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Delphi Study to Identify Crucial Steps and Errors in the Placement of Chest Tubes

Primary Purpose

Thoracic Injury

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Survey
Sponsored by
University Ghent
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Thoracic Injury focused on measuring Assessment, Chest Tube Insertion, Rating Scale

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Must be experts in their respective fields. Must hold a degree of Master in Medicine Must have finished the residency training specific to their field (be an attending physician) Must have 5 years post-residency experience Must have performed at least 50 CTIs independently in their career Must have an interest in educating and guiding junior residents in their training. Exclusion Criteria: Insufficient experience in CTI Insufficient experience as an attending physician

Sites / Locations

  • Ghent University Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Delphi study

Arm Description

Participants were asked to complete three rounds of surveys. These surveys collected information on which steps and errors can occur during CTI, and which of these should be included in an assessment tool.

Outcomes

Primary Outcome Measures

Steps and errors presented in round 1
The number of experts who propose a certain step or error
Number of steps and errors passing round 2
The number of experts who agree on the inclusion of each step or error in the assessment tool on a 5-point Likert scale (Strongly disagree - Disagree - Neutral - Agree - Strongly Agree).
Inclusion of steps with their descriptive anchors
The number of experts who agree on the inclusion of each step with their descriptive anchors in the assessment tool on a 5-point Likert scale (Strongly disagree - Disagree - Neutral - Agree - Strongly Agree).

Secondary Outcome Measures

Full Information

First Posted
November 8, 2022
Last Updated
November 18, 2022
Sponsor
University Ghent
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1. Study Identification

Unique Protocol Identification Number
NCT05623631
Brief Title
Delphi Study to Identify Crucial Steps and Errors in the Placement of Chest Tubes
Official Title
Delphi Study to Identif Crucial Steps and Errors in the Placement of Chest Tubes
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
March 30, 2021 (Actual)
Primary Completion Date
September 28, 2021 (Actual)
Study Completion Date
September 28, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Ghent

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this Delphi study is to identify the crucial steps and the errors in Chest Tube Insertion (CTI). These steps and errors will be used for the development of a new assessment tool based on international consensus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thoracic Injury
Keywords
Assessment, Chest Tube Insertion, Rating Scale

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Delphi study
Arm Type
Other
Arm Description
Participants were asked to complete three rounds of surveys. These surveys collected information on which steps and errors can occur during CTI, and which of these should be included in an assessment tool.
Intervention Type
Other
Intervention Name(s)
Survey
Intervention Description
Surveys were distributed using REDCap, and participants were asked to complete these within 5 weeks of receiving the invitation.
Primary Outcome Measure Information:
Title
Steps and errors presented in round 1
Description
The number of experts who propose a certain step or error
Time Frame
one year
Title
Number of steps and errors passing round 2
Description
The number of experts who agree on the inclusion of each step or error in the assessment tool on a 5-point Likert scale (Strongly disagree - Disagree - Neutral - Agree - Strongly Agree).
Time Frame
one year
Title
Inclusion of steps with their descriptive anchors
Description
The number of experts who agree on the inclusion of each step with their descriptive anchors in the assessment tool on a 5-point Likert scale (Strongly disagree - Disagree - Neutral - Agree - Strongly Agree).
Time Frame
one year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Must be experts in their respective fields. Must hold a degree of Master in Medicine Must have finished the residency training specific to their field (be an attending physician) Must have 5 years post-residency experience Must have performed at least 50 CTIs independently in their career Must have an interest in educating and guiding junior residents in their training. Exclusion Criteria: Insufficient experience in CTI Insufficient experience as an attending physician
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wouter Willaert, Prof, Dr.
Organizational Affiliation
University Ghent
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ghent University Hospital
City
Ghent
State/Province
Oost-Vlaanderen
ZIP/Postal Code
9000
Country
Belgium

12. IPD Sharing Statement

Learn more about this trial

Delphi Study to Identify Crucial Steps and Errors in the Placement of Chest Tubes

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