- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04432922
Perceptions, Representations and Experiences of Septic Isolation of Hospitalized Patients for COVID-19 Infection
Perceptions, Representations and Experiences of Septic Isolation of Hospitalized
The aim of this study is to analyze the perceptions, representations and experiences of septic isolation of patients hospitalized for COVID-19 infection.
This analysis could lead to better understanding and communication between the medical profession and patients in septic isolation in hospital. It would also provide patient-specific responses to their expectations, as to their families.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
SARS-Cov2 is a new virus responsible for the COVID-19 pandemic. For the first time, it was observed in Wuhan, China in December 2019. For this previously unknown contagious disease, which can cause severe respiratory infections, isolation precautions in hospitals and public places are one of the cornerstones for fighting this pandemic.
Hospital isolation precautions have been present since the 19th century as a means to control the spread of infections. Septic isolation includes contact isolation, droplets and air. Isolation precautions must be prescribed by a physician. To our knowledge, there are few studies about the impact of septic isolation on hospitalized patients at both the psychological level and the relationship with doctors.
This study could enable a better understanding and communication between the medical profession and patients in septic isolation during hospitalization. It could also provide patient-specific responses to their expectations.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Villeneuve St Georges, France, 94190
- Centre Hospitalier Intercommunal de Villeneuve St Georges
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Major patients
- Living in metropolitan France during the SARS-CoV2 pandemic
- Being or having been hospitalized in isolation contact and droplet for a COVID-19 infection (proven or suspected)
- Being in the process of leaving hospital
- Ready for No Opposition for Participation in the Protocol
Exclusion Criteria:
- Patients under guardianship or curatorship
- Patients unable to give free and informed consent;
- Patients under safeguarding justice
- Hospitalized patients on oxygen therapy with speech dyspnea
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
To highlight the perceptions, representations and experiences of septic isolation of patients hospitalized for COVID-19 infection
Time Frame: 1 day
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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to identify key elements to improve the medical discourse on septic isolation among patients
Time Frame: 1 day
|
1 day
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ISOCOV
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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