Menu
Not yet recruiting NCT07228494

Comparative Study of Simulation Technologies for Use in Neonatal Resuscitation Training for Rural Hospitals

No phase Interventional Interprofessional Education Neonatal Resuscitation Rural Health

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: HoloBaby Technology, High Fidelity Simulator Technology.
Who it may be relevant to
Registry conditions: Interprofessional Education, Neonatal Resuscitation, Rural Health. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Conduct a randomized cluster non-inferiority clinical trial with teams of interprofessional neonatal clinicians from rural delivery hospitals. In this trial we will compare HoloBaby, a novel mixed reality simulator technology, to traditional high-technology simulator technology.

Interventions

  • Other HoloBaby Technology
    The intervention will be utilizing HoloBaby technology for Neonatal Resuscitation Simulation Education.
  • Other High Fidelity Simulator Technology
    The intervention will be utilizing HiFi simulator technology for Neonatal Resuscitation Simulation Education.

Primary outcome measures

  • Team-based NRP® Adherence Score [Time frame: 13 months]

Eligibility criteria

Inclusion criteria

  • at least 18 years of age
  • primary clinical role is either physicians, nurses, or respiratory therapists
  • have completed NRP® certification within the two years prior to enrollment
  • attend deliveries at participating hospital in study

Exclusion criteria

\- chronic neck pain, a previous neck injury that requires ongoing precautions, severe motion sickness or vertigo, and/or photosensitive epilepsy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • MaineHealth Maine Medical Center Portland — Portland

Identifiers

NCT: NCT07228494 · 2240996

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗