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The Effect of Hybrid Simulation on Evaluating Neonatal Jaundice

NCT05677477 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2023-01-10

No results posted yet for this study

Summary

This study will be conducted as a single-blind randomized control group intervention trial to determine the effectiveness of the hybrid simulation method using standard patient and low-fidelity baby simulators in the intervention of nursing students for neonatal physiologic jaundice.

Conditions

  • Nursing Education

Interventions

OTHER

simulation training

A mother scenario with a baby with physiological jaundice will be implemented with the intervention group.

Sponsors & Collaborators

  • Çankırı Karatekin University

    lead OTHER

Principal Investigators

  • Müjgan Onarıcı · Çankırı Karatekin University

  • Tuğba Yıldırım · Çankırı Karatekin University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
27 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-12-20
Primary Completion
2022-12-20
Completion
2023-03-31

Countries

  • Turkey (Türkiye)

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05677477 on ClinicalTrials.gov