- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06361654
Effect of Muscular Imbalance Between Flexors and Extensors of the Fingers and Wrist on Upper Limb Injuries in Climbers (CRIMPER)
Effect of Muscular Imbalance Between Flexors and Extensors of the Fingers and Wrist on Upper Limb Injuries in Climbers, a Longitudinal Study.
Climbing is a booming sport with an increasing number of participants. When practicing this sport, there is a muscular imbalance between the flexor and extensor systems (especially in the fingers), with the flexors of the fingers exerting greater force than the extensors. In addition, upper limb injuries, particularly the fingers, are very common.
The study will be carried out on club-licensed climbers, as they are better supervised. They will be recruited through requests sent to various clubs. The measurements will be taken during different climbing sessions, after the warm-up.
The study will include measurements on different climbers. Informed consent and personal data will be collected from the climbers before the measurements are taken. The strength values of the flexors and extensors of the fingers and wrist will be measured using a dynamometer. The climbers will then continue their usual training for 1 year. For 1 year after the measurements, the climbers will be contacted every month by telephone to collect the different injuries they may have suffered in relation to climbing, as well as the number of hours they have spent climbing in the past month. After 1 year, the annual number of hours of climbing and the annual number of injuries can be calculated for each climber. Injury is defined as any medically diagnosed lesion of the musculoskeletal system of the upper limb or pain that prevents the practice of a sport whose aetiology is climbing. These data are used to calculate the "athlete exposure" (A-E), i.e. the incidence of injury per 1000 hours of practice. As the study population is large, this allows for variations in exposure between subjects.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: timothee gillot, phd
- Phone Number: +33 0232880671
- Email: timothee.gillot@chu-rouen.fr
Study Contact Backup
- Name: deborah lebedieff
- Email: deborah.lebedieff@chu-rouen.fr
Study Locations
-
-
Normandie
-
Rouen, Normandie, France, 76031
- Recruiting
- Rouen, University Hospital
-
Contact:
- timothee gillot, phd
- Phone Number: +33 0232880671
- Email: timothee.gillot@chu-rouen.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
- A male or female climber who has been a member of a climbing club for at least 1 year;
- Have a level of 6a "on sight" or higher;
- Fluent in spoken and written French;
- Over 18 years of age.
Exclusion Criteria:
- Declaration of a medically diagnosed upper limb injury at the time of testing;
- Presence of any pathology that prevents climbing or taking finger or wrist measurements;
- Volunteers for whom it is impossible to collect data by telephone.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Athlete exposure
Time Frame: through study completion, an average of 1 year
|
- Athlete exposure (A-E): the incidence of climbing-related upper limb injuries reported over 1000 climbing hours (declarative).
The number of injuries and climbing hours will be collected by telephone every month for 1 year;
|
through study completion, an average of 1 year
|
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/0135/OB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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