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Impact of the COVID-19 Pandemic on the Quality of Psychological Life (COVID-PRO-IMPACT)

Impact of the COVID-19 Pandemic on the Quality of Psychological Life of Healthcare Professionals

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04375644
Acronym
COVIDPROIMPACT
Enrollment
1565
Registered
2020-05-05
Start date
2020-05-07
Completion date
2020-07-15
Last updated
2020-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid 19, Stress, Psychological

Brief summary

The COVID-19 pandemic is profoundly changing the way people live and work. After the health impact, it is the mental and psychological impact that reaches varying degrees in the entire world population. The previous Asian epidemics have had a lasting impact on the health professionals concerned. In France, no study has yet assessed the psychological impact of this health crisis on the level of health professionals. Investigators propose to study prospectively the evolution of the state of stress and anxiety of all the professionals practicing within the gynecology-obstetrics departments of 18 French hospitals. Investigators also hypothesize that the mental repercussions in terms of stress and anxiety within the same service could be different depending on the professional status and the place of exercise (the French regions being impacted in different ways). In addition to the epidemiological interest, the results of this study may help us to target regions and professionals who will need psychological support during and after this serious health crisis.

Interventions

OTHERQuestionnaires on psychological quality of life

Assessement of evolution of the psychological quality of life of health professionals during the confinement period linked to the COVID-19 pandemic by two questionnaires (one during the confinement period and the second one month after the end of the confinement period)

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* person over 18 * person exercising a profession in the health field * person having expressed his non-opposition

Exclusion criteria

* inability to understand the information given and the questionnaire * person deprived of liberty, person under guardianship.

Design outcomes

Primary

MeasureTime frameDescription
Stress state score, during the confinement periodAbout 10 minutes ( Questionnaire filling time)Stress state score, during the confinement period, established by a comparison VAS (visual analogue scale) compared to a period outside COVID-19 (from -5: considerable degradation to +5: considerable improvement, with 0: no change)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026