None
Conditions
Interventions
VR Group:Participants receive standard endotracheal intubation training while wearing the HoloLens device and using the VR training system to complete one instructional session and one assessment sess
Control group:Participants receive traditional endotracheal intubation training methods.
Sponsors
Shanghai First Maternity and Infant Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1)Medical staff from hospitals across the country who are involved in delivery room resuscitation, including pediatricians, neonatologists, anesthesiologists, obstetricians, nurses, and midwives. 2)No significant visual impairment or dysfunction of the head or hands, and able to operate VR equipment. 3)Voluntarily participate in this study after attending the neonatal resuscitation training course held by our hospital. 4)Pass the theoretical examination on neonatal resuscitation. 5)Participants will be stratified and randomized based on whether they have prior clinical experience in endotracheal intubation.
Exclusion criteria
Exclusion criteria: 1)Presence of head or hand dysfunction that prevents operation of the VR equipment. 2)Inability to tolerate wearing the HoloLens device or experiencing adverse reactions such as dizziness. 3)Already possess advanced endotracheal intubation skills (e.g., neonatal specialists with more than five years of experience).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Standardization of endotracheal intubation performance;Success rate of endotracheal intubation;Procedure time (from preparation to completion of intubation); | — |
Secondary
| Measure | Time frame |
|---|---|
| Difference in participants’ theoretical knowledge before and after training;Basic Psychological Need Satisfaction and Frustration Scale (BPNSFS);NASA Task Load Index (NASA-TLX); | — |
Countries
China
Contacts
Public ContactMing Zhou
Shanghai First Maternity and Infant Hospital
Outcome results
None listed