Effects of Electrical Stimulation on Overactive Bladder in Women
Investigation of Effects of External Electrical Stimulation in Women With Vaginal Laxity
This study is testing if different types of electrical stimulation can help women with overactive bladder feel better and improve their quality of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Selcuk University Academic / other |
| Locations | 1 site (Konya) |
| Trial ID | NCT06935240 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of various externally applied electrical stimulation methods on symptoms of overactive bladder (OAB) in women. It compares the effectiveness of transcutaneous electrical nerve stimulation (TENS) and neuromuscular electrical stimulation (Innovo) in improving quality of life and patient-reported outcomes. Participants will use a portable TENS device designed to modulate neural pathways affecting bladder control. The study aims to provide insights into non-invasive treatment options for OAB.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18-65 diagnosed with overactive bladder.
Not a fit: Patients with sensory loss, infections, or serious cardiovascular problems may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could offer women with overactive bladder a non-invasive treatment option that improves their symptoms and quality of life.
How similar studies have performed: Previous studies have shown promise with electrical stimulation techniques for bladder control, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: To be between the ages of 18-65 Being diagnosed with AAM Volunteer Becoming literate Exclusion Criteria: Sensory loss Presence of infection Having a pacemaker Metal implant presence Malignancy story Having serious cardiovascular problems Presence of severe pelvic organ prolapse (above stage 2) Pregnancy presence Lumbosacral peripheral nerve lesion
Where this trial is running
Konya
- Selcuk University — Konya, Turkey (Türkiye) (Recruiting)
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.