- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04780113
Evolution of Perceived Stress in General Practice Residents During COVID-19 Sanitary Crisis
April 21, 2022 updated by: Centre Hospitalier Eure-Seine
Evaluation of Evolution of Perceived Stress in General Practice Residents of Rouen and Caen During COVID-19 Sanitary Crisis
Over the last several years, distress among healthcare professionals is well described, and general practice residents are also affected.
Because of COVID-19 sanitary crisis, stress factors are increased, and that may cause anxiety, exhaustion, psychic distress, depression, addictions, or post traumatic stress.
Study Overview
Status
Completed
Conditions
Detailed Description
This prospective non-interventional study aims to evaluate via two questionnaires the evolution of perceived stress in general practice residents of two centres in France, Rouen and Caen.
The two questionnaires contain the Perceived Stress Scale, as well as items regarding socio-demographic data and stress factors.
The first questionnaire is to be distributed during the epidemic COVID-19 wave and the second questionnaire at the end of the epidemic COVID-19 wave.
Study Type
Observational
Enrollment (Actual)
185
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Évreux, France, 27015
- CH Eure-Seine
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Participants being general practice residents in Caen or Rouen
Description
Inclusion Criteria:
- Being a general practice resident in Rouen or Caen
- Participant informed and non-objection of him/her
Exclusion Criteria:
- Being on maternity leave or not working during the period concerned with the questionnaires
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evolution of perceived stress during the epidemic wave of COVID19 vs. at the end of the epidemic wave of COVID19
Time Frame: maximum 6 months, according to the evolution of the epidemic
|
The perceived stress will be evaluated using the Perceived Stress Scale.
This scale contains 10 items, with scores ranging from 0 to 40, with higher scores meaning a higher level of stress.
|
maximum 6 months, according to the evolution of the epidemic
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Description of general characteristics of residents and their feelings and experiences with the sanitary crisis
Time Frame: maximum 6 months, according to the evolution of the epidemic
|
This include socio-demographic characteristics, work-related information and potential stress factors
|
maximum 6 months, according to the evolution of the epidemic
|
|
Assessment of residents' profile stress according to their socio-demographic and working characteristics
Time Frame: maximum 6 months, according to the evolution of the epidemic
|
Identification of stress factors among residents
|
maximum 6 months, according to the evolution of the epidemic
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ségolène Guillemette, MD, General Practice Physician
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 25, 2021
Primary Completion (Actual)
September 24, 2021
Study Completion (Actual)
September 24, 2021
Study Registration Dates
First Submitted
March 1, 2021
First Submitted That Met QC Criteria
March 1, 2021
First Posted (Actual)
March 3, 2021
Study Record Updates
Last Update Posted (Actual)
April 22, 2022
Last Update Submitted That Met QC Criteria
April 21, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 2020-A03283-36
- CHES N°20/01 (Other Identifier: CH Eure-Seine)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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