NCT07615582

Brief Summary

Cognitive failure under multitasking conditions has been demonstrated in various settings, including healthcare. However, in anesthesiology, the impact of multitasking on clinical performance has not yet been fully characterized. The objective of our study is to evaluate the impact of multitasking on anesthesiologists' clinical performance in a simulated setting.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
35

participants targeted

Target at P25-P50 for all trials

Timeline
6mo left

Started Jun 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress8%
Jun 2026Dec 2026

First Submitted

Initial submission to the registry

May 22, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 29, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

June 10, 2026

Status Verified

June 1, 2026

Enrollment Period

6 months

First QC Date

May 22, 2026

Last Update Submit

June 5, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Concordance score with the expert panel on a Script Concordance Test (SCT)

    Each item of the SCT is scored out of 1 point, and the sum of the points, converted to a 100-point scale, defines the percentage of concordance with the expert panel.

    At two time points: - During simulation session under multitasking conditions - During control visit under quiet conditions

Secondary Outcomes (4)

  • Manual ventilation performance assessed by variance of expiratory tidal volume (ml)

    - Training before simulation: baseline - During simulation: ventilation only, ventilation plus clinical questions

  • Manual ventilation performance assessed by variance of respiratory rate (cycles/minute)

    - Training before simulation: baseline - During simulation: ventilation only, ventilation plus clinical questions

  • Cognitive load assessed by the NASA-TLX index (score out of 100)

    A two time points: - Evaluating cognitive load of manual ventilation alone, before simulation after training. - Evaluation cognitive load of multitasking, at the end of the simulation session

  • Time to answer items of the script concordance test (seconds)

    Two time points: intervention and control.

Other Outcomes (3)

  • Exploratory sub-group analysis of the primary outcome measure

    Two time points: intervention and control.

  • Exploratory subgroup analyses of expiratory tidal volume variance and respiratory rate variance

    - Training before simulation: baseline - During simulation: ventilation only, ventilation plus clinical questions

  • Descriptive analysis of ventilation parameters

    Training phase (baseline), simulation phase (ventilation-only and ventilation plus clinical questions)

Interventions

Simulation training session during which participants will be required to multitask by performing manual mask ventilation on a manikin while answering oral clinical questions administered in the form of Script Concordance Tests (SCTs).

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of a sample of anesthesiology and intensive care physicians working at Grenoble University Hospital.

You may qualify if:

  • Anesthesiology and intensive care resident or attending physician
  • Written informed consent

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre d'Évaluation et de Simulation Alpes Recherche (CESAR)

Grenoble, 38700, France

Location

Related Publications (7)

  • Sujka JA, Safcsak K, Bhullar IS, Havron WS 3rd. Simulation-Based Testing of Pager Interruptions During Laparoscopic Cholecystectomy. J Surg Educ. 2018 Sep-Oct;75(5):1351-1356. doi: 10.1016/j.jsurg.2018.01.012. Epub 2018 Feb 1.

    PMID: 29396277BACKGROUND
  • Murji A, Luketic L, Sobel ML, Kulasegaram KM, Leyland N, Posner G. Evaluating the effect of distractions in the operating room on clinical decision-making and patient safety. Surg Endosc. 2016 Oct;30(10):4499-504. doi: 10.1007/s00464-016-4782-4. Epub 2016 Feb 19.

    PMID: 26895919BACKGROUND
  • McCurdie T, Sanderson P, Aitken LM. Traditions of research into interruptions in healthcare: A conceptual review. Int J Nurs Stud. 2017 Jan;66:23-36. doi: 10.1016/j.ijnurstu.2016.11.005. Epub 2016 Nov 10.

    PMID: 27951432BACKGROUND
  • Adams TN, Rho JC. Multitasking simulation: Present application and future directions. Med Teach. 2017 Feb;39(2):120-122. doi: 10.1080/0142159X.2016.1230666. Epub 2016 Sep 15.

    PMID: 27633071BACKGROUND
  • Jackson KM, Shaw TH, Helton WS. Evaluating the dual-task decrement within a simulated environment: Word recall and visual search. Appl Ergon. 2023 Jan;106:103861. doi: 10.1016/j.apergo.2022.103861. Epub 2022 Aug 20.

    PMID: 35998391BACKGROUND
  • Westbrook JI, Woods A, Rob MI, Dunsmuir WT, Day RO. Association of interruptions with an increased risk and severity of medication administration errors. Arch Intern Med. 2010 Apr 26;170(8):683-90. doi: 10.1001/archinternmed.2010.65.

    PMID: 20421552BACKGROUND
  • Gui JL, Nemergut EC, Forkin KT. Distraction in the operating room: A narrative review of environmental and self-initiated distractions and their effect on anesthesia providers. J Clin Anesth. 2021 Feb;68:110110. doi: 10.1016/j.jclinane.2020.110110. Epub 2020 Oct 16.

    PMID: 33075633BACKGROUND

MeSH Terms

Conditions

Multitasking Behavior

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Jean-Noël Evain, MD, PhD

CONTACT

Caroline Sanchez, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 22, 2026

First Posted

May 29, 2026

Study Start

June 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

June 10, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Single center study

Locations