Effects of the Mobile Application Developed for Families After the Earthquake on First Aid Knowledge and Burn Prevention

November 19, 2024 updated by: Gamze BOZKUL, Tarsus University

Effects of the Mobile Application Developed for Families Living in Tent Cities and Container Houses After the Earthquake on Burn Prevention and First Aid Knowledge and Burn Development

The aim of this project was to determine the effect of the burn prevention and first aid mobile application developed for families living in tent cities and container houses after the earthquake on the burn prevention and first aid knowledge of families and the development of burns in the first two months after the mobile application. The research was planned as a prospective, two-arm (1:1), randomized controlled trial. The study population will consist of families living in tent cities and container houses in Şanlıurfa. As a result of the power analysis performed in the G*Power program, the sample group will consist of 30 families from the tent city and 30 families from the container city, taking into account the losses with a power of 90% and a maximum bidirectional 5% type error. All of the families (30 mobile application-study group; 30 control group) who make up the sample of the research will be given a training (powerpoint presentation) prepared by the researcher in line with the literature, and burn prevention and first aid practices will be explained and their questions will be answered. Then, the training to be given with the mobile application will be downloaded to the phones of the families in the experimental group and the training will continue through the application. In the study, data will be collected with the "Descriptive Characteristics Form", "Information Form on Burn Prevention and First Aid" and "Burn Development Follow-up Form", which include the descriptive information of the families. The data obtained from the study will be analyzed in computer environment.

Study Overview

Detailed Description

The aim of this project was to determine the effect of the burn prevention and first aid mobile application developed for families living in tent cities and container houses after the earthquake on the burn prevention and first aid knowledge of families and the development of burns in the first two months after the mobile application.The research was planned as a prospective, two-arm (1:1), randomized controlled trial. This randomized controlled trial will be reported according to CONSORT guidelines. The research population will consist of families living in tent cities and container houses in Şanlıurfa. As a result of the power analysis performed in the G*Power program, the sample group will consist of 30 families from the tent city and 30 families from the container city, taking into account the losses with a power of 90% and a maximum bidirectional 5% type error. All of the families (30 mobile application-study group; 30 control group) who make up the sample of the research will be given a training (powerpoint presentation) prepared by the researcher in line with the literature, and burn prevention and first aid practices will be explained and their questions will be answered. Then, the training to be given with the mobile application will be downloaded to the phones of the families in the experimental group and the training will continue through the application. Thus, families will be able to access the training from the mobile application at any time after the training. The primary results of the research are the effect of the mobile application on burn prevention and first aid knowledge. The secondary outcome of the study is the effect of the mobile application on the development of burns in the first two months after the mobile application. In the study, data will be collected with the "Descriptive Characteristics Form", "Information Form on Burn Prevention and First Aid" and "Burn Development Follow-up Form", which include the descriptive information of the families. The data obtained from the study will be analyzed in computer environment.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Mersin, Turkey
        • Gamze Bozkul

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Living in a tent-container house after the earthquake,
  • No communication problems in the family,
  • At least one person in the family who will participate in the training can speak Turkish,
  • Written and verbal permission to participate in the study was obtained.

Exclusion Criteria:

  • Not living in a tent-container house after the earthquake,
  • Not wanting to participate in the research,
  • The family wants to separate at any time,
  • Relocation from tent cities or container houses included in the implementation area during the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: EXPERIMENTAL GROUP
All of the families constituting the sample of the study (30 mobile application-study group) will be told about burn prevention and first aid practices with a training (powerpoint presentation) prepared by the executive researcher in line with the literature and their questions will be answered. Then, the training to be given with the mobile application will be downloaded to the phones of the families in the experimental group and the training will continue through the application.

Mobile application: The content of the mobile application that can be used continuously after the presentation in the education of families will consist of three parts.

In the first section: There will be short information notes and visuals on burn diagnosis and types.

Second part: Frequently seen burns as a result of home accidents will be introduced and the precautions to be taken will be included through visuals.

Third Section: First aid applications specific to each type of burn (scalding, fire-flame, hot contact, electrical, chemical) will be presented with visuals and information notes.

Family Information Training: The content of the training to be held for families in the form of a powerpoint presentation is as follows: definition of burns, classification of burns, common causes of burns at home, measures to prevent burns at home, first aid applications in burns.
Sham Comparator: CONTROL GROUP
All of the families constituting the sample of the study (30 control group) will be told about burn prevention and first aid practices with a training (powerpoint presentation) prepared by the executive researcher in line with the literature and their questions will be answered.
Family Information Training: The content of the training to be held for families in the form of a powerpoint presentation is as follows: definition of burns, classification of burns, common causes of burns at home, measures to prevent burns at home, first aid applications in burns.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Burn prevention
Time Frame: 6 months
Information Form on Burn Prevention and First Aid: Questions prepared by the researchers inquiring information about the training (first aid in burns, risky situations for burns, precautions to be taken, etc.).
6 months
First aid knowledge
Time Frame: 6 months
Information Form on Burn Prevention and First Aid: Questions prepared by the researchers inquiring information about the training (first aid in burns, risky situations for burns, precautions to be taken, etc.).
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Burn development status
Time Frame: 2 months
Burn Development Monitoring Form: It is a form that inquires whether burns developed within the first two months after the mobile application, and in case of development, the status of being affected by the burn and the first aid applications made.
2 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gamze Bozkul, Tarsus University
  • Study Director: Sabri Karahan, Harrran University
  • Principal Investigator: Gülay ALTUN UĞRAŞ, Mersin University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2023

Primary Completion (Actual)

March 1, 2024

Study Completion (Actual)

April 1, 2024

Study Registration Dates

First Submitted

November 24, 2023

First Submitted That Met QC Criteria

November 24, 2023

First Posted (Actual)

December 4, 2023

Study Record Updates

Last Update Posted (Estimated)

November 22, 2024

Last Update Submitted That Met QC Criteria

November 19, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • TU-BOZKUL-006

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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