ClinicalTrials.Veeva

Menu

Patients Returning to Work After Acute Coronary Syndrome (ACS)

U

University Hospital, Strasbourg, France

Status

Unknown

Conditions

Acute Coronary Syndrome

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The literature is quite rich concerning the factors which influence the return to work after acute coronary syndrome. They can be divided into three categories: factors linked to the patient, those linked to the workstation and factors linked to an external intervention. A study published in 1992 evaluated a set of predictive factors for recovery one year after acute coronary syndrome and showed that the proportion of clinical factors accounted for 20%, functional factors for 27% but above all socio-economic factors for 45. %.

On the other hand, there are only a few studies that are interested in the return to work after acute coronary syndrome according to the management in occupational medicine, and in particular the realization or not of a pre-return visit.

The results of a survey published in 2016 show that the recommendations made during the return visit were significantly different depending on whether or not there was a pre-return visit and concerned all types of pathology.

In view of all of these elements, it seems important to the investigators to study the expected benefit of an early orientation towards occupational medicine via the pre-return visit, and to study the factors delaying or favoring the return to work. .

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18 years old
  • In professional activity during acute coronary syndrome (employee, civil servant, self-employed or looking for a job)
  • -Mastering the French language (knowing how to read and write French)
  • Agreeing to participate in the study and not having expressed his opposition to the reuse of his data for the purposes of this research

Exclusion criteria

  • Subject having expressed opposition to participating in the study
  • Inability to provide informed information about the subject (subject in an emergency situation, difficulty in understanding the subject, etc.)
  • Subject under safeguard of justice
  • Subject under guardianship or guardianship

Trial contacts and locations

1

Loading...

Central trial contact

Saïd CHAYER, PhD, HDR; Marc André GOLTZENE, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems