Professional Impact of Osteoarticular Trauma

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHopitaux de Saint-Maurice

About this trial

This study aims to describe the medical, social, and organizational determinants of returning to work after an osteoarticular injury, particularly limb fractures.

Using observational data, the study will evaluate the modalities of returning to work within 12 months of the injury and analyze the factors influencing professional reintegration, including the severity of the injury, functional recovery, pain, professional characteristics, workplace accommodations, and administrative support measures such as recognition of disabled worker status.

The study will also explore the point at which the issue of returning to work is first raised with the patient during hospitalization, a period during which professional reintegration is often insufficiently anticipated. By identifying current practices and breaking points, this study aims to improve understanding of the pathways to returning to work in the context of the healthcare system and the world of work in France.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults who were treated for osteoarticular trauma at the hospital between June 2021 and June 2024

Patients who were employed prior to the injury

Disqualifiers

Death or major disability preventing completion of the questionnaire

Protected persons

Refusal to participate or no contact after follow-up

Patients who were unemployed prior to the trauma

Trial population

The study population consists of adult patients of working age who were employed prior to experiencing an osteoarticular trauma, including fractures of the limbs. Participants were followed at a tertiary hospital center and received care for osteoarticular trauma between June 2021 and June 2024. The study includes patients with available medical records allowing retrospective data extraction, as well as prospective collection of self-reported data through questionnaires, without any modification of standard clinical care.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

200 Participants
are grouped into 1 trial group
Group A: Working-Age Adults With Osteoarticular Trauma

Trial outcomes

Primary outcomes

1

Return-to-work rate within 12 months after osteoarticular trauma

Assess the professional impact of osteoarticular trauma by measuring the rate of return to work within 12 months of the trauma.

Time frame
Up to 12 months after trauma

Secondary outcomes

1

Time to return to work after osteoarticular trauma

Duration between the date of osteoarticular trauma and the date of return to work, expressed in days

Time frame
From inclusion to return to work (up to 12 months)
2

Workplace accommodations implemented after trauma

Implementation of workplace accommodations following osteoarticular trauma, including job adjustments, modified duties, or adapted working conditions

Time frame
Within 12 months after trauma, as reported at study inclusion
3

Recognition of disability status (RQTH)

Implementation of disability recognition status (Reconnaissance de la Qualité de Travailleur Handicapé, RQTH), a French administrative measure allowing access to workplace accommodations and vocational support.

Time frame
Within 12 months after trauma, as reported at study inclusion
4

Time to return to work and predictors (hazard ratios)

Time from inclusion to return to work will be measured in months. Time-to-event analysis will be performed using Kaplan-Meier survival curves. Medical, social, and occupational variables will be evaluated as predictors of time to return to work using Cox proportional hazards regression models. Results will be expressed as hazard ratios (HR) with 95% confidence intervals.

Time frame
Up to 12 months after trauma

Other outcomes

Sponsors and contacts

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