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A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE

Primary Purpose

Urinary Incontinence

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Mobile Application
Sponsored by
Eskisehir Osmangazi University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Urinary Incontinence focused on measuring Mobile Application, Child, Quality of Life

Eligibility Criteria

7 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Eskisehir Osmangazi University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

pilot study

Arm Description

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.

Outcomes

Primary Outcome Measures

mobile application development
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.

Secondary Outcome Measures

pilot tested
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.

Full Information

First Posted
April 3, 2023
Last Updated
April 14, 2023
Sponsor
Eskisehir Osmangazi University
Collaborators
The Scientific and Technological Research Council of Turkey
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1. Study Identification

Unique Protocol Identification Number
NCT05815940
Brief Title
A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE
Official Title
A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE: PILOT STUDY
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
August 15, 2020 (Actual)
Primary Completion Date
February 15, 2021 (Actual)
Study Completion Date
August 15, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Eskisehir Osmangazi University
Collaborators
The Scientific and Technological Research Council of Turkey

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence
Keywords
Mobile Application, Child, Quality of Life

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
pilot study
Arm Type
Experimental
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Mobile Application
Intervention Description
a mobile application was developed that can be used by children with urinary incontinence and their parents.
Primary Outcome Measure Information:
Title
mobile application development
Description
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.
Time Frame
six months
Secondary Outcome Measure Information:
Title
pilot tested
Description
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.
Time Frame
one month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Facility Information:
Facility Name
Eskisehir Osmangazi University
City
Eskisehir
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE

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