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CompletedNCT00884559Updated Aug 27, 2012

Leadership Instructions Improve Cardiopulmonary Resuscitation in a High Fidelity Simulation

An interventional study of instruction in Cardiopulmonary Resuscitations, sponsored by University Hospital, Basel, Switzerland. Completed at 1 site in Switzerland. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-08-27.

Sponsored by University Hospital, Basel, Switzerland · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
237
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

Whether teaching leadership with a short debriefing has a positive influence on the performance of cardiopulmonary resuscitation remains largely unknown. The investigators will assess the sustained efficacy of a short leadership debriefing compared to a technical debriefing in a high fidelity simulated cardiopulmonary resuscitation.

Read the detailed description

Context:

Whether the performance of cardiopulmonary resuscitation can be positively influenced by teaching leadership with a short debriefing remains largely unknown

Objective:

To test the hypothesis that (1) leadership instruction are effective and (2) improved leadership results in better performance in a high fidelity simulated cardiopulmonary resuscitation.

Design:

Prospective, randomized-controlled superiority trial

Setting:

Simulator Center of the University Hospital Basel in Switzerland

Patients or Other Participants:

237 volunteer medical students in teams of 3

Intervention:

During a baseline visit, the medical students participate in a video-taped simulated witnessed cardiac arrest. Participants are randomized to receive thereafter a short video-assisted debriefing focusing either on correct positions of arms and shoulders (technical debriefing) or on leadership and communication to enhance team coordination (leadership debriefing). A follow-up simulation is conducted after 4 months. Leadership utterances, technical skills and the resuscitation performance of the teams are compared based on videotapes coded by two independent researchers.

Main Outcome Measures:

The primary outcomes for this study are the amount of hands-on time in the first 180 seconds after the onset of the cardiac arrest and the time elapsed until cardiopulmonary resuscitation was started. Secondary endpoints are the effectiveness of the technical and leadership instructions, respectively.

02

Conditions studied

  • Cardiopulmonary Resuscitations

Keywords

  • Leadership
  • Team building
  • Resuscitation
03

In context

Lead sponsor

University Hospital, Basel, Switzerland is the lead sponsor of 968 studies on the registry; 191 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • volunteer medical students

Exclusion criteria

Exclusion Criteria:

  • no informed consent
05

Study design

Phase
Not applicable
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
237 participants (actual)

Study arms

  • Active comparator
    Technical

    Technical Instructions

    Other: instruction

  • Experimental
    Leadership

    Leadership-Instructions

    Other: instruction

Interventions

  • Otherinstruction

    Debriefing

06

What researchers measure

Primary outcomes

  1. Hands-on time in the first 180 seconds after the onset of the cardiac arrest and the time elapsed until cardiopulmonary resuscitation is started.

    Time frame: 180 sec after start of CPR

Secondary outcomes

  1. The effectiveness of the technical and leadership instructions

    Time frame: 180 sec after starting CPR

07

Study locations

1 site
  • University Hospital Basel
    Basel, Switzerland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 27, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00884559
Lead sponsor
University Hospital, Basel, Switzerland
Responsible party
Sponsor
First posted
Apr 20, 2009
Start date
Nov 2005
Primary completion
Apr 2009
Completion
Apr 2009
Last update
Aug 27, 2012

Study contacts

Sabina Hunziker, MD
principal investigator · University Hospital, Basel, Switzerland
Stephan Marsch, Prof
study chair · Intensive Care unit, University Hospital Basel, Switzerland

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2012. You cannot join it, but the record below documents what was studied.

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