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Just-In-Time Rapid Cycle Deliberate Practice Simulation Intubation Training Among Novice Pediatric Anesthesia Trainees: A Randomized Control Study

Just-In-Time Rapid Cycle Deliberate Practice Simulation Intubation Training Among Novice Pediatric Anesthesia Trainees: A Randomized Control Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04472195
Enrollment
182
Registered
2020-07-15
Start date
2020-08-01
Completion date
2022-04-30
Last updated
2025-01-15

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

Conditions

Anesthesia

Brief summary

The purpose of this study is to assess the impact of Just-In-Time (J-I-T) Rapid Cycle Deliberate Practice (RCDP) Simulation Training on laryngoscopy competency among novice pediatric anesthesia trainees.

Detailed description

Multiple intubation attempts in infants are potentially more harmful than previously suspected. Emerging literature suggests each additional attempt past an initial laryngoscopy correlates with a two-fold increase in complications. Therefore, striving to secure the neonate/infant airway on the first attempt is optimal for infant safety. Novice trainees lack experience with airway management in small children. To promote a patient safety culture among the multitude of rotating trainees at Boston Children's Hospital the investigators would like to augment airway management with Rapid Cycle Deliberate Practice Simulation Training (RCDP). Rotating trainees at BCH main campus will be prospectively randomized to experimental vs. control group for intubation of neonates and infants less than or equal to 12 months of age. Infants with known congenital heart disease, known or suspected difficult airways, or COVID-19 positive status will be excluded from the study. The experimental group will review a pre-induction airway management plan for their upcoming case and rapid cycle deliberate practice (RCDP) on a simulator with an anesthesia attending coaching on technique prior to real patient intubation. Primary outcome measure will be first attempt success rate. Other outcome measures include: complication rates, a team developed Likert scale that investigates intubation competency and utility of JIT/RCDP training, and NASA-TLX (a validated cognitive task load index). The study would be the first to directly determine how and if simulation-based pediatric airway interventions are immediately transferable to actual clinical environments in pediatric anesthesiology. Such a study may change how training programs prepare novices for game time performance and become a new standard of care in airway management training.

Interventions

OTHERSimulation Airway Coaching

Airway coaching on laryngoscopy technique for intubation of neonates/infants within 1 hour of case utilizing RCDP simulation technique.

Sponsors

Boston Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Non-crossover, Prospective Randomized Controlled Trial

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Anesthesia Residents * SRNA * Pediatric Anesthesia Fellows

Exclusion criteria

* Medical Students * Off-Service Rotators

Design outcomes

Primary

MeasureTime frameDescription
1st attempt success rateThrough study completion, anticipated 12-15 monthsTrainee first attempt success rate will be observed by the study team

Secondary

MeasureTime frameDescription
Complication rateThrough study completion, anticipated 12-15 monthsTrainee complication rates of laryngoscopy will be observed by the study team
Self evaluation of neonate/infant laryngoscopyThrough study completion, anticipated 12-15 monthsTrainees will fill out Likert questions developed in conjunction with Boston Children's Survey Methodologist
Evaluation of utility of JIT/RCDPThrough study completion, anticipated 12-15 monthsTrainees will fill out Likert Questions developed in conjunction with Boston Children's Survey Methodologist
Cognitive Load in intubating patientThrough study completion, anticipated 12-15 monthsNASA-TLX will be administered to trainees to evaluate cognitive task load

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026