Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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
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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