Prevalence of Non-traumatic Musculoskeletal Disorders in the French Paragliding Pilots Population (EPPPAF)

March 5, 2024 updated by: University Hospital, Grenoble

The main objective is to determine the prevalence of non-traumatic pathologies in the paragliding population using the Nordic type questionnaire.

The paragliding pilots population frequently evoque pathologies, discomfort, or pain in the course of their practice. Said pain and discomfort, though unerelated any form of accident, seem to have an impact on the pilots' flying and their participation in daily life.

However, no epidemiological data are available in the literature. Investigators hypothesize the existence of non-traumatic disorders and it seems interesting to quantify the extent of the phenomenon. The results of this study might encourage the proposition of preventive measures in order to minimize a potential risk factor for paragliding accidents, and participation restrictions.

Study Overview

Detailed Description

In this cross-sectional descriptive epidemiological survey, investigators wish to quantify epidemiological parameters such as the prevalence of pathologies and their consequences in the activities of daily life.

For this purpose, an email containing the link to answer the online questionnaire will be sent to all the licensees.

The link of the questionnaire will be sent directly to all clubs in each league.

The main objective is to calculate the prevalence with descriptive statistics. The primary outcome is the prevalence of non-traumatic pathology in paragliding pilots that had registered to the French Paragliding federation (FFVL) in 2022.

The prevalence will be infered from the IRSST Standardised Nordic Questionnaire with the following formula : Prevalence = (FS4+FS6=yes and FS2=no ) divided by the total number of respondents.

FS4 item "Yes" = pain in the last 12 months FS6 item "Yes" = activity limitations) FS2 item "No" = Non-traumatic disorders

This corresponds to having felt pain in the body region indicated, at least once during the last 12 months, as well as a restriction of participation following this pain, but without having suffered trauma in the area.

For the secondary outcomes will aim at exploring several hypotheses related to personal and environmental factors that could be correlated to the incidence of the nontraumatic disorders. They will be calculated with bivariate descriptive statistics using the Pvalue.io software.

Study Type

Observational

Enrollment (Actual)

2475

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

      • Saint-Martin-d'Hères, France, 38400
        • Grenoble Alpes University - Faculty of Medecine - Departement of Physiotherapy

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

26000 people will be surveyed via the internet link. In 2021, according to the federal statistics of the FFVL accessible on the intranet of the FFVL, the number of practicing paraglider with a license was about 26000.

Description

Inclusion Criteria:

  • over 18 years old
  • Registered with the FFVL for the year 2022 and/or 2023
  • Paragliding in the year 2022 and/or 2023

Exclusion Criteria:

  • Adults not able to express their consent

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
registered
Paragliding pilots over the age of 18. Registered at the "Fédération Française de Vol Libre" (FFVL) in the year 2022 and/or 2023 Paragliding in the year 2022 and/or 2023
participants will complete the SNQ online. Estimated time of participation per person: 15 minutes to fill in the questionnaires

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of non-traumatic pathologies in the paragliding pilot population
Time Frame: Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)

The prevalence will be calculated using the IRSST's Standardised Nordic Questionnaire.

Prevalence = (FS4+FS6=yes and FS2=no ) on total number of respondents. This prevalence will be calculated on the Population Health, with the FS4 and FS6 items. And to be more specific about atraumatic pathologies, it is necessary to have answered "no" to the FS2 item. This corresponds to having felt pain in the body region indicated, at least once during the last 12 months, as well as a restriction of participation following this pain, but without having undergone trauma in the area concerned.

Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Correlations between prevalence, a body area, restriction of participation in paragliding and individual characteristics of participants
Time Frame: Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)
Correlation analysis (univariate and bivariate) between responses to different questions to test for a potential association between variables
Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)
Paragliders' beliefs about the origin of their pain.
Time Frame: Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)
Number of respondents with musculoskeletal disorder (FS9=yes)/total number of positive cases ((FS4+FS6=yes and FS2=no)
Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)
Prevalence of injuries sustained during a paragliding accident
Time Frame: Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)
Number of respondents with musculoskeletal disorder due to accident/total number of pain positive cases and participation restriction ((FS4+FS6=yes and FS2.3=yes)
Cross sectional study. Each participant is evaluated for 15 minutes (estimated time of completion of the questionnaire)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Thomas LATHIERE, Département de kinésithérapie, 175 avenue centrale 38400 Saint Martin d'Hères

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

March 12, 2023

Primary Completion (Actual)

June 4, 2023

Study Completion (Actual)

August 4, 2023

Study Registration Dates

First Submitted

March 7, 2023

First Submitted That Met QC Criteria

March 7, 2023

First Posted (Actual)

March 21, 2023

Study Record Updates

Last Update Posted (Actual)

March 7, 2024

Last Update Submitted That Met QC Criteria

March 5, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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