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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05145777
Other study ID # 8334
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 30, 2021
Est. completion date June 2022

Study information

Verified date November 2021
Source University Hospital, Strasbourg, France
Contact Marc André GOLTZENE, MD
Phone 33 3 88 11 64 66
Email marcandre.goltzene@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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. .


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date June 2022
Est. primary completion date June 2022
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de Pathologie Professionnelle - Médecine de Travail - Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Study of the contribution of the pre-return visit to the return to work after acute coronary syndrome 1 month
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