- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04910243
The Practice of Providing Palliative Care in the Situation of the COVID-19 (Coronavirus Disease 2019) Pandemic in Czech Republic (PEOpLe-C19)
October 14, 2021 updated by: Jan Malaska, Brno University Hospital
The Practice of Providing Palliative Care in the Situation of the COVID-19 (Coronavirus Disease 2019) Pandemic in the Perspective of Physicians and Nurses - Survey Study
Pandemic of coronavirus SARS-CoV-2 (Severe Acute Respiratory Syndrome coronavirus 2) causing the disease COVID-19 (Coronavirus Disease 2019) overwhelmed healthcare and brought new challenges and stressful situations.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In a short time, the capacities of intensive care units (ICU) were filled in many countries and regions.
Due to the need for an excessive number of patients requiring intensive care, physicians and nurses who do not routinely provide care to critically ill patients or do not have the appropriate training (non-ICU clinician) were involved in the care of COVID-19 (Coronavirus Disease 2019) patients.
In this context, ICU directly dedicated to the care of patients with COVID-19 ARDS (Acute Respiratory Distress Syndrome) were also opened.
Non-ICU clinicians were more or less involved together with the standard ICU staff in palliative care, including End-of-Life decision (EOLD) making, even in a situation of limited scarce resources (equipment or personnel).
New workplace and scope of work, which did not correspond to the standard activity or education, most likely led to an increased stress load.
EOLD can also be one of the factors leading to increased stress levels.
The aim of the project is to describe the practice of palliative care for patients with COVID-19 in a situation of pandemic COVID-19 and to identify factors leading to possible moral distress related with EOLD.
Study Type
Observational
Enrollment (Actual)
307
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
-
-
-
Brno, Czechia, 62500
- University Hospital Brno
-
-
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 to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Healthcare providers (physicians and nurses) providing care to patients with COVID-19 admitted at ICU in period of COVID-19 pandemic.
Description
Inclusion Criteria:
- Healthcare providers (physicians and nurses) providing care to patients with COVID-19 admitted at ICU in period of COVID-19 pandemic.
Exclusion Criteria:
- Healthcare professionals who did not managed COVID-19 patients admitted at the ICU in situation of COVID-19 pandemic in the period 2020/2021.
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 |
Intervention / Treatment |
---|---|
Physicians
Physicians managing patients with COVID-19 admitted at ICU during period of COVID-19 pandemic.
|
Physicians providing care to patients with COVID-19 admitted at ICU in period of COVID-19 pandemic will be questioned by electronic web-based survey within Masaryk University information system.
|
Nurses
Nurses providing care to patients with COVID-19 admitted at ICU during period of COVID-19 pandemic.
|
Physicians providing care to patients with COVID-19 admitted at ICU in period of COVID-19 pandemic will be questioned by electronic web-based survey within Masaryk University information system.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of practice of providing palliative care at ICU in COVID-19 pandemic
Time Frame: Through study completion, an average of 1 month
|
Change of practice of providing palliative care including EOLD practice in patients with COVID-19 admitted at ICU during pandemic.
|
Through study completion, an average of 1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Risk factors for moral distress
Time Frame: Through study completion, an average of 1 month
|
Identify factors leading to moral distress during COVID-19 pandemic and describe possible different risk factors by profession
|
Through study completion, an average of 1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Tereza Prokopová, M.D., Masaryk University Brno
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
June 21, 2021
Primary Completion (Actual)
October 14, 2021
Study Completion (Actual)
October 14, 2021
Study Registration Dates
First Submitted
May 28, 2021
First Submitted That Met QC Criteria
June 1, 2021
First Posted (Actual)
June 2, 2021
Study Record Updates
Last Update Posted (Actual)
October 19, 2021
Last Update Submitted That Met QC Criteria
October 14, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PEOpLe-C19 study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.
Clinical Trials on Covid19
-
Anavasi DiagnosticsNot yet recruiting
-
Ain Shams UniversityRecruiting
-
Israel Institute for Biological Research (IIBR)Completed
-
Colgate PalmoliveCompleted
-
Christian von BuchwaldCompleted
-
Luye Pharma Group Ltd.Shandong Boan Biotechnology Co., LtdActive, not recruiting
-
University of ZurichLabor Speiz; Swiss Armed Forces; Universitätsspital ZürichEnrolling by invitation
-
Alexandria UniversityCompleted
Clinical Trials on Questionnaire Survey
-
Centre Hospitalier Universitaire DijonCompleted
-
M.D. Anderson Cancer CenterCompleted
-
Henan University of Traditional Chinese MedicineNot yet recruiting
-
Institut de Sante Parasport Connecte SynergiesFédération Française Handisport (FFH); Université de Montpellier - UMR Santé...RecruitingDisability or Chronic Disease Leading to DisablementFrance
-
Centre Hospitalier Universitaire de NīmesRecruitingCervical Cancer | Transgender Persons | Health Services for Transgender PersonsFrance
-
Brno University HospitalRecruiting
-
M.D. Anderson Cancer CenterActive, not recruitingRectal CancerUnited States
-
Shengjing HospitalActive, not recruitingCareer Burnout | Student BurnoutChina
-
Institut de Sante Parasport Connecte SynergiesAssociation des Paralysees de France (APF)Active, not recruiting
-
Dalarna County Council, SwedenTerminatedOral Leukoplakia | Oral Lichen Planus | ErythroplakiaSweden