Telerehabilitation for Women with Urinary Incontinence
The Effectiveness of a Blended Synchronous and Asynchronous Telerehabilitation Program for Greek Adult Women With Urinary Incontinence. A Randomized Controlled Trial
NA · University of Patras · NCT06848517
This study is testing if online rehabilitation programs can help women in Greece with urinary incontinence feel better compared to traditional therapy and no support at all.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | Female |
| Sponsor | University of Patras (other) |
| Locations | 1 site (Pátrai, Rion, Achaia) |
| Trial ID | NCT06848517 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of synchronous and asynchronous telerehabilitation programs for women suffering from urinary incontinence in Greece. Participants will be divided into three groups: one receiving blended telerehabilitation, another undergoing face-to-face sessions with a therapist, and a control group with no supervision. The study aims to improve adherence to pelvic floor muscle training through interactive online platforms. Assessments will occur at baseline, 6 weeks, and 12 weeks, with follow-ups at 6 and 9 months.
Who should consider this trial
Good fit: Ideal candidates are Greek women aged 18-75 diagnosed with stress urinary incontinence or mixed urinary incontinence.
Not a fit: Patients who have had major gynecological surgery in the last 10 years or have systemic diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance treatment adherence and outcomes for women with urinary incontinence.
How similar studies have performed: Other studies have shown promise in using telerehabilitation for various conditions, suggesting potential success for this approach in urinary incontinence treatment.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Greek women, * 18-75 years old, * Diagnosis of Stress Urinary Incontinence (SUI) or Mixed UI (via Urodynamic examination). * Writing and reading of the Greek language * Having ease in using synchronous communication platforms (e.g., Zoom) and asynchronous educational videos via smart phones, tablets, computers etc * Able to voluntarily contract the PFM, during the initial clinical examination. Exclusion Criteria: * 6 months after postpartum, * Systemic diseases * Malignancy, * Major gynecological surgery (i.e. total hysterectomy) over the last 10 years, * Neurological dysfunction, * Mental impairment
Where this trial is running
Pátrai, Rion, Achaia
- University of Patras, School of Health Rehabilitation Science, Department of Physiotherapy — Pátrai, Rion, Achaia, Greece (RECRUITING)
Study contacts
- Principal investigator: Dimitra-Tania Papanikolaou — University of Patras
- Study coordinator: Evdokia Billis, Professor
- Email: billis@upatras.gr
- Phone: 6973047170
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Urinary Incontinence,Stress