Actively Recruiting

Age: 18Years - 80Years
All Genders
ID05871411

Validation of Visual Analog Scales to Measure SatisfactiOn and WELL-being at Work (SoWell-VAS)

Led by University Hospital, Clermont-Ferrand · Updated on 2024-08-06

120

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of Visual Analog Scales (EVAs) to measure satisfaction and well-being at work, addressing psychosocial risks like workload, autonomy, burnout, anxiety, effort-reward balance, and work addiction. Current questionnaires used to assess these risks can be very long and complex, leading to low response rates and inconsistent answers. This study aims to validate shorter, quicker, and more uniform scales that provide precise and continuous data for better analysis. Participants in this observational study will complete EVAs designed to assess various psychosocial factors at work, including burnout, anxiety, job demand, job control, social support, effort-reward imbalance, work addiction, and life satisfaction. These measurements will be taken at inclusion and one week later. Sociodemographic, occupational, and lifestyle data such as work hours, alcohol and tobacco use, physical activity, stress levels, and sleep quality will also be collected once at inclusion. During the study, participants will complete questionnaires and scales that evaluate their psychosocial work environment and related health factors. Researchers will monitor changes in burnout, anxiety, work demands, and support over one week to validate the new scales. The total participation involves completing assessments at two time points, helping to better understand occupational stress and well-being using these new measurement tools.

CONDITIONS

Brief Title

Validation of Visual Analog Scales to Measure SatisfactiOn and WELL-being at Work (SoWell-VAS)

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All voluntary adults with a professional activity
Not Eligible

You will not qualify if you...

  • Minor
  • Person not volunteer to participate
  • Protected adults (curatorship, guardianship, safeguard of justice)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Diagnostic Evaluation

Duration - 1 day

Participants provide baseline information on work-related well-being and other health and lifestyle factors.

1 visit (in-person or remote) at inclusion

Long-term Monitoring

Duration - 1 week

Participants complete follow-up assessments to measure changes in well-being one week after inclusion.

1 follow-up visit (in-person or remote) approximately one week after inclusion

Trial Site Locations

Total: 1 location

1

CHU clermont-ferrand

Clermont-Ferrand, France

Actively Recruiting

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Research Team

L

Lise Laclautre

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Validation of visual analogue scales to assess occupational stress compared to the Karasek questionnaire: A cross sectional study.

Maëlys Clinchamps, Bruno Pereira, Martial Mermillod...

https://pubmed.ncbi.nlm.nih.gov/41666222