- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05908058
Emotional Changes Between Emergency and Intensive Care Unit and On-site Counter Staffs After COVID-19 Infection (COVID-19)
The Investigation of Emotional Changes Between Emergency and Intensive Care Unit and On-site Counter Staffs After COVID-19 Infection and Exploring The Impact of Personnel Emotional Adjustment About Duty and Future Planning
Study Overview
Status
Intervention / Treatment
Detailed Description
The emotional and work changes of the staffs and on-site counter staffs will have a certain impact during this pandemic period. Because a large number of critically ill patients are obstructive in emergency and critical care unit. It will induce a huge impact on the deployment of medical team manpower The purpose of this study is to understand the situation of emergency and intensive care unit personnel after COVID-19 infection. It will help the hospital superintendent to understand the impact of emotional adjustment on its own work, understand the emotional situation of on-site personnel, future planning and r deployment.
- Explore the emotional changes of on-site emergency department and critical care unit staffs and on-site counter staffs by filling in questionnaires
- Understand the emotional changes of personnel in various units and on-site counter personnel and how to adjust.
- Arrange the Likert scale questionnaire with Meleis Nursing Transitional Theory. The different aspects of the questionnaire to quantify the emotional changes of the emergency and critical unit personnel and the on-site counter personnel. Each questionnaire takes about 20 minutes to 30 minutes to fill this questionnaire.
- Analyze the emotional adjustment of the staffs in the acute and severe unit that affects their own work and how to affect the relationship between colleagues and medical practice execution.
- This study uses empirical evidence to analyze and evaluate the emotional changes of emergency department and intensive care unit personnel and on-site counter personnel, understand the rationality of hospital manpower deployment and make the assistance needed
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Chia-Hsi Chen, Dr
- Phone Number: 3708 886-5-2756000
- Email: urologist3509@gmail.com
Study Locations
-
-
-
Chiayi City, Taiwan, 60069
- Recruiting
- St. Martin De Porres Hospital
-
Contact:
- Chen Chia-Hsi, MD
- Phone Number: 3708 886-5-275600
- Email: urologist3509@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- emergency department and intensive care unit personnel after facing their own infection with COVID-19.
Exclusion Criteria:
- Exclude those who fill in the questionnaire with incomplete information
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Investigation of Emotional Changes between Emergency and Intensive care unit and On-site Counter Staffs after COVID-19 Infection and Exploring The Impact of Personnel Emotional Adjustment about Duty and Future Planning
Time Frame: 2 months
|
There is a huge impact on the deployment of medical team manpower after critically ill patients accumulated in emergency room and critical care unit. The purpose of this study is to understand the emotional change situation of emergency and intensive care unit personnel after covid-19 infection. It will help the superintendent to understand the impact of emotional adjustment on its own work, understand the situation of on-site personnel and adjust manpower planning and deployment. |
2 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Chia-Hsi Chen, Dr, St. Martin De Porres Hospital, Emergency Medicine Department
Publications and helpful links
General Publications
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 23B-003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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