NCT07625072

Brief Summary

Medical staff at the clinic will participate in standard cricothyroidotomy training supplemented with structured mental rehearsal exercises in order to evaluate the usefulness and effectiveness of this approach as a training tool.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
21mo left

Started Jun 2026

Typical duration for not_applicable

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

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Study Timeline

Key milestones and dates

Study Progress8%
Jun 2026May 2028

First Submitted

Initial submission to the registry

May 19, 2026

Completed
16 days until next milestone

First Posted

Study publicly available on registry

June 4, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

June 8, 2026

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2028

Last Updated

June 4, 2026

Status Verified

May 1, 2026

Enrollment Period

1.9 years

First QC Date

May 19, 2026

Last Update Submit

June 1, 2026

Conditions

Keywords

Mental RehearsalMental TrainingeFONA (Emergency Front of Neck Airway)CricothyroidotomyAirway ManagementCritical care

Outcome Measures

Primary Outcomes (1)

  • Objective Structured Clinical Examination (OSCE)

    Participants' procedural performance will be assessed using a standardized Objective Structured Clinical Examination (OSCE). The total score will be expressed as the percentage of correctly performed procedural steps. Scores range from 0% to 100%, with higher scores indicating better procedural performance.

    6 months after enrollment

Secondary Outcomes (2)

  • Procedure completion time

    6 months after entrollment

  • Self-assessed procedural competencies and perceived stress during cricothyroidotomy (individual questionnaire items).

    6 months after enrollment

Study Arms (2)

Routine Training + Mental Rehearsal

EXPERIMENTAL

Participants will undergo standard emergency cricothyrotomy training supplemented with structured mental rehearsal exercises integrated into the routine educational program

Other: Mental Training

Routine Training

NO INTERVENTION

Participants will undergo standard emergency cricothyrotomy training without additional mental rehearsal exercises

Interventions

Structured mental rehearsal exercises integrated into the routine educational program.

Routine Training + Mental Rehearsal

Eligibility Criteria

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

You may qualify if:

  • Medical personnel, including anesthesiology and intensive care specialists, residents, and nursing staff employed within Anesthesiology and Intensive Care Departments of the Medical University of Warsaw network.
  • No prior experience with the use of Mental Rehearsal techniques in performing emergency cricothyroidotomy.
  • Informed consent.

You may not qualify if:

  • Medical personnel involved in the training process of study participants in emergency cricothyroidotomy, including instructors, assisting staff, and examiners.
  • Previous experience with the use of Mental Rehearsal techniques for acquiring competencies in performing emergency cricothyroidotomy.
  • Lack of informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medical University of Warsaw

Warsaw, 02-091, Poland

Location

Study Officials

  • Agata Stężewska, MD

    Medical University of Warsaw

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Agata Stężewska, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 19, 2026

First Posted

June 4, 2026

Study Start

June 8, 2026

Primary Completion (Estimated)

May 1, 2028

Study Completion (Estimated)

May 1, 2028

Last Updated

June 4, 2026

Record last verified: 2026-05

Locations