NCT06986226

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

87
On Track

Trial Health Score

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

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 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

First Submitted

Initial submission to the registry

April 29, 2025

Completed
23 days until next milestone

First Posted

Study publicly available on registry

May 22, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

July 7, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 26, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 26, 2025

Completed
Last Updated

January 2, 2026

Status Verified

December 1, 2025

Enrollment Period

5 months

First QC Date

April 29, 2025

Last Update Submit

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 COMPARATOR

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

Behavioral: Dose CalculationsProcedure: Ventilations

no ventilations/CPR

ACTIVE COMPARATOR

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

Behavioral: Dose Calculations

Interventions

Dose calculations either with or without performing ventilations during CPR (15:2)

Ventilations/CPRno ventilations/CPR
VentilationsPROCEDURE

Performing ventilations during CPR in a 15:2 manner

Ventilations/CPR

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Multitasking Behavior

Interventions

Ventilation

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Environment, ControlledEnvironmentEnvironment and Public Health

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

Locations