- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05815940
A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE
A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE: PILOT STUDY
Study Overview
Status
Conditions
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
- 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
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Eskisehir, Turkey
- Eskisehir Osmangazi University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- EskisehirOU-cakirli-2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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