021 updated by: University Hospital, Brest
Impact of Anthropometrics Data and of Physical Activity Level in Closed kineTic Chain Upper Extremity Stability Test (CKCUEST) - EPOLTEST Study
The purpose of this study is to evaluate impact of anthropometric criteria to CKCUEST score.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
82
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 Locations
-
-
Finistère
-
Brest, Finistère, France, 29200
- CHRU de Brest
-
-
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
16 years to 23 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
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: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / 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.
|
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.
|
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.
The outcome measure will be the mean of the three test realisation.
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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.
|
Day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 25, 2019
Primary Completion (Actual)
January 27, 2020
Study Completion (Actual)
January 27, 2020
Study Registration Dates
First Submitted
August 12, 2019
First Submitted That Met QC Criteria
September 13, 2019
First Posted (Actual)
September 16, 2019
Study Record Updates
Last Update Posted (Actual)
January 19, 2021
Last Update Submitted That Met QC Criteria
January 15, 2021
Last Verified
June 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 29BRC19.0147
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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