The Impact of Outdoor Sports Practice on the Well-Being of Disabled People

The Impact of Outdoor Sports Practice on the Well-Being of Disabled People : a Cross-Sectional Study

Survey of the members of the French Handisports Federation (FFH) practicing outdoor sports.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

This is a national cross-sectional study to investigate the impact of outdoor sports practice on the well-being and self-esteem of people with disabilities.

The study is based on a survey of FFH members practicing outdoor sports. The survey will be distributed between October and November 2023 via the federation's internal communication system. Data will be collected on outdoor sports activity, psychological impact and barriers to practice.

Analyses will be made between able-bodied and disabled members, between types of disability, and between types of outdoor sport practiced (water, land and air).

Analysis will be based on anomysed data and will respect the MR004 methodology.

Study Type

Observational

Enrollment (Estimated)

500

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 Locations

      • Paris, France
        • Recruiting
        • French Handisport Federation
        • Contact:
          • Emmanuel Buchoud

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Members of the French Handisport Federation practicing outdoor sports

Description

Inclusion Criteria:

  • Being a member of the French Handisport Federation between September 2022 and August 2023
  • Practicing outdoor sports

Exclusion Criteria:

  • Persons who have objected to be contacted by e-mail

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
All subjects with impairments
On outdoor sports practice activity, barriers to practice, impacts on well-being.
All subjects without impairments
On outdoor sports practice activity, barriers to practice, impacts on well-being.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact of my outdoor sports on my well-being
Time Frame: Baseline
Rating Scale : 1 (low) to 10 (high)
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact of my outdoor sports on my self-esteem
Time Frame: Baseline
Rating Scale : 1 (low) to 10 (high)
Baseline

Collaborators and Investigators

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

Investigators

  • Study Director: Vincent T. Carpentier, MD-MSc, Institut de Sante Parasport Connecte Synergies
  • Study Director: Eric Perera, PhD, Montpellier University - SANTESIH
  • Study Director: Emmanuel Buchoud, French Handisport Federation

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)

September 25, 2023

Primary Completion (Estimated)

November 30, 2023

Study Completion (Estimated)

December 31, 2024

Study Registration Dates

First Submitted

September 7, 2023

First Submitted That Met QC Criteria

September 13, 2023

First Posted (Actual)

September 15, 2023

Study Record Updates

Last Update Posted (Estimated)

October 9, 2023

Last Update Submitted That Met QC Criteria

October 6, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2023-004

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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