A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE

April 14, 2023 updated by: Merve Çakırlı, Eskisehir Osmangazi University

A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE: PILOT STUDY

The study included 2 stages: In the first, a mobile application with content including urotherapy training and patient follow-up was developed. In the second, a pilot study with the developed mobile application was carried out with 10 children.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The study include two stages. In the first, a mobile application was developed that can be used by children with urinary incontinence and their parents. The mobile application includes the training on urinary incontinence and urotherapy in children as well as all the test results of the child and ensures the follow-up of the children's compliance with the treatment. The developed mobile application is operatable on smartphones and tablets with Android and IOS operating systems.

This was followed by the second phase, during which the mobile application developed was pilot tested with 10 children. Based on the feedback received from the users, the mobile application was finalized.

Mobile application development process

  1. Content Creation For Goals
  2. Interface design development on MS Word and Photoshop
  3. Evaluation by specialists for content and design
  4. Converting to mobile application on Android and IOS platforms
  5. A pilot study with 10 children to evaluate the usability and suitability of the application
  6. Get feedback on the mobile app
  7. Based on this feedback, the mobile application was revised.
  8. Its final version was created

Study Type

Interventional

Enrollment (Actual)

10

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

      • Eskisehir, Turkey
        • Eskisehir Osmangazi University

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • The child has day and/or night urinary incontinence,
  • The child is between 7-12 years of age,
  • Family members and children can use mobile applications,
  • Family members have a smartphone,
  • The child and family members volunteers to participate in the study.

Exclusion Criteria:

  • The child has a mental or neurological disability,
  • The child has a developmental delay,
  • The child has previously received treatment for urinary incontinence,
  • The child has a communication problem,
  • The child has a history of surgery related to the urinary tract,
  • The child has a psychiatric diagnosis,
  • The child has a urinary tract infection,
  • The child has a radiological pathology on ultrasound,
  • The child has a diagnosis of neurogenic bladder.

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: pilot study
This was followed by the second phase, during which the mobile application developed was pilot tested with 10 children. Based on the feedback received from the users, the mobile application was finalized.
a mobile application was developed that can be used by children with urinary incontinence and their parents.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
mobile application development
Time Frame: six months
a mobile application was developed that can be used by children with urinary incontinence and their parents. The mobile application includes the training on urinary incontinence and urotherapy in children as well as all the test results of the child and ensures the follow-up of the children's compliance with the treatment. The developed mobile application is operatable on smartphones and tablets with Android and IOS operating systems.
six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
pilot tested
Time Frame: one month
This was followed by the second phase, during which the mobile application developed was pilot tested with 10 children. Based on the feedback received from the users, the mobile application was finalized.
one month

Collaborators and Investigators

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

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 15, 2020

Primary Completion (Actual)

February 15, 2021

Study Completion (Actual)

August 15, 2021

Study Registration Dates

First Submitted

April 3, 2023

First Submitted That Met QC Criteria

April 14, 2023

First Posted (Actual)

April 18, 2023

Study Record Updates

Last Update Posted (Actual)

April 18, 2023

Last Update Submitted That Met QC Criteria

April 14, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

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

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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