- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06375148
A Questionnaire Survey on Cognition of Enteral Nutrition Implementation in Patients Requiring Mechanical Ventilation in Prone Position
April 16, 2024 updated by: Second Affiliated Hospital, School of Medicine, Zhejiang University
Prone ventilation is an important treatment for respiratory failure with intractable hypoxia, and the Corona Virus Disease 2019(COVID-19 ) outbreak has further elevated the status of prone ventilation.
Early enteral nutrition (EN) is also recognised as an important measure to improve the prognosis of critically ill patients.
However, the administration of enteral nutrition during prone position is still quite controversial.
In this paper, we analysed the tolerance and safety of enteral nutrition in the prone position by reviewing studies before and after the COVID-19 outbreak.
Key strategies to improve the tolerability of enteral nutrition in the prone position are also summarised and discussed.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Detailed Description
We plan to carry out the following research: through multi center investigation and research, to understand the current situation of critical care workers' cognition of enteral nutrition in patients with severe prone position ventilation.
1. research purpose: to understand the current situation of cognition of critically ill medical staff on enteral nutrition in patients with severe prone position ventilation.
2. research design and methods: This study includes three parts: 1. confirmation of the research object; 2. research content and specific content of the questionnaire; 3. statistical analysis of questionnaire results.
Research object: investigation unit: intensive care unit (ICU) of secondary grade A and above comprehensive hospitals (including traditional Chinese medicine and integrated traditional Chinese and Western medicine hospitals), including comprehensive ICU, central ICU, emergency ICU, medical ICU, surgical ICU, brain ICU, and other specialized ICUs.
respondents: medical staff working in the above ICU during the survey.
It does not include resident trainees, interns and other types of personnel who are not in the Department.
Refresher trainees, if their job is ICU medical care, can also fill in the questionnaire, but it should be noted that the unit filling in is the original unit, not the refresher unit.
Research content: Investigation on the current situation of medical staff's understanding of enteral nutrition in patients with severe prone position ventilation: a multicenter investigation.
The questionnaire is divided into three parts (basic information, prone position ventilation information, enteral nutrition).
See the questionnaire for details.
The main purpose is to describe the current situation of critical care physicians' cognition of the implementation of enteral nutrition in prone position requiring mechanical ventilation.
The main outcome measure was whether enteral nutrition had been started before prone position, and whether enteral nutrition would be cut off because of the need for prone position.
Research methods: for the research objects that meet the inclusion criteria, the electronic questionnaire was issued in January 2023 for questionnaire survey, and the electronic questionnaire data were exported in the background in February 2023, and the questionnaire data were sorted out for statistical analysis.
The main ways to issue questionnaires are as follows: 1. issue questionnaires through the quality control center of Zhejiang Province; 2. the questionnaire was distributed through the quality control center of traditional Chinese medicine critical care medicine in Sichuan Province; 3. through the severe nutrition group / nursing group of Zhejiang nutrition branch; 4. the questionnaire was distributed through the critical care medicine branch of the Chinese Research Hospital Association; 5. through the emergency world and emcrit wechat platform; 6. other ways.
Study Type
Observational
Enrollment (Estimated)
200
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
-
-
-
Zhenjiang, China
- The Second Affiliated Hospital of Zhejiang University School of Medicine
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
Medical staff working in the above ICU during the survey.
Description
Inclusion Criteria:
- The intensive care unit (ICU) of the secondary grade A and above general hospitals (including traditional Chinese medicine and integrated traditional Chinese and Western medicine hospitals), including comprehensive ICU, central ICU, emergency ICU, internal medicine ICU, surgical ICU, brain ICU, and other specialized ICUs.
Exclusion Criteria:
- Resident trainees, interns and other types of personnel not in the Department
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 |
|---|---|
|
Zhejiang Quality Control Center
|
prone position ventilation
|
|
Sichuan Provincial Center for quality control of TCM critical care medicine
|
prone position ventilation
|
|
Severe nutrition group / nursing group of Zhejiang nutrition branch
|
prone position ventilation
|
|
Critical care medicine of China Research Hospital Association
|
prone position ventilation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
A questionnaire survey on cognition of enteral nutrition implementation in patients requiring mechanical ventilation in prone position
Time Frame: The questionnaire method was started in April, and the data statistics were completed in June
|
Questionnaires were sent out in April, and data statistics were carried out in June
|
The questionnaire method was started in April, and the data statistics were completed in June
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Libing Jiang, MASTER, Second Affiliated Hospital, School of Medicine, Zhejiang University
- Principal Investigator: Chengfei Wang, MASTER, Second Affiliated Hospital, School of Medicine, Zhejiang University
- Principal Investigator: Shanxiang Xu, MASTER, Second Affiliated Hospital, School of Medicine, Zhejiang University
- Principal Investigator: Yongan Xu, DOCTOR, Second Affiliated Hospital, School of Medicine, Zhejiang University
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)
March 20, 2024
Primary Completion (Estimated)
May 30, 2024
Study Completion (Estimated)
June 30, 2024
Study Registration Dates
First Submitted
April 16, 2024
First Submitted That Met QC Criteria
April 16, 2024
First Posted (Actual)
April 19, 2024
Study Record Updates
Last Update Posted (Actual)
April 19, 2024
Last Update Submitted That Met QC Criteria
April 16, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- Yan2024-0052
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.
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