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3D OLV Training Intervention for Pediatric Anesthesia Trainees

A Prospective Randomised Control Trial of Competency Metrics and Educational Interventions in the Learning of One Lung Ventilation Techniques in Children Using Low-cost 3D Printed Tracheo-bronchial Models Among Pediatric Anesthesia Trainees

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03929315
Enrollment
0
Registered
2019-04-26
Start date
2023-04-05
Completion date
2023-04-05
Last updated
2023-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

Keywords

one lung ventilation

Brief summary

One lung ventilation (OLV) in neonates and children is an advanced skill that is necessary for delivery of safe and quality anesthetic care. The current model of training for OLV in the paediatric patient is composed of the apprenticeship model. Trainees learn the techniques of doing the procedure when they encounter a case that allows for it. The model of training is often inadequate for mastery of skills such as OLV as children in this population often have severe debilitating disease often requiring the most experienced anesthesiologist to perform OLV. This limits the training exposure of anesthesia trainees.

Detailed description

Each participant will be subjected to three learning sessions on a 6 year old tracheo-bronchial model. Learning will either be spaced (1 week between learning/testing sessions) or non-spaced (30 minutes between learning/testing sessions). They will have 20 minutes to practice on this model before they are asked to perform the OLV on a younger tracheo-bronchial model (2 yrs, 3 months, 6 weeks). After each testing session, the participants will be provided with feedback. After all learning/testing sessions take place, the participants will be asked to complete a retention test on the 6 week old model six weeks after their last session.

Interventions

BEHAVIORALOLV technique on tracheo-bronchial model

Models will range in size from 6 yrs to 6 weeks.

Sponsors

Clyde Matava
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Pediatric residents and fellows from the Hospital for Sick Children, Toronto

Exclusion criteria

* Refusal to participate in study * Previous experience with at most two OLV in children * Previous experience with at most two OLV in manikins

Design outcomes

Primary

MeasureTime frameDescription
TimeDay 1, after each learning sessionSeconds it took for correct placement of OLV

Secondary

MeasureTime frameDescription
AttemptsWeek 6 or 9Number of attempts per procedure
Wrong entryWeek 6 or 9Number of entries into wrong bronchus
Red-outsWeek 6 or 9Number of red-outs
Overall rating of performanceWeek 6 or 9Measured using Visual Analogue Scale, on a scale of 0-100 where 0=novice and 100=expert
Qualitative endoscopic assessmentWeek 6 or 9Measured using Global Rating Scale of Fibreoptic Bronchoscope Manipulation, on a scale of 4-20, where 4=novice and 20=expert
Satisfaction with task loadDay 1 or Weeks 1-3Measured using Task Load Index, on a scale of 0-100, where 0=very low and 100=very high
Satisfaction with usabilityDay 1 or Weeks 1-3Measured using System Usability Scale, on a scale of 5-50
Wall collisionsWeek 6 or 9Number of wall collisions

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026