Behaviour and Experience of Communities Healthcare Professionals Facing the SARS CoV-2 (COVID-19) Epidemic (COVecu)

March 26, 2026 updated by: Assistance Publique - Hôpitaux de Paris

Behaviour and Experience of Communities Healthcare Professionals Facing the SARS CoV-2 Epidemic

The purpose of this study is to identify behaviours and experiences of communities healthcare professionals (doctors, nurses and physiotherapists) in the management of the SARS-CoV 2 epidemic by identifying the impact of the epidemic on their work, their personal life and the difficulties they had experienced.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Detailed Description

Given the overcrowding in hospital services, the management of the health crisis linked to the SARS-CoV-2 epidemic relies in particular on the Territorial Professional Health Communities, which include doctors, nurses and physiotherapists. The challenge of caring for patients in a health system described as suffering, raises questions about the experience of the epidemic at all levels of action. To our knowledge, there is no information to date on the experience of the health crisis of urban health professionals in terms of the impact on their professional and personal lives and the difficulties encountered.

Using a mixed, cross-sectional, observational and multicentric methodology, the aim of this study, lasting a total of 12 months, is to identify the impact on professional and personal life as well as the difficulties experienced by doctors, nurses and physiotherapists working in private practice in connection with a CPTS involved in the management of the health crisis.

Semi-directive interviews, lasting a maximum of 45 minutes, will be carried out with doctors, nurses and physiotherapists integrated into a CPTS and digitally recorded audio digitally and then transcribed literally and in full. They will be conducted by the researcher participating in the study. The transcribed interviews will be anonymised and kept in an office of the Clinical Research Unit Paris Centre in order to carry out the analysis as the interviews are carried out. Following the interview, the participant will be asked to answer the "Preparedness for Caregiving Scale" composed of 8 questions, each evaluated by a 4-level Likert scale. Over a planned inclusion period of 3 months, 75 health professionals (25 doctors, 25 nurses, 25 physiotherapists) will be included. The evaluation criteria of the study will be: i) The diversity of themes extracted during the analysis of the interviews, leading after analysis to a set of meta-themes describing all the experience stories ii) The score on 24 of the "Preparedness for Caregiving Scale".

This study will allow an enrichment of knowledge about the impact of the health crisis on professional and personal life and the difficulties encountered by urban health professionals (doctors, nurses and physiotherapists). But also the identification of the key needs of self-employed health professionals in the management of a health crisis, both in terms of health care skills and in terms of organisation and communication between the various players. Finally, this study will make it possible to identify the traumas experienced and/or felt by self-employed health professionals and the possible consequences of these traumas.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Observational

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
62

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

  • France
      • Paris, France, 75014
        • URC/CIC Paris Centre

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

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

The population of healthcare workers will be selected through Territorial Professional Health Communities (TPHC). These TPHC are organizations designed around a health project and formed on the initiative of city health professionals based on a territory defined by the professionals themselves.

Description

Inclusion Criteria:

  • Communities Health professionals (doctors, nurses, physiotherapist)
  • Be integrate to a Territorial Professional Health Communities (TPHC)
  • Having managed patients during the COVID-19 epidemic

Exclusion Criteria:

  • Health professionals working in the hospital sector
  • Health Students (medical, nursing, physiotherapy)

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

Cohorts and Interventions

Group / Cohort

Group / Cohort

A group or subgroup of participants in an observational study that is assessed for biomedical or health outcomes.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Healthcare professional
Communities Health professionals (doctors, nurses, physiotherapist) Working in the city, In metropolitan France, Having managed patients with COVID-19
Behavioral: Semi-directive interview
Semi-directive interview, lasting a maximum of 45 minutes
Behavioral: Questionnaire : Preparedness for Caregiving Scale
Preparedness for Caregiving Scale - 8 questions

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Diversity of themes extracted about care situations management of the COVID-19 epidemic.
Time Frame: 1 Day
The greatest possible diversity of themes extracted during the analysis of interviews. Identifying the impact of the epidemic of healthcare worker, their personal life and the difficulties they had experienced
1 Day

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Preparedness for caregiving scale (PCS)
Time Frame: 1 Day
8 questions, each evaluated by a 4-level Likert scale (min 0; max 32) higher scores mean better outcome
1 Day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Assistance Publique - Hôpitaux de Paris

Collaborators

Collaborators

An organization other than the sponsor that provides support for a clinical study. This support may include activities related to funding, design, implementation, data analysis, or reporting.
URC-CIC Paris Descartes Necker Cochin

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Director: Flora DEVOS, Nurse MSC PhD, APHP

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)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
September 17, 2020

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
January 12, 2021

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
January 12, 2021

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
November 10, 2020

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 10, 2020

First Posted (Actual)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
November 12, 2020

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
March 31, 2026

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
March 26, 2026

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
March 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • APHP200512

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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