Simulator Use in Newborn First Care

NCT ID: NCT06406738

Last Updated: 2024-07-09

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

COMPLETED

Clinical Phase

NA

Total Enrollment

66 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-15

Study Completion Date

2024-06-30

Brief Summary

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The aim of this study is to determine the effects of using high-fidelity simulators in newborn first care training on the knowledge, skills, satisfaction and self-confidence of midwifery students.

Detailed Description

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Hypotheses H01: There will no difference between the students' knowledge skills, satisfaction, and self-confidence of the simulation-based newborn first care training group and the knowledge skills, satisfaction, and self-confidence score of control group.

The study will be carried out in two different groups. The practice will start with meeting the students who apply to the study. After the students are evaluated in terms of eligibility criteria for the research, the students who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.

Newborn first care training will be given by the responsible investigator, and then one of the groups separated by randomization will perform newborn first care on the second group model using High Reality Simulator. These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.

Conditions

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Newborn; Vitality

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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High Reality Simulator

Newborn first-care training will be given by the responsible investigator, and then one of the groups will be allocated by randomization. Using High Reality Simulator will perform Newborn first-care. These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.

Group Type EXPERIMENTAL

Using High Reality Simulator

Intervention Type OTHER

Using High Reality Simulator will perform newborn first-care.

control group

Using model will perform Newborn first-care. These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Using High Reality Simulator

Using High Reality Simulator will perform newborn first-care.

Intervention Type OTHER

Other Intervention Names

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model

Eligibility Criteria

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Inclusion Criteria

* Agreeing to participate in the research and obtaining written permission,

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Ondokuz Mayıs University

OTHER

Sponsor Role lead

Responsible Party

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Sümeyye BAL

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sumeyye BAL, Ph.D.

Role: STUDY_DIRECTOR

Ondokuz Mayıs University

Locations

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Sumeyye

Ilkadim, Samsun, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2023/3

Identifier Type: -

Identifier Source: org_study_id

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