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

Sponsor
University Ghent (Other)
Overall Status
Completed
CT.gov ID
NCT05623631
Collaborator
(none)
29
1
1
6
4.8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Survey
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
29 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Delphi Study to Identif Crucial Steps and Errors in the Placement of Chest Tubes
Actual Study Start Date :
Mar 30, 2021
Actual Primary Completion Date :
Sep 28, 2021
Actual Study Completion Date :
Sep 28, 2021

Arms and Interventions

Arm Intervention/Treatment
Other: Delphi study

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.

Other: Survey
Surveys were distributed using REDCap, and participants were asked to complete these within 5 weeks of receiving the invitation.

Outcome Measures

Primary Outcome Measures

  1. Steps and errors presented in round 1 [one year]

    The number of experts who propose a certain step or error

  2. Number of steps and errors passing round 2 [one year]

    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).

  3. Inclusion of steps with their descriptive anchors [one year]

    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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ghent University Hospital Ghent Oost-Vlaanderen Belgium 9000

Sponsors and Collaborators

  • University Ghent

Investigators

  • Principal Investigator: Wouter Willaert, Prof, Dr., University Ghent

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Ghent
ClinicalTrials.gov Identifier:
NCT05623631
Other Study ID Numbers:
  • BC-09710
First Posted:
Nov 21, 2022
Last Update Posted:
Nov 21, 2022
Last Verified:
Nov 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Ghent
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 21, 2022