The Effect of Augmented Reality Based Training on Preeclampsia Case

NCT06730048 | Not Yet Recruiting

• 1 other identifier: Inonu3
• Study Type: interventional
• Target: 84
• Locations: 1 country
• Sites: 1

Brief Summary

However, no study has been found in the care of preeclampsia, which is highly effective on maternal and fetal health. Therefore, this study was planned to determine the effect of augmented reality-based training on the diagnosis and intervention planning skills of nursing students.

Conditions

Preeclampsia; Nursing Care; Pregnancy; Augmented Reality

Keywords

preeclampsia; nursing care; pregnancy; augmented reality

Outcome Measures

Primary Outcomes (1)

• Preeclampsia Nursing Care Plan

  he nursing care plan consists of 4 open-ended questions including nursing diagnosis, risks, interventions and evaluation. Students will receive 3 points for each correct diagnosis. If they write all of the diagnoses, they will receive a total of 48 points from the diagnoses. If they correctly write 2 of the risk factors related to the diagnosis of preeclampsia added to the diagnoses for each diagnosis, they will receive 1 point from each diagnosis. They will receive a maximum of 16 points from risks. If they write at least 5 nursing interventions for each diagnosis, they will receive 2 points for each diagnosis. A maximum of 32 points will be obtained from interventions. The evaluation part will be 0.25 points. If they write the evaluations of all diagnoses correctly, they will receive 4 points. A total of 100 points can be obtained from the nursing care plan, with a minimum of 0 and a maximum of 48+16+32+32+4.

  one month

Secondary Outcomes (3)

• Participant Information Form

  one month

• Preeclampsia Knowledge Test

  one month

• Presence Scale

  one month

Study Arms (2)

experimental group

EXPERIMENTAL

An appointment will be made to meet with the students in the experimental group in a suitable classroom of the school. After the pre-test data, the students in the experimental group will be shown the preeclampsia case with virtual glasses for about 5-10 minutes. Then the post-test will be applied. A scenario including preeclampsia case and nursing care practices will be created in the virtual reality environment, and 10 experts will be consulted about the scenario before the students are shown it. This application will not have any side effects.

Other: Experimental Group

control group

OTHER

After the pre-test data, the preeclampsia case will be explained to the students in the control group with the classical lecture method in the Women's Health and Diseases Nursing course and the post-test will be applied.

Other: Control group (placebo)

Interventions

Experimental Group OTHER

An appointment will be made to meet with the students in the experimental group in a suitable classroom of the school. After the pre-test data, the students in the experimental group will be shown the preeclampsia case with virtual glasses for about 5-10 minutes. Then the post-test will be applied. A scenario including preeclampsia case and nursing care practices will be created in the virtual reality environment, and 10 experts will be consulted about the scenario before the students are shown it. This application will not have any side effects.

experimental group

Control group (placebo) OTHER

After the pre-test data, the preeclampsia case will be explained to the students in the control group with the classical lecture method in the Women's Health and Diseases Nursing course and the post-test will be applied.

control group

Eligibility Criteria

• Age: 18 Years - 45 Years
• Gender Eligibility Details: Inclusion criteria; * Continuing the course of Women's Health and Diseases Nursing, * Volunteering to participate in the research, * No physical or psychological health problems preventing the completion of the research forms. Exclusion criteria * Not watching the whole case given with virtual glasses, * Failure to attend class during the week of the preeclampsia lecture in the course syllabus.
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Continuing the course of Women's Health and Diseases Nursing,
• Volunteering to participate in the research,
• No physical or psychological health problems preventing the completion of the research forms.

You may not qualify if:

• \- Not watching the whole case given with virtual glasses,
• Failure to attend class during the week of the preeclampsia lecture in the course syllabus.

Sponsors & Collaborators

• Inonu University: lead

Study Sites (1)

Inonu University

Malatya, 44200, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Pre-Eclampsia

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Hypertension, Pregnancy-Induced; Pregnancy Complications; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases

Intervention Hierarchy (Ancestors)

Epidemiologic Research Design; Epidemiologic Methods; Investigative Techniques; Research Design; Methods

Central Study Contacts

simge öztürk, Ph.D

CONTACT

05398751788; sozturk@bartin.edu.tr

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, OUTCOMES ASSESSOR
• Masking Details: experimental group will use augmented reality sension and outcome assessments will be performend by a investigator who was blinded to group allocation.
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Ph.D Student

Model Details: two-group study, experimental and control group

Study Record Dates

• First Submitted: December 8, 2024
• First Posted: December 12, 2024
• Study Start: December 20, 2024
• Primary Completion: February 20, 2025
• Study Completion: August 20, 2025
• Last Updated: December 12, 2024

Record last verified: 2024-12

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)