Actively Recruiting
Professional Impact of Osteoarticular Trauma
Led by Hopitaux de Saint-Maurice · Updated on 2026-02-23
200
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Professional Impact of Osteoarticular Trauma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults who were treated for osteoarticular trauma at the hospital between June 2021 and June 2024
- Patients who were employed prior to the injury
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpitaux Paris Est Val-de-Marne - Service de rééducation orthopédique et traumatologie
Saint-Maurice, France, 94410
Actively Recruiting
Research Team
A
Auriane AS SLAMA
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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