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

NCT ID: NCT04625296

Last Updated: 2021-12-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

62 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-09-17

Study Completion Date

2021-01-12

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Healthcare Worker Facing COVID-19

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Healthcare worker , COVID-19 behaviour

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Healthcare professional

Communities Health professionals (doctors, nurses, physiotherapist) Working in the city, In metropolitan France, Having managed patients with COVID-19

Semi-directive interview

Intervention Type BEHAVIORAL

Semi-directive interview, lasting a maximum of 45 minutes

Questionnaire : Preparedness for Caregiving Scale

Intervention Type BEHAVIORAL

Preparedness for Caregiving Scale - 8 questions

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Semi-directive interview

Semi-directive interview, lasting a maximum of 45 minutes

Intervention Type BEHAVIORAL

Questionnaire : Preparedness for Caregiving Scale

Preparedness for Caregiving Scale - 8 questions

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Flora DEVOS, Nurse MSC PhD

Role: STUDY_DIRECTOR

APHP

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

URC/CIC Paris Centre

Paris, , France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

AP-HP 200512

Identifier Type: -

Identifier Source: org_study_id