The Effect of Hybrid Simulation on Evaluating Neonatal Jaundice

NCT ID: NCT05677477

Last Updated: 2023-01-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-20

Study Completion Date

2023-03-31

Brief Summary

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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.

Detailed Description

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Conditions

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Nursing Education

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants
Single blind

Study Groups

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Intervention/Treatment

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

Group Type EXPERIMENTAL

simulation training

Intervention Type OTHER

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

Control

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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simulation training

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

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

19 Years

Maximum Eligible Age

27 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Çankırı Karatekin University

OTHER

Sponsor Role lead

Responsible Party

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Aylin PEKYİGİT

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Müjgan Onarıcı

Role: STUDY_CHAIR

Çankırı Karatekin University

Tuğba Yıldırım

Role: STUDY_CHAIR

Çankırı Karatekin University

Locations

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Çankırı Karatekin Üniversitesi

Çankiri, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Aylin Pekyiğit

Role: CONTACT

05396506489

Facility Contacts

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Aylin Pekyiğit

Role: primary

05413528050

References

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Choi YJ. Exploring experiences of psychiatric nursing simulations using standardized patients for undergraduate students. Asian Nurs Res (Korean Soc Nurs Sci). 2012 Sep;6(3):91-5. doi: 10.1016/j.anr.2012.07.001. Epub 2012 Jul 20.

Reference Type BACKGROUND
PMID: 25030974 (View on PubMed)

Other Identifiers

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CKU

Identifier Type: -

Identifier Source: org_study_id

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