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Early Detection of OAB and Elimination of Negative Impact on Quality of Life

Early Detection of Overactive Bladder and Elimination of Negative Impact on Quality of Life

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07371000
Enrollment
1000
Registered
2026-01-27
Start date
2025-09-01
Completion date
2026-08-31
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overactive Bladder (OAB)

Keywords

Overactive bladder, Screening, Telemedicine, Online screening tool

Brief summary

Overactive bladder (OAB) is one of the most common health problems in the adult population. The goal of this project is to improve the awareness of the problem and to correctly refer the targeted persons to a specialist or a doctor. This will be provided by an online screening tool, designed as web platform and mobile application, where the data will be stored in respect to GDPR. People with a positive result from the online screening tool will be offered an examination by a specialist (gynaecologist, urogynaecologist, urologist) involved in the project. The specialist will have access to the results from the online screening tool - he/she will log into the web platform with a view of the participants profile. He/she will perform the diagnosis, confirm or refute the diagnosis and complement it with any further diagnostic tests and set the standard treatment.

Detailed description

Overactive bladder (OAB) is one of the most common health problems in the adult population (15-20% prevalence), with just under half of those affected seeking professional medical help. The goal of this project is to improve the awareness of the problem and to correctly refer the targeted participants to a specialist or a doctor who is knowledgeable about the problem and who will set up an adequate therapy. A targeted PR campaign will direct those interested in joining the pilot screening project to a website with information about OAB and information about the pilot screening process. The web platform will also guide the user to create a secure user profile to participate in the project, where they will complete validated questionnaires related to OAB, necessary personal and family history data to optimize follow-up diagnosis during the in-person examination with a specialist, and a validated questionnaire measuring quality of life. After completing the online screening tool, the user will be offered a referral to a specialist in the vicinity. Participation in the online screening tool will be conditional on checking the online Consent to Participate box and Consent to Disclose Personal Data in accordance with GDPR. People with a positive result from the online screening tool will be offered an examination by a specialist (gynaecologist, urogynaecologist, urologist) involved in the project. The specialist will have access to the results from the online screening tool - he/she will log into the web platform with a view of the participant's profile. He/she will perform the diagnosis, confirm or refute the diagnosis and complement it with any further diagnostic tests and set the standard treatment. The data collected will be used to properly evaluate the pilot project in line with its objectives. An analysis of the problems and risks of the project with regard to the whole pilot screening process and a simplified cost evaluation will also be carried out.

Interventions

OTHERStandardized Screening Protocol

After completing the online screening tool (including validated questionnaires), selected participants are offered an appointment with a specialist who will perform a diagnosis, confirm or rule out OAB and set up adequate therapy according to recommended procedures.

Sponsors

Institute of Health Information and Statistics of the Czech Republic
Lead SponsorOTHER_GOV
General University Hospital, Prague
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Signed Consent to Participate in the Project and Consent to the Processing of Personal Data (online and paper format) * Men and women over 18 years of age with increased urinary frequency (more than 7 times in 24 hours) Optional inclusion criteria: \- Nycturia and/or urge incontinence.

Exclusion criteria

* Unsigned Consent to Participate in the Project and Consent to the Processing of Personal Data. * Current treatment of OAB, acute problems, suspicion of another disease causing OAB symptoms (haematuria, suspected bladder cancer, etc.) * Inflammation of the lower urinary tract.

Design outcomes

Primary

MeasureTime frameDescription
Pilot testing with 1,000 participantsFrom enrollment to the end of examination in 3 monthsPilot testing of the procedure on a sample of 1,000 people who will undergo an online self-diagnostic screening tool and be examined by a urogynecologist/urologist.
Number of participants (completion of anonymous screening test)from enrollment up to 1 weekNumber of participants who complete anonymous screening test based on three questions reffering to urology health
Percentage of people with suspected OAB who agreed to participate in a follow-up examination with specialistFrom enrollment up to 3 months
Percentage of people with a specialist confirmed diagnosis of OAB at the face-to-face visitThrough study completion, an average of 6 months
Percentage of people who attended follow-up examination after 3 monthsThrough study completion, an average of 9 months

Countries

Czechia

Contacts

CONTACTKateřina Ondrášková, Msc
katerina.ondraskova@uzis.cz604603143
CONTACTLucie Mandelová, PhD
lucie.mandelova@uzis.cz
STUDY_DIRECTORJaromír Mašata, Professor

General University Hospital of Prague

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026