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Clinical Trials/NCT02905071
NCT02905071
Completed
Not Applicable

Study of the Psychometric Properties of the Scale of Well-being at Work: The Serenat Study

University Hospital, Lille1 site in 1 country226 target enrollmentNovember 1, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adjustment Disorder
Sponsor
University Hospital, Lille
Enrollment
226
Locations
1
Primary Endpoint
Serenat scale
Status
Completed
Last Updated
4 months ago

Overview

Brief 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.

Detailed Description

This is a cross sectional survey. 200 subjects were selected among people having consulted an occupational doctor to validate the scale in the general population (study 1), and 50 subjects among a psychiatric population for the ancillary study (study 2). The Serenat Scale is a self-report questionnaire composed of 20 items. All items are scored on a four point Likert scale ranging from 0 (strongly disagree) to 3 (strongly agree) resulting in a range of 0 to 60. The 20 items are related to different domains. 10 items explore psychological balance at work: relaxation (item 1), sleep quality (item 2), concentration (item 3), form (item 4), sense of security (item 5), satisfaction (item 6), quality of relationships and contacts at work (item 7), voltage or aggressiveness (item 8), optimism for the future from a professional point of view (item 9), life balance (item 10). 10 items are related to working conditions and organization of work: comfort of the working environment (item 11), time constraint (item 12), sense of competence (item 13), decision latitude (item 14), interest at work and variety of tasks (item 15), recognition (item 16), professional support (item 17), communication and transfer of information (item 18), human conflict (item 19), satisfactory work schedules (item 20).

Registry
clinicaltrials.gov
Start Date
November 1, 2013
End Date
November 26, 2017
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Lille
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • agree to participate, exert a professional activity for at least 3 months at the time of inclusion, consult an occupational doctor or go to consultations related to stress and anxiety, read and be able to respond to the scale,

Exclusion Criteria

  • not be acting on work stoppage, nor pregnant, be capable of consent, not benefit from any legal protection regime and not be deprived of freedom.

Outcomes

Primary Outcomes

Serenat scale

Time Frame: At baseline (T1)

For Group 1, Group 2, Group 3: The Serenat Scale is a self-report questionnaire composed of 20 items. All items are scored on a four point Likert scale ranging from 0 (strongly disagree) to 3 (strongly agree) resulting in a range of 0 to 60. The 20 items are related to different domains. 10 items explore psychological balance at work. 10 items are related to working conditions and organization of work.

Secondary Outcomes

  • Serenat scale(one week after baseline (T2))
  • Hospital Anxiety and Depression Scale (HADS)(At baseline (T1))
  • State-Trait Anxiety inventory (STAI-Y)(At baseline (T1))
  • The Beck depression inventory (BDI-21)(At baseline (T1))

Study Sites (1)

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