Telerehabilitation for Women with Urinary Incontinence
Official title: The Effectiveness of a Blended Synchronous and Asynchronous Telerehabilitation Program for Greek Adult Women With Urinary Incontinence. A Randomized Controlled Trial
Run by University of Patras · NCT06848517 · Data updated 2026-11-12
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
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | Women only |
| Enrollment | 60 (estimated) |
| Sponsor | University of Patras Academic / other |
| Locations | 1 site (Pátrai, Rion, Achaia) |
| Status | Recruiting |
| Started | February 15, 2025 |
| Main results expected | September 30, 2025 |
| Study ends | May 30, 2026 |
| Registry record updated | February 27, 2025 |
| Trial ID | NCT06848517 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are Greek women aged 18-75 diagnosed with stress urinary incontinence or mixed urinary incontinence.
✕Probably 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.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: Other studies have shown promise in using telerehabilitation for various conditions, suggesting potential success for this approach in urinary incontinence treatment.
Who can join: the full rules
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 it's running
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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
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Orforglipron for women with stress urinary incontinence who are overweight or have obesity
This trial will test whether orforglipron reduces urine leakage in adult women with stress urinary incontinence who are overweight or have obesity.
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Using TENS for pain relief during outpatient urethral bulking in women with stress urinary incontinence.
This study is testing if using a TENS machine can help reduce pain for women undergoing a specific procedure for stress urinary incontinence.
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Adjustable Continence Therapy for treating female stress urinary incontinence
This study is testing a new treatment called Adjustable Continence Therapy to see if it can help women with stress urinary incontinence who haven't had success with other treatments.
-
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This study tests whether increasing running cadence by about 10% for eight weeks can reduce stress urinary incontinence symptoms in parous women who run regularly and own a Garmin watch.
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Prophylactic antibiotics to reduce post-procedure UTIs after urethral bulking
We’re testing whether giving a preventive antibiotic at the time of urethral bulking can lower the chance of a urinary tract infection after the procedure for women with stress or mixed urinary incontinence.
-
Evaluating the impact of different mesh widths in surgery for urinary incontinence
This study is testing whether using a wider surgical mesh during surgery for urinary incontinence in women can lead to better results and fewer problems.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.