Mobile Augmented Reality Learning On Insulin Administration Knowledge And Skills Of Patients

NCT ID: NCT07087496

Last Updated: 2025-07-28

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

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-01

Study Completion Date

2024-12-31

Brief Summary

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The goal of this study to determine the effectiveness of insulin administration with augmented reality on increasing the knowledge and skills of patients newly diagnosed with type 2 diabetes on insulin administrations, determining patients' satisfaction with education and comparing the following two strategies: education with the Mobile Augmented Reality and education with the brochure.

* Is Mobile augmented reality application effective on the knowledge scores and insulin application skills of patients with type 2 diabetes on insulin applications?
* Does training with a mobile augmented reality application affect patients' satisfaction with patient education?
* Other patients with type 2 diabetes were given insulin administration training with a brochure prepared by the researcher. All patients who participated in the study were evaluated for insulin administration knowledge and skills after the training.

Detailed Description

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The study was aimed at determining the effectiveness of insulin administration with augmented reality on increasing the knowledge and skills of patients newly diagnosed with type 2 diabetes on insulin administrations, determining patients' satisfaction with education and comparing the following two strategies: education with the Mobile Augmented Reality and education with the brochure.

Methods: The study was conducted between November 1, 2023 and December 31, 2024 with patients newly diagnosed with type 2 diabetes who volunteered to participate in the study and were hospitalized in the first and second wards of the Internal Medicine Department of a state hospital (n=100).

In this quasi-experimental study with the pre-test and post-test design, the participants were allocated into two groups. While the participants in The Intervention Group 1 were given education on insulin administration with a brochure in line with the literature, the participants in the Intervention Group 2 were given education with "Mobile Augmented Reality (MAR)".

The data were collected using the "Individual Information Form", "Knowledge Test", "Scale for Satisfaction with Patient Education", and "Insulin Administration Skill Assessment Checklist".

Conditions

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Diabete Type 2 Augmented Reality Patient Education Patient Education Materials

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The study is a quasi-experimental study with a pre-test and post-test design.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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The Intervention Group 1

The Intervention Group 1 were given education on insulin administration with a brochure

Group Type EXPERIMENTAL

insulin administration training with brochure

Intervention Type OTHER

The Intervention Group 1 (Brochure group): Before the training, the participants were informed about the study, and their written consent was obtained.

Before insulin administration training, a knowledge test was given as a pre-test to determine the participants' knowledge levels on insulin administrations. After the pre-test, a 15-20 minute practical training was given using the brochure prepared for insulin administrations. Immediately after the training, the knowledge test and Scale for Satisfaction with Patient Education were administered as a post-test. After the post-test, the participants were asked to self-administer insulin. The insulin administration skills of the patients were assessed by the researcher using the Insulin Administration Skill Assessment Checklist. After the assessment, the participants were informed about their deficiencies, or incorrect performances.

Intervention Group 2

Intervention Group 2 were given education with "Mobile Augmented Reality (MAR)

Group Type EXPERIMENTAL

Insulin application training with mobile augmented reality

Intervention Type OTHER

Intervention Group 2 (MAR group): Before the training, the participants were briefly informed about how the application would be performed, and their written consent was obtained. Before the insulin administration training was started, the MAR program was shown to them on the tablet by the researcher and the process steps containing QR codes prepared for insulin administration were provided on a blue flat surface and information was given about the use of the application, and a pre-test was administered to determine their knowledge levels on insulin administration. Then, the education application program prepared for insulin administration was opened and the patients were allowed to use it. The training application was performed 20-25 times. Then the post-test was administered to the participants immediately after the training. At the post-test, they were administered the Knowledge Test and Scale for Satisfaction with Patient Education.

Interventions

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Insulin application training with mobile augmented reality

Intervention Group 2 (MAR group): Before the training, the participants were briefly informed about how the application would be performed, and their written consent was obtained. Before the insulin administration training was started, the MAR program was shown to them on the tablet by the researcher and the process steps containing QR codes prepared for insulin administration were provided on a blue flat surface and information was given about the use of the application, and a pre-test was administered to determine their knowledge levels on insulin administration. Then, the education application program prepared for insulin administration was opened and the patients were allowed to use it. The training application was performed 20-25 times. Then the post-test was administered to the participants immediately after the training. At the post-test, they were administered the Knowledge Test and Scale for Satisfaction with Patient Education.

Intervention Type OTHER

insulin administration training with brochure

The Intervention Group 1 (Brochure group): Before the training, the participants were informed about the study, and their written consent was obtained.

Before insulin administration training, a knowledge test was given as a pre-test to determine the participants' knowledge levels on insulin administrations. After the pre-test, a 15-20 minute practical training was given using the brochure prepared for insulin administrations. Immediately after the training, the knowledge test and Scale for Satisfaction with Patient Education were administered as a post-test. After the post-test, the participants were asked to self-administer insulin. The insulin administration skills of the patients were assessed by the researcher using the Insulin Administration Skill Assessment Checklist. After the assessment, the participants were informed about their deficiencies, or incorrect performances.

Intervention Type OTHER

Other Intervention Names

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Interventation group 2

Eligibility Criteria

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Inclusion Criteria

* Being newly diagnosed with Type 2 diabetes at Izmir Bakırçay University Çiğli Training and Research Hospital,
* Not having received diabetes training,
* Not knowing the insulin application,
* Not having used augmented reality before,
* Being 18 years of age or older,
* Being able to use a smartphone.

Exclusion Criteria

* To be diagnosed with Type 2 diabetes at Izmir Bakırçay University Çiğli Training and Research Hospital,
* To have received diabetes education,
* To be familiar with insulin application, -To have used augmented reality before,-
* To be under the age of 18
* To be unable to use a smartphone.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Izmir Bakircay University

OTHER

Sponsor Role lead

Responsible Party

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Hale SEZER

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Abdulkadir Gül, Master

Role: PRINCIPAL_INVESTIGATOR

Izmir Bakırçay University Internal Medicine Nursing

Hale Sezer, PhD

Role: STUDY_DIRECTOR

Izmir Bakırçay University Faculty of Health Science

Locations

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İzmir Bakırçay University Çiğli Education and Research Hospital

Izmir, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Related Links

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Other Identifiers

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Izmir Bakırçay University

Identifier Type: OTHER

Identifier Source: secondary_id

IZBU-HEM-HS-1

Identifier Type: -

Identifier Source: org_study_id

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