A MOBILE APPLICATION DEVELOPED FOR CHILDREN WITH URINARY INCONTINENCE

NCT ID: NCT05815940

Last Updated: 2023-04-18

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

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-08-15

Study Completion Date

2021-08-15

Brief Summary

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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

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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

Conditions

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Urinary Incontinence

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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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.

Group Type EXPERIMENTAL

Mobile Application

Intervention Type BEHAVIORAL

a mobile application was developed that can be used by children with urinary incontinence and their parents.

Interventions

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Mobile Application

a mobile application was developed that can be used by children with urinary incontinence and their parents.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

7 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Scientific and Technological Research Council of Turkey

OTHER

Sponsor Role collaborator

Eskisehir Osmangazi University

OTHER

Sponsor Role lead

Responsible Party

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Merve Çakırlı

Research Assisstant

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Eskisehir Osmangazi University

Eskişehir, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Acikgoz A, Cakirli M, Tokar B, Celik O. SunCloud: A mobile application for children with urinary incontinence. J Eval Clin Pract. 2025 Feb;31(1):e14122. doi: 10.1111/jep.14122. Epub 2024 Aug 7.

Reference Type DERIVED
PMID: 39113266 (View on PubMed)

Other Identifiers

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EskisehirOU-cakirli-2

Identifier Type: -

Identifier Source: org_study_id

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