MultiCPR: The Influence of Ventilations on Mental Arithmetics
MultiCPR2
1 other identifier
interventional
38
1 country
1
Brief Summary
The purpose of this clinical study is to investigate how performing ventilations during pediatric resuscitation affects the ability to perform mental tasks. In particular, the effect on the participant's ability to perform dose calculations will be investigated. The aim is to draw conclusions about the effects of ventilations on other mental tasks. How does the clinical trial work? This clinical trial will be conducted in several locations and will involve a total of 38 people. 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 29, 2025
CompletedFirst Posted
Study publicly available on registry
May 22, 2025
CompletedStudy Start
First participant enrolled
July 7, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 26, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 26, 2025
CompletedJanuary 2, 2026
December 1, 2025
5 months
April 29, 2025
December 28, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Dose calculations
Number of correct calculations
during 2x2 minutes of inclusion
Secondary Outcomes (1)
NASA-TLX
4 minutes, 2 times in total per participant
Study Arms (2)
Ventilations/CPR
ACTIVE COMPARATORCalculations made with/without performing ventilations - cross over design to decide what to do first, NASA-TLX will be measured
no ventilations/CPR
ACTIVE COMPARATORCalculations made with/without performing ventilations - cross over design to decide what to do first, NASA-TLX will be measured
Interventions
Dose calculations either with or without performing ventilations during CPR (15:2)
Eligibility Criteria
You may qualify if:
- Healthy medical professionals trained in CPR (paramedics, prehospital emergency physicians, anesthesiologists, internal medicine doctors, nurses, midwifery students, pediatricians)
- CPR Training in the last four years
- Fit and rested.
You may not qualify if:
- \- Pregnant probands
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Academic Simulation Center
Vienna, 1210, Austria
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 29, 2025
First Posted
May 22, 2025
Study Start
July 7, 2025
Primary Completion
November 26, 2025
Study Completion
November 26, 2025
Last Updated
January 2, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share