NCT06869642

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.

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 Feb 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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 10, 2025

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

February 25, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

March 11, 2025

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2025

Completed
27 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 11, 2025

Completed
Last Updated

May 14, 2025

Status Verified

May 1, 2025

Enrollment Period

1 month

First QC Date

February 25, 2025

Last Update Submit

May 13, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • PASAT Test

    Score of PAST Test

    during the test, 2 minutes each

Secondary Outcomes (3)

  • 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

Study Arms (2)

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

Behavioral: Doing Pasat-TestProcedure: Chest compressions

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

Behavioral: Doing Pasat-Test

Interventions

PASAT-Test either with or without doing chest compressions

Chest compressionno chest compression

Performing chest compressions as desribed in the ERC Guidelines

Chest compression

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)
  • 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, Vienna, 1210, Austria

Location

MeSH Terms

Conditions

Multitasking Behavior

Interventions

Chest Wall Oscillation

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Respiratory TherapyTherapeutics

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

February 25, 2025

First Posted

March 11, 2025

Study Start

February 10, 2025

Primary Completion

March 15, 2025

Study Completion

April 11, 2025

Last Updated

May 14, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations