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Validation of a Scale of Well-being at Work

NCT02905071 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 226

Last updated 2025-12-22

No results posted yet for this study

Summary

The main objective of this work is to explore the psychometric properties of scale of well-being at work called "Serenat" in order to validate it. Secondary objectives are to study the influence of socio-demographic characteristics of the subjects on the results of Serenat and to describe the results on subjects monitored among an adult psychiatric population.

Conditions

  • Adjustment Disorder

Interventions

OTHER

filling of Serenat at baseline (T1)

Patients who consult occupational doctor complete the serenat questionnaire.The time taken to complete the serenat scale is about 5 minutes.

OTHER

Serenat at baseline T1 and 3 others questionnaires

Subjects who consult occupational doctor complete the 4 questionnaires.The time taken to complete the 4 questionnaires is about 15 minutes.

OTHER

filling of Serenat, HADS, STAY-Y and BDI at baseline T1

Patients who consult a psychiatrist in a stress anxiety unit complete the 4 questionnaires.

Sponsors & Collaborators

  • University Hospital, Lille

    lead OTHER

Principal Investigators

  • Dominique SERVANT, MD, PhD · University Hospital, Lille

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2017-11-26
Completion
2017-11-26

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02905071 on ClinicalTrials.gov