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Enrolling by invitation NCT05551312

Mobile Virtual Simulation Training in Essential Newborn Care for Healthcare Workers in Low and Middle Income Countries

No phase Interventional Resuscitation

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: Virtual Essential Newborn Care (vENC) training.
Who it may be relevant to
Registry conditions: Resuscitation. Basic parameters: No limits · 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
Nigeria
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Intrapartum asphyxia and prematurity are the leading causes of neonatal mortality in low and middle income countries. Neonatal resuscitation training reduces asphyxia-related newborn mortality and morbidity, but in the absence of continuing low-dose, high frequency practice, these initial gains rapidly decay. The investigators propose to develop and evaluate innovative mobile virtual simulations for refresher training on neonatal resuscitation and essential newborn care to support the retention of knowledge and skills among health care workers in low and middle income countries.

Detailed description

The main goal of this study is to improve newborn mortality and morbidity by using affordable and accessible mobile virtual simulations to provide quality skills training and maintenance for healthcare workers in Low/Middle income countries (LMIC). The investigators hypothesize that mobile devices will provide a readily accessible, standardized alternative to in-person training to maintain skills. This study has the following Specific Aims:

Specific Aim 1: Co-develop and pilot test the usability and efficacy of mobile virtual simulations on early newborn care skills among healthcare workers who attend deliveries in community and health facility-based settings.

Specific Aim 2: Evaluate the impact of the mobile virtual essential newborn care (vENC) training on neonatal resuscitation and care educational indicators and performance outcomes among healthcare workers who provide newborn care in community and health facility-based settings.

Specific Aim 3: Evaluate the impact of virtual simulation refresher training on the rates of neonatal mortality in primary, secondary and tertiary healthcare facilities in Nigeria.

Interventions

  • Other Virtual Essential Newborn Care (vENC) training
    Essential Newborn Care Mobile Virtual Reality Simulation

Primary outcome measures

  • Number of participants with correct performance on essential newborn care objective structured clinical exam (OSCE) items at 6 months [Time frame: at 6 months after in-person training]
  • Early neonatal mortality [Time frame: within 7 days of birth]
Secondary outcome measures (5)
  • Number of participants with correct performance on essential newborn care objective structured clinical exam (OSCE) items by 12 months [Time frame: at 12 months after in-person training]
  • Number of non-breathing newborns receiving bag and mask ventilation [Time frame: at delivery]
  • Number of newborns receiving recommended essential newborn care practices [Time frame: within 7 days of birth]
  • Intrapartum-related mortality [Time frame: on day 1]
  • Early neonatal mortality among babies requiring resuscitation [Time frame: within 7 days of birth]

Eligibility criteria

Inclusion criteria

  • Must have a direct clinical role related to newborn care
  • Is able and willing to attend and complete study-related engagements

Exclusion criteria

  • Healthcare workers who have received essential newborn care course (ENCC) training within the past 12 months at time of recruitment

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
Crossover
Masking
Single blind
Primary purpose
Health services research

Study locations

Nigeria · 1 center
  • University of Lagos — Lagos

Identifiers

NCT: NCT05551312 · STUDY00013179 · 1R21HD107984

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗