- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03494283
CrossFit's Injuries Study in Grand Nancy Clubs During 2018-2019 (CROSSFIT)
Prospective Epidemiological Study of Injuries Encountered in the Practice of CrossFit in Grand Nancy Clubs Over a Period of 8 Months.
CrossFit is a recent sport that has been democratized since the beginning of the 2000's in France. The 3 major studies of CrossFit injuries were conducted in the United States in 2014, Brazil in 2016 and the United States in 2017. They show a discrepancy in terms of injuries average, from 19.4% to 31% in relation to an upsurge in the number of CrossFit practitioners, the specific training or not of the coaches framing this activity, the practice or not in competition. The main locations of these wounds are highlighted at the shoulders, lumbar region and knees. In France, to date, no epidemiological studies have been conducted on this subject.
Hypothesis: High incidence of injuries related to a lack of framing, or bad practice and ignorance of CrossFit practitioners.
Objectives : Estimate the injuries incident due to the CrossFit practice over a 8-month period in an adult population who practice in clubs .
Research, among the anthropometric, sociodemographic, environmental, and the nature and frequency of practice and training sessions, those which are associated with the occurrence of injury in this cohort.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Nancy, France
- CHU
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Men and women
- 18 years and over
- Practicing Crossfit in a club of the Grand Nancy
- Information and non-opposition to research
Description
Inclusion Criteria:
Men and women
- 18 years and over
- Practicing CrossFit in a club of the Grand Nancy
- Information and non-opposition to research
Exclusion Criteria:
- Opposition to study
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
CrossFit injuries
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Improve and modify practice of the practicers and of the professionals who are framing to decrease the injury incidence.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
CrossFit's injuries follow-up questionaire
Time Frame: each month during 8 months
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Questionaire about musculoskeletal pain or discomfort due to CrossFit practice during the previous month .For a period of 8 months, in a population of adults practicing in a club, with musculoskeletal injuries questionaire.
A questionaire is given each month during 8 months concerning the previous month ( Questions about physical pain that they felt, practice modification... )This questionaire is not validated.
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each month during 8 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
CrossFit's injuries inclusion questionaire .
Time Frame: At inclusion
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One questionaire is given at inclusion for baseline demographic and baseline data (Age, sex , size , work's condition, practiced sports ) .
At the end of the study, the goal is to relate these data to the incidence of injuries found .This questionaire is not validated.
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At inclusion
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Collaborators and Investigators
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017-A02825-48
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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