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Multitasking BehaviorMultiCPR2NCT06986226

MultiCPR: The Influence of Ventilations on Mental Arithmetics

A study testing Dose Calculations and Ventilations in people with Multitasking Behavior, run by Medical University of Vienna at 1 site in Austria.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Multitasking Behavior
What is being tested?
Dose Calculations and Ventilations
Could I receive a placebo?
No, everyone receives an active treatment
How many people
38 participants
Where
1 siteAustria
Study dates
7 Jul 2025to 26 Nov 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • Pregnant probands

Trial locations and contacts

1 site in 1 country.

Austria1 site
  • Academic Simulation Center

    Vienna, 1210

Other trials in Austria

About this study

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.

Read more

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.

Being tested
Dose Calculations, Ventilations
Medical subject headings
Multitasking Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dose CalculationsBehavioural

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

  • VentilationsProcedure or surgery

    Performing ventilations during CPR in a 15:2 manner

Study groups in NCT06986226
Study groupRoleWhat they receive
Ventilations/CPRActive comparatorCalculations made with/without performing ventilations - cross over design to decide what to do first, NASA-TLX will be measured
Receives: Behavioral: Dose Calculations; Procedure: Ventilations
no ventilations/CPRActive comparatorCalculations made with/without performing ventilations - cross over design to decide what to do first, NASA-TLX will be measured
Receives: Behavioral: Dose Calculations

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Dose calculations

    Number of correct calculations

    Measured: during 2x2 minutes of inclusion

Secondary outcomes (1)
  1. NASA-TLX

    Nasa Task load index (min: 0, max: 120, higher scores mean higher cognitive load)

    Measured: 4 minutes, 2 times in total per participant

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 May 2025
  2. Study start7 Jul 2025
  3. Primary completion26 Nov 2025
  4. Study completion26 Nov 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
38 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06986226
Sponsor's protocol ID
MultiCPR_2
Acronym
MultiCPR2
Status last verified
Dec 2025
First submitted
29 Apr 2025
Last updated
2 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Dose Calculations and Ventilations in people with Multitasking Behavior, run by Medical University of Vienna at 1 site in Austria.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Dose calculations (time frame: during 2x2 minutes of inclusion). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jan 2026.

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