Measuring workplace satisfaction and well-being using visual analog scales
Validation of Visual Analog Scales to Measure SatisfactiOn and WELL-being at Work (SoWell-VAS)
University Hospital, Clermont-Ferrand · NCT05871411
This study is testing a simpler way to measure how happy and satisfied people feel at work to see if it helps them share their experiences better.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 120 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | University Hospital, Clermont-Ferrand (other) |
| Locations | 1 site (Clermont-Ferrand) |
| Trial ID | NCT05871411 on ClinicalTrials.gov |
What this trial studies
This observational study aims to validate visual analog scales designed to assess satisfaction and well-being in the workplace. It addresses the challenges of existing psychosocial risk questionnaires, which are often lengthy and complex, leading to low response rates. By simplifying the measurement process, the study seeks to provide a more efficient tool for evaluating occupational stress and related factors. The study will involve voluntary adults currently engaged in professional activities.
Who should consider this trial
Good fit: Ideal candidates for this study are voluntary adults who are currently employed.
Not a fit: Patients who are minors or those under legal protection may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a streamlined method for assessing workplace satisfaction and well-being, leading to improved occupational health interventions.
How similar studies have performed: While there have been various approaches to measuring occupational stress, the specific validation of visual analog scales in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All voluntary adults with a professional activity. Exclusion Criteria: * Minor * Person not volunteer to participate. * Protected adults (curatorship, guardianship, safeguard of justice)
Where this trial is running
Clermont-Ferrand
- CHU clermont-ferrand — Clermont-Ferrand, France (RECRUITING)
Study contacts
- Principal investigator: Frédéric Dutheil — University Hospital, Clermont-Ferrand
- Study coordinator: Lise Laclautre
- Email: promo_interne_drci@chu-clermontferrand.fr
- Phone: 334.73.754.963
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Validation, Visual Analogue Scale, Occupational Stress