- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05111587
Epidemiology of Injuries Caused by the Practice of Artificial Structure Climbing (EPITRAUMABLOC)
Epidemiology of Injuries Caused by the Practice of Artificial Structure Climbing: Prospective Cohort Study in Réunion Island
This study aims to precisely describe epidemiology of injuries than occur during practice of climbing in artificial structure.
Each participant will complete questionnaires in order to identify injuries. The first questionnaire will be completed at the moment of the inclusion and the second questionnaire will be completed if participant has injuries every 3 months until month 12.
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Saint-Pierre, Réunion
- Climbing structure
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- person who practices artificial structure climbing
Exclusion Criteria:
- person who refuses to participate
- person under tutorship or curatorship
- person who cannot read and write
- person who wants to leave Reunion Island within 12 months
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
injury relapse or not
Time Frame: at month 3
|
injury relapse is classified as early relapse if occurs within 2 months after the healing, as late relapse if occurs from 2 months to 12 months after the healing or as very late relapse if occurs after more 12 months.
|
at month 3
|
|
record of exposure to injury
Time Frame: at month 3
|
Training volume will be recorded by level of practice (leisure practice, club practice and competition practice)
|
at month 3
|
|
location of injury
Time Frame: at month 3
|
at month 3
|
|
|
laterality of injury
Time Frame: at month 3
|
at month 3
|
|
|
mechanism of injury
Time Frame: at month 3
|
it will be identified as a traumatic injury or an overuse.
Traumatic injury is due to an acute identified event.
An overuse is due to repetitive train injury.
|
at month 3
|
|
circumstance of injury occurence
Time Frame: at month 3
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at month 3
|
|
|
diagnosis of injury
Time Frame: at month 3
|
diagnosis will be claissified according to the OSICS 10 classification
|
at month 3
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021/CHU/27
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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