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An Investigation of Trainees' Performance in Augmented Reality Simulation for Invasive Procedure Training

S

Shu-Chen Liao

Status

Completed

Conditions

Healthy

Treatments

Device: AR-US

Study type

Interventional

Funder types

Other

Identifiers

NCT06055400
CGMH AR

Details and patient eligibility

About

The primary aim of this study is to measure the efficacy of augmented reality technology in ultrasound-guided medical intervention.

Full description

BACKGROUND: A significant challenge facing novice physicians is mastering ultrasound(US)-guided procedures, such as central venous catheter (CVC) placement. CVC placements are typically performed on critically ill patients and demand precision and speed. Physicians are often required to switch focus between the ultrasound screen and the patient, memorize multiple images, coordinate hand-eye movements, and interpret 2D images in a 3D context simultaneously. These complexities pose challenges in spatial orientation and impose a considerable cognitive load, affecting both learning and performance. Within the pedagogical landscape, medical educators are exploring the potential merits of Augmented Reality (AR) via head-mounted displays to enhance immersive learning experiences in clinical settings. This study aimed to determine whether AR could ease challenges related to spatial orientation and cognitive overload during this procedure and ultimately enhance skill acquisition for trainees.

Intervention:

Prior to the commencement of the trial, all participants verified their previous training in ultrasound-guided CVC placement. They also provided their written informed consent. The participants are set to be split into two groups as part of a crossover design: the first group will initially be subjected to the traditional ultrasound-guided CVC placement, whereas the second group will begin with the AR-assisted CVC placement

STUDY IMPLICATIONS:

Leveraging AR technology in skill acquisition may reduce trainees' cognitive burden and improve trainee efficiency during ultrasound-guided CVC placement procedures..

Enrollment

47 patients

Sex

All

Ages

20 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  1. Age greater than or equal to 20 years
  2. Final-year medical students (UGY)
  3. Post-year graduate physicians (PGY)
  4. Physicians who have previously received training in ultrasound-guided CVC placement or who have experience with such procedures.

Exclusion Criteria:

Participants who experience discomfort during the process, are pregnant, have high blood pressure, have experienced recent dizziness, have inner ear diseases, suffer from claustrophobia, have undergone recent surgery, have visual impairment, have heart disease, have epilepsy, or refuse to participate.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

47 participants in 2 patient groups

standard US
No Intervention group
Description:
The participants underwent CVC placement using standard ultrasound guidance.
AR-US
Experimental group
Description:
The participants underwent CVC placement using AR-HMD ultrasound guidance.
Treatment:
Device: AR-US

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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