The Effect of Hybrid Simulation on Evaluating Neonatal Jaundice

Çankırı Karatekin University

Status: Enrolling

Conditions: Nursing Education

Treatments: Other: simulation training

Study type: Interventional

Funder types: Other

Identifiers

NCT05677477

CKU

Details and patient eligibility

About

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.

Enrollment: 72 estimated patients

Sex: All

Ages: 19 to 27 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Enrolled in the course
• Had not taken this course before
• Accepted to participate in the research

Exclusion criteria

• Have any records of absence
• Taken this course before
• Graduate of health vocational high school

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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72 participants in 2 patient groups

Intervention/Treatment

Experimental group

Description:

In the implementation process of the research, knowledge tests will be applied as pre-test and post-test, and training will be given to the mother who has a baby with physiological jaundice. In the study, the scenario of the mother with a baby with jaundice will be implemented only with the intervention group

Treatment:

Other: simulation training

Control

No Intervention group

Description:

During the application process of the research, knowledge tests will be applied as pre-test and post-test.