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NCT Number: NCT07419217

Professional Impact of Osteoarticular Trauma

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hôpitaux Paris Est Val-de-Marne - Service de rééducation orthopédique et traumatologie

Saint-Maurice, 94410, France

Location status: Recruiting

Location contact

Auriane AS SLAMA

CONTACT

[email protected]

+33 143967556 ext. +33607317969

About this study

Osteoarticular trauma, particularly limb fractures, is a major public health problem and frequently affects young people of working age. These injuries often result in prolonged interruption of professional activity and significant socioeconomic consequences. Returning to work is a key step in the rehabilitation process after trauma, but it is influenced by a wide range of medical, social, and organizational factors.

Medical determinants include the severity of the injuries, functional limitations, pain, and long-term sequelae. In addition, professional and social factors such as the type of job, employer support, the possibility of workplace accommodations, and administrative procedures related to disability recognition can strongly influence the terms of return to work. Beyond clinical recovery, the organization of care pathways and coordination with occupational health services also play a decisive role in professional reintegration.

This observational study aims to describe the pathways to return to work after osteoarticular trauma in the French context. It will assess the rate of return to work within 12 months of the trauma, as well as the time taken to resume professional activity. It will also analyze the medical, social, and professional factors associated with returning to work, including workplace accommodations and the implementation of administrative measures related to disability.

The study will further explore the point at which the issue of return to work is first raised with patients during hospitalization. This period is a critical phase during which professional reintegration is often insufficiently anticipated. By identifying current practices and the timing of these discussions, the study aims to better characterize existing gaps in the early anticipation of professional return.

By providing descriptive data on the determinants of return to work after osteoarticular trauma, this study aims to improve understanding of professional reintegration pathways and guide the development of future strategies that promote earlier anticipation and enhanced coordination of return to work within healthcare systems and the world of work.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults who were treated for osteoarticular trauma at the hospital between June 2021 and June 2024
  • Patients who were employed prior to the injury

Exclusion criteria

  • 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

Treatment and study plan

Primary outcomes

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

    Time frame: Up to 12 months after trauma

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

Secondary outcomes

  1. Time to return to work after osteoarticular trauma

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

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

  2. Workplace accommodations implemented after trauma

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

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

  3. Recognition of disability status (RQTH)

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

    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.

  4. Time to return to work and predictors (hazard ratios)

    Time frame: Up to 12 months after trauma

    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.

  5. Timing of return-to-work discussion during hospitalization

    Time frame: From hospital admission to hospital discharge (up to 30 days).

    Time (in days) from hospital admission to the first discussion regarding return to work with the patient will be recorded during the hospitalization period.

Study contacts

Contact information is provided by the study sponsor or research team.

Auriane AS SLAMA

CONTACT

[email protected]

+33 143967556 ext. +33607317969

Sponsors and collaborators

Lead sponsor

Hopitaux de Saint-Maurice

Other

Registry information

Official study title

Professional Impact of Osteoarticular Trauma: Retrospective Study on Return to Work, Accommodations, and Recognition in the Workplace

Acronym: IPTO

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Feb 18, 2026
Registry last updated
Feb 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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