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Clinical Trials/NL-OMON20811
NL-OMON20811
Other
Not Applicable

A nationwide multicentre observational study to investigate the fitness to perform ofaround-the-clock medical specialists.

Centre for Human Drug Research;Nederlandse Vereniging voor Heelkunde;Nederlandse Internisten Vereniging;Nederlandse Vereniging voor Obstetrie & Gynaecologie; Nederlandse Vereniging voor Kindergeneeskunde;Nederlandse Vereniging voor Anesthesiologie.0 sites1,000 target enrollmentTBD
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ConditionsA set of active round-the-clock medical specialists as well as active medicalregistrars, both male and female, will be assessed for their performance on theFTOP test.

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
A set of active round-the-clock medical specialists as well as active medicalregistrars, both male and female, will be assessed for their performance on theFTOP test.
Sponsor
Centre for Human Drug Research;Nederlandse Vereniging voor Heelkunde;Nederlandse Internisten Vereniging;Nederlandse Vereniging voor Obstetrie & Gynaecologie; Nederlandse Vereniging voor Kindergeneeskunde;Nederlandse Vereniging voor Anesthesiologie.
Enrollment
1000
Status
Other
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Centre for Human Drug Research;Nederlandse Vereniging voor Heelkunde;Nederlandse Internisten Vereniging;Nederlandse Vereniging voor Obstetrie & Gynaecologie; Nederlandse Vereniging voor Kindergeneeskunde;Nederlandse Vereniging voor Anesthesiologie.

Eligibility Criteria

Inclusion Criteria

  • •Eligible subjects must meet all of the following inclusion criteria:
  • •1\. Subjects are around\-the\-clock medical specialists or medical registrars, employed at the participating hospitals within one of the following medical specialties:

Exclusion Criteria

  • •Eligible subjects must meet none of the following exclusion criteria:
  • •1\. A condition that in the opinion of the investigator would complicate or
  • •compromise the study, or the well\-being of the subject (e.g. decreased vision or limited range of motion in the forearm or wrist)

Outcomes

Primary Outcomes

Not specified

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