Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
FEMALE
ID07070063

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

Age: 50Years - 80Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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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