Actively Recruiting
Virtual Reality for Urinary Incontinence in Women
Led by Wroclaw University of Health and Sport Sciences · Updated on 2025-07-24
40
Participants Needed
1
Research Sites
100 weeks
Total Duration
On this page
Sponsors
W
Wroclaw University of Health and Sport Sciences
Lead Sponsor
I
Independent Public Health Care Center of the Ministry of the Interior and Administration in Wrocław
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study evaluates the effectiveness of using virtual reality to support pelvic floor muscle training in women with urinary incontinence. The intervention aims to enhance patients' motivation, awareness, and exercise accuracy through real-time muscle visualization and immersive interaction. The project seeks to determine whether virtual reality-assisted therapy improves clinical outcomes compared to conventional approaches.
CONDITIONS
Official Title
Virtual Reality for Urinary Incontinence in Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 50 to 80 years who are at least 12 months post-menopausal
- Diagnosed with urinary incontinence of grade I or IIa according to the ICS classification
- No contraindications to participation such as acute urinary tract infections or severe neurological disorders
- Provided written informed consent to participate in the research experiment
You will not qualify if you...
- Urinary incontinence of grade III or higher
- Presence of significant neurological conditions affecting bladder control
- Participation in other therapeutic interventions that could interfere with study outcomes
- Pregnancy
- Refusal or inability to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Independent Public Health Care Center of the Ministry of the Interior and Administration in Wrocław
Wroclaw, Lower Silesian Voivodeship, Poland, 50-233
Actively Recruiting
Research Team
G
Gabriela Kołodyńska, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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