- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04824508
Position of Teamleader and Leadership Performance (LeadPos)
November 14, 2022 updated by: University Hospital, Basel, Switzerland
Effect of the Position of the Teamleader on Quality of Leadership and Team Performance
Investigation in simulated cardiac arrests.
Team leaders are randomly designated.
Designated teamleaders are instructed to lead their team from the position of the patient's head or remote from the patient.
Study Overview
Detailed Description
participants: physicians taking part in voluntary simulator-based workshops.
Teams of 3-4 are formed.
One teammember is randomly allocated as teamleader design: prospective, randomized, single-blind, cross-over intervention: teamleaders are randomized and instructed to lead their team from the conventional position at the patient's head or from a remote hands-off position data analysis: will be performed from videorecordings
Study Type
Interventional
Enrollment (Actual)
151
Phase
- Not Applicable
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
-
-
BS
-
Basel, BS, Switzerland, 4031
- University Hospital
-
-
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
24 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Physicians taking part in voluntary workshops
Exclusion Criteria:
- refusal to participate and/or being videorecorded
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
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Conventional position (head position)
Leaderposition at the patient's head
|
teamleaders are instructed to allocated position
|
|
Active Comparator: Remote position
Leaderposition remote from patient and hands-off
|
teamleaders are instructed to allocated position
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quantity of leadership
Time Frame: 5 minutes
|
Number of leadership utterances made as defined by the adapted Leadership Behaviour Description Questionnaire
|
5 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hands-on time
Time Frame: 5 minutes
|
Hands-on time during the first 5 minutes of the cardiac arrest
|
5 minutes
|
|
Quality of leadership
Time Frame: 5 minutes
|
Type of leadership utterances made as defined by the adapted Leadership Behaviour Description Questionnaire
|
5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Stephan Marsch, University Hospital, Basel, Switzerland
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 1, 2017
Primary Completion (Actual)
June 30, 2022
Study Completion (Actual)
September 30, 2022
Study Registration Dates
First Submitted
March 22, 2021
First Submitted That Met QC Criteria
March 26, 2021
First Posted (Actual)
April 1, 2021
Study Record Updates
Last Update Posted (Actual)
November 15, 2022
Last Update Submitted That Met QC Criteria
November 14, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 4031-Sim
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
Secondary data can be changed Videorecordings of simulations are strictly confidential and cannot be shared
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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