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Task Focusing Strategy During a Simulated Cardiopulmonary Resuscitation

Impact of a Task Focusing Strategy on Perceived Stress Levels and Performance During a Simulated Cardiopulmonary Resuscitation: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01645566
Enrollment
124
Registered
2012-07-20
Start date
2007-12-31
Completion date
2008-07-31
Last updated
2012-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Stress

Keywords

cardiopulmonary resuscitation, stress, intervention

Brief summary

This is a prospective randomized controlled study. The aim of this study is to 1. describe the stress patterns experienced during a CPR situation; 2. investigate whether the perceived stress was associated with CPR performance in terms of hands-on time and time to start CPR; 3. to investigate whether this task focusing strategy reduces perceived stress levels, and 4. whether this translates into better CPR performance. Based on findings that clear, directive leadership can enhance performance in cardiac resuscitation, we further 5) investigate if stress was associated with fewer leadership statements.

Interventions

BEHAVIORALinstruction

instructions about focusing on relevant task elements by posing two task-focusing questions (what is the patient's condition?, what immediate action is needed?) when feeling overwhelmed by stress (intervention-group)

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 4th year medical students

Exclusion criteria

* No informed consent

Design outcomes

Primary

MeasureTime frameDescription
perceived levels of stress and feeling overwhelmed (stress/overload)time from start of CPR until scenario is finished (usually 5-10min)This is a simulator study and the study starts after students entered the simulator and the manikin has a cardiac arrest. The scenarios usually last for not more than 5-10 min at which time point the study is finished

Secondary

MeasureTime frameDescription
hands-on timetime from start of CPR until scenario is finished (usually 5-10min)This is a simulator study and the study starts after students entered the simulator and the manikin has a cardiac arrest. The scenarios usually last for not more than 5-10 min at which time point the study is finished
time to start CPRtime from start of CPR until scenario is finished (usually 5-10min)
Number of leadership statementstime from start of CPR until scenario is finished (usually 5-10min)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 23, 2026