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Clinical Trials/NCT06869642
NCT06869642CompletedNot Applicable

MultiCPR: The Influence of Chest Compressions on Mental Arithmetics

Medical University of Vienna1 site in 1 country38 target enrollmentStarted: February 10, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
38
Locations
1
Primary Endpoint
PASAT Test

Study Overview

Brief Summary

The purpose of this clinical study is to investigate how performing chest compressions affects the ability to perform mental tasks. In particular, the effect on the participant's ability to perform mental arithmetic will be investigated. The aim is to draw conclusions about the effects of chest compressions on other mental tasks.

2 How does the clinical trial work? This clinical trial will be conducted in several locations and will involve a total of approximately 76 people in two sub-studies (38 people each). The study will be conducted by the Department of Anesthesiology of the Medical University of Vienna.

Participation in this clinical study is expected to last 30 minutes.

The following measures will be carried out exclusively for study reasons:

Depending on the sub-study you are participating in, different tasks will be performed:

Adult sub-study:

During this study, participants will be asked to perform mental arithmetic: Participants will be read a number every 2 seconds and have to add the last two in each case. The numbers are predetermined and randomly generated. At the end, we will evaluate how many results were correct.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Healthy medical professionals trained in CPR (paramedics, prehospital emergency physicians, anesthesiologists, internal medicine doctors, nurses, midwifery students)
  • •CPR Training in the last four years
  • •Fit and rested.

Exclusion Criteria

  • •Pregnant probands

Arms & Interventions

no chest compression

Active Comparator

Calculations made with/without doing chest compressions - cross over design to decide what to do first, NASA-TLX will be measured

Intervention: Doing Pasat-Test (Behavioral)

Chest compression

Active Comparator

Calculations made with/without doing chest compressions - cross over design to decide what to do first, NASA-TLX will be measured

Intervention: Doing Pasat-Test (Behavioral)

Chest compression

Active Comparator

Calculations made with/without doing chest compressions - cross over design to decide what to do first, NASA-TLX will be measured

Intervention: Chest compressions (Procedure)

Outcomes

Primary Outcomes

PASAT Test

Time Frame: during the test, 2 minutes each

Score of PAST Test

Secondary Outcomes

  • Depth of chest compressions(during the pasat test, approx. 3 minutes in total)
  • Frequency of chest compressions(during the pasat test, approx. 3 minutes in total)
  • Leaning of chest compressions(during the pasat test, approx. 3 minutes in total)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mathias Maleczek

Principal Investigator

Medical University of Vienna

Study Sites (1)

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