Accidentology and Traumatology Associated With Foiling in Brittany (TRAUMAF)

January 20, 2025 updated by: University Hospital, Brest

In the 2010s, the practice of water sports was turned upside down by the arrival of a new discipline: foiling. The number of sailors, particularly amateurs, is increasing every every year. The foil offers greater speed and height, and has therefore the accidents and injuries that result. injuries. But there are very few studies on the subject. The TRAUMAF study proposes to compare the distribution of the number of patients injured during water sports with and without the use of foils. The study also looks at patient management and the type of injury. The aim is to anticipate the management of these patients during periods of practice of these sports.

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Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • France
    • Finistère
      • Brest, Finistère, France, 29609
      • Douarnenez, Finistère, France, 29100
      • Morlaix, Finistère, France, 29600
        • Recruiting
        • Centre Hospitalier de Morlaix
        • Contact:
      • Quimper, Finistère, France, 29000
        • Recruiting
        • Centre Hospitalier Intercommunal De Cornouaille
        • Contact:
    • Morbihan
      • Lorient, Morbihan, France, 56100
        • Recruiting
        • GHBS Hôpital du Scorff
        • Contact:

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Any person of legal age, meeting the inclusion and non-inclusion criteria, presenting to an emergency department following a boating accident.

Description

Inclusion Criteria:

  • Patient of legal age
  • Patient not expressing refusal to participate in the study
  • Patient consulting an emergency room following a boating accident that occurred no more than 7 days previously
  • Patient able to complete a questionnaire

Exclusion Criteria:

  • Minor patient
  • Patients who are illiterate and/or do not understand French
  • Patient under legal protection

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluate the importance of foil-equipped craft in the occurrence of water-related injuries.
Time Frame: 12 months
Percentage of boating accidents involving foils.
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Provide the doctor in charge of the patient with objective data on the most likely lesions and their potential severity.
Time Frame: 12 months
Distribution of the frequency of different types of injury according to whether or not the foil was used (comparison between the two study groups).
12 months
Analysis of the type and location of lesions observed between the foil and no-foil groups.
Time Frame: 12 months
Comparison of the location of injuries observed between the foil and non-foil groups. Comparison of accident type (fall, cut, impact, etc.) between the two groups.
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Brest

Collaborators

Centre Hospitalier de Bretagne Sud
Centre Hospitalier des Pays de Morlaix
Hospital, Quimper
Hospital, Douarnenez

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)

January 15, 2025

Primary Completion (Estimated)

January 1, 2026

Study Completion (Estimated)

January 1, 2026

Study Registration Dates

First Submitted

October 16, 2024

First Submitted That Met QC Criteria

November 6, 2024

First Posted (Actual)

November 8, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 20, 2025

Last Verified

November 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 29BRC24.0152

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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