NCT00884559

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
237

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2005

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2005

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2009

Completed
16 days until next milestone

First Submitted

Initial submission to the registry

April 17, 2009

Completed
3 days until next milestone

First Posted

Study publicly available on registry

April 20, 2009

Completed
Last Updated

August 27, 2012

Status Verified

August 1, 2012

Enrollment Period

3.4 years

First QC Date

April 17, 2009

Last Update Submit

August 24, 2012

Conditions

Keywords

LeadershipTeam buildingResuscitation

Outcome Measures

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.

    180 sec after start of CPR

Secondary Outcomes (1)

  • The effectiveness of the technical and leadership instructions

    180 sec after starting CPR

Study Arms (2)

Technical

ACTIVE COMPARATOR

Technical Instructions

Other: instruction

Leadership

EXPERIMENTAL

Leadership-Instructions

Other: instruction

Interventions

Debriefing

LeadershipTechnical

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • volunteer medical students

You may not qualify if:

  • no informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Basel

Basel, Switzerland

Location

MeSH Terms

Interventions

Educational Status

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Study Officials

  • Sabina Hunziker, MD

    University Hospital, Basel, Switzerland

    PRINCIPAL INVESTIGATOR
  • Stephan Marsch, Prof

    Intensive Care unit, University Hospital Basel, Switzerland

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 17, 2009

First Posted

April 20, 2009

Study Start

November 1, 2005

Primary Completion

April 1, 2009

Study Completion

April 1, 2009

Last Updated

August 27, 2012

Record last verified: 2012-08

Locations