Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07371000

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

Led by Institute of Health Information and Statistics of the Czech Republic · Updated on 2026-01-27

1000

Participants Needed

20

Research Sites

8 weeks

Total Duration

On this page

Sponsors

I

Institute of Health Information and Statistics of the Czech Republic

Lead Sponsor

G

General University Hospital, Prague

Collaborating Sponsor

AI-Summary

What this Trial Is About

Overactive bladder (OAB) is a common health issue affecting 15-20% of adults, but less than half seek medical help. This research aims to raise awareness of OAB and improve referrals to specialists who can provide appropriate diagnosis and treatment. The project is led by the Institute of Health Information and Statistics of the Czech Republic and focuses on early detection and reducing the negative impact of OAB on quality of life. The study uses an online screening tool available via a web platform and mobile app, where participants complete validated questionnaires related to OAB symptoms, personal and family history, and quality of life. Those with positive screening results are offered an examination by specialists such as gynecologists, urogynaecologists, or urologists. Specialists access participant profiles through the platform, confirm or rule out OAB, perform additional diagnostic tests if needed, and set up standard treatments. Participation requires consent to data processing under GDPR. Participants will provide data through the online tool and may attend follow-up examinations with specialists. The study tracks outcomes including the number of participants completing the screening, those agreeing to specialist visits, confirmed diagnoses, and follow-up attendance over an average period of six to nine months. Data collected will evaluate the pilot project’s effectiveness and cost, with all information stored securely respecting privacy regulations.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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: presence of nycturia and/or urge incontinence
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to 3 months

Participants who screen positive online are offered an in-person examination by a specialist to confirm or rule out overactive bladder and to set up adequate therapy.

1 in-person visit with a specialist

Long-term Monitoring

Duration - Up to 9 months

Participants diagnosed with overactive bladder may be monitored for follow-up evaluation and assessment of treatment impact.

Follow-up visits may occur depending on treatment and specialist recommendation

Trial Site Locations

Total: 20 locations

1

Brno University Hospital

Brno, Czechia

Not Yet Recruiting

2

GYN-LINE, s.r.o.

Brno, Czechia

Not Yet Recruiting

3

České Budějovice Hospital

České Budějovice, Czechia

Not Yet Recruiting

4

Hospital Hořovice

Hořovice, Czechia

Not Yet Recruiting

5

University Hospital Hradec Králové

Hradec Králové, Czechia

Not Yet Recruiting

6

Hospital Jablonec nad Nisou

Jablonec nad Nisou, Czechia

Not Yet Recruiting

7

AGYNO s.r.o.

Karlovy Vary, Czechia

Not Yet Recruiting

8

Oblastní nemocnice Kolín a.s.

Kolín, Czechia

Not Yet Recruiting

9

Olomouc University Hospital

Olomouc, Czechia

Not Yet Recruiting

10

GYNOVA s.r.o.

Ostrava, Czechia

Not Yet Recruiting

11

Hospital AGEL Ostrava - Vítkovice a.s.

Ostrava, Czechia

Not Yet Recruiting

12

University Hospital Ostrava

Ostrava, Czechia

Not Yet Recruiting

13

Gyncare Michael Švec s.r.o.

Pilsen, Czechia

Not Yet Recruiting

14

Mulačova nemocnice

Pilsen, Czechia

Not Yet Recruiting

15

General University Hospital

Prague, Czechia

Actively Recruiting

16

GynUp! s.r.o.

Prague, Czechia

Not Yet Recruiting

17

University Hospital Bulovka

Prague, Czechia

Not Yet Recruiting

18

University Thomayer Hospital

Prague, Czechia

Not Yet Recruiting

19

Uroklinikum s.r.o.

Prague, Czechia

Not Yet Recruiting

20

Sokolov Hospital

Sokolov, Czechia

Not Yet Recruiting

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Research Team

K

Kateřina Ondrášková, Msc

L

Lucie Mandelová, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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