Actively Recruiting
Use of Virtual Reality in the Treatment of Various Types of Urinary Incontinence in Women
Led by Wroclaw University of Health and Sport Sciences · Updated on 2025-07-24
40
Participants Needed
1
Research Sites
89 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 research aims to evaluate the use of virtual reality (VR) to support pelvic floor muscle training in women with urinary incontinence (UI). It focuses on improving motivation, awareness, and exercise accuracy through real-time muscle visualization and immersive interaction. The trial compares VR-assisted therapy to conventional approaches to determine if it improves clinical outcomes for women aged 50 to 80 years who have UI of mild to moderate severity. The study includes two groups: one receiving eight sessions of VR therapy over two weeks using a head-mounted display creating an immersive therapeutic garden environment, and the other receiving eight sessions of pelvic floor muscle electrostimulation with EMG biofeedback during the same period. Both interventions are delivered four times per week, with VR sessions lasting 20 minutes and electrostimulation sessions lasting 30 minutes. The VR system provides a multi-sensory experience designed to enhance engagement, while the biofeedback device offers real-time visual feedback to support correct muscle activation. Participants will undergo assessments before and after the two-week treatment to measure changes in quality of life, urinary incontinence severity, pelvic organ prolapse, bladder function, stress levels, and self-esteem. Various questionnaires and clinical evaluations will be used to track progress. The primary outcome is the change in the Incontinence Quality of Life Questionnaire score at two weeks. Safety and adherence will be monitored throughout, and the total participation time is approximately two weeks from enrollment to the end of treatment.
CONDITIONS
Brief Title
Virtual Reality for Urinary Incontinence in Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 50 to 80 years
- At least 12 months post-menopausal
- Diagnosed with urinary incontinence grade I or IIa according to ICS classification
- No contraindications such as acute urinary tract infections or severe neurological disorders
- Provided written informed consent to participate
You will not qualify if you...
- Urinary incontinence grade III or higher
- Significant neurological conditions affecting bladder control
- Participation in other therapeutic interventions that might affect 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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 weeks
Participants receive eight sessions of therapy over two weeks. Those in the experimental group undergo virtual reality-supported pelvic floor muscle training with immersive biofeedback. Participants in the control group receive conventional pelvic floor muscle training with electrostimulation and EMG biofeedback.
Eight sessions over two weeks (four sessions per week)
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
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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