Skip to content

An Efficacy of Simulator Training for Fiberbronchoscopy in Intensivists

An Efficacy of Simulator Training for Fiberbronchoscopy in Intensivists

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05248347
Enrollment
40
Registered
2022-02-21
Start date
2022-01-01
Completion date
2024-06-30
Last updated
2022-02-21

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

Conditions

Simulator Training

Keywords

Fiberbronchoscopy, Simulation, Assessment, Validity

Brief summary

We evaluated the effects of different fiberbronchoscopy training in how to teach and assess performance. Resident participants with no experience of fiberbronchoscopy, and doctors with little clinical experience with fiberbronchoscopy were eligible for the study.

Detailed description

Participants who passed the theory test were enrolled in the study, and two training simulators for fiberbronchoscopy were used. After randomization, participants were enrolled in Group A (Bronchoscopy training simulator LM-092 )and Group B(The BRONCH Mentor). The test will be taken after practice at the appropriate time.

Interventions

DEVICEBronchoscopy training simulator LM-092 (Koken Co., Ltd, Tokyo, Japan)

Participants who passed the theory test and was enrolled in this group will use this device to practice. After the appropriate time of practice, the test will be taken to evaluate the efficacy.

DEVICEThe BRONCH Mentor (Simbionix, GI-Bronch Mentor, USA)

Participants who passed the theory test and was enrolled in this group will use this device to practice. After the appropriate time of practice, the test will be taken to evaluate the efficacy.

Sponsors

Southeast University, China
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Doctors with little experience of fiberbronchoscopy

Exclusion criteria

* Resident participants who can not complete the study. * Resident participants who can not pass the theroy examination.

Design outcomes

Primary

MeasureTime frameDescription
Final score for examination by Bronchoscopy training simulatorthrough study completion, an average of 3 monthsFinal score of manipulation, orientation, anatomy and actual operation

Secondary

MeasureTime frameDescription
% time at mid-lumen for fiberbronchoscopy manipulation by Bronchoscopy training simulatorthrough study completion, an average of 3 months% time at mid-lumen for fiberbronchoscopy manipulation by Bronchoscopy training simulator
% time at mid-lumenthrough study completion, an average of 3 months% time at mid-lumen
% time at mid-lumen for fiberbronchoscopy manipulationthrough study completion, an average of 3 months% time at mid-lumen for fiberbronchoscopy manipulation
Total wall hits for fiberbronchoscopy manipulation by Bronchoscopy training simulatorthrough study completion, an average of 3 monthsTotal wall hits for fiberbronchoscopy manipulation by Bronchoscopy training simulator

Countries

China

Outcome results

None listed

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