A cohort of healthcare workers in France
A Prospective Cohort of Healthcare Workers in France
This study is gathering information from healthcare workers in France to see how they can better protect their health and that of their patients, especially regarding COVID-19 prevention and vaccination.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 15000 (estimated) |
| Ages | 18 Years to 99 Years |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris) |
| Trial ID | NCT04870086 on ClinicalTrials.gov |
What this trial studies
ESPERES is a national prospective e-cohort study aimed at collecting information on healthcare workers (HCWs) in France. The study seeks to develop a community of HCWs eligible for future research, focusing on preventive measures for their health and that of their colleagues and patients. Participants will self-include and provide data through online questionnaires, with the first research focus being on COVID-19 prevention and vaccination. The cohort is open for inclusion until the end of the study, allowing for ongoing data collection and analysis.
Who should consider this trial
Good fit: Ideal candidates for this study are healthcare workers in various roles within healthcare settings, including administrative and support staff.
Not a fit: Patients who do not have internet access will not be able to participate in this study.
Why it matters
Potential benefit: If successful, this study could enhance preventive health measures for healthcare workers, improving their well-being and safety.
How similar studies have performed: Other studies focusing on healthcare worker health and preventive measures have shown promise, indicating that this approach is relevant and potentially beneficial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Legal age * Healthcare workers defined as individuals who currently work in a setting where individuals receive healthcare (i.e. individuals do not have to work directly with patients, but may have any role within a setting where individuals receive healthcare, such as administrative office, housekeeping, food service, etc.) * Agreeing to participate (digital consent) Exclusion Criteria: - No internet access
Where this trial is running
Paris
- Pitié-Salpêtrière - Charles Foix, AP-HP — Paris, France (Recruiting)
Study contacts
- Principal investigator: Florence Tubach, MD, PHD — Assistance Publique - Hôpitaux de Paris
- Study coordinator: Florence Tubach, MD, PHD
- Email: florence.tubach@aphp.fr
- Phone: 01 42 16 05 88
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.