Effects of bladder training and pelvic floor exercises with Botox on urinary symptoms
Official title: Effect of Bladder Training and Pelvic Floor Exercise Training on Urinary Symptoms and Quality of Life in Patients With Overactive Bladder Syndrome
Run by Hacettepe University · NCT06209333 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing if adding bladder training and pelvic floor exercises to Botox treatment can help people with Overactive Bladder Syndrome feel better compared to just getting Botox alone.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Hacettepe University Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06209333 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults over 18 with non-neurogenic Overactive Bladder Syndrome who have not responded to conservative treatments.
✕Probably not a fit
Patients with neurogenic bladder issues, pregnant women, or those with certain anatomical abnormalities will 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 examines the impact of combining bladder training and pelvic floor exercise with Botulinum Toxin-A (BTx-A) treatment in patients suffering from Overactive Bladder Syndrome (OABS) who have not responded to conservative therapies. Participants will be divided into two groups: one receiving BTx-A along with the additional training and the other receiving only BTx-A with standard education. The study aims to evaluate urinary symptoms and quality of life before and after treatment at specified intervals. The goal is to determine if the combined approach leads to better outcomes than BTx-A alone.
Why it matters
Potential benefit: If successful, this approach could significantly improve urinary symptoms and quality of life for patients with OABS.
How similar studies have gone: While similar approaches have been explored, this specific combination of interventions is relatively novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * over the age of 18 (those with a Mini Mental Test score of 24 and above for individuals over the age of 65), * Who has Non-Neurogenic Overactive Bladder Syndrome, * Patients who received Routine Botulinum Toxin-A administration because they did not respond to conservative treatment, * Patients who volunteer to participate in the study will be included. Exclusion Criteria: * Patients with Neurogenic Overactive Bladder Syndrome, * Pregnant Women, * Lack of cooperation in evaluation and/or treatment and lack of literacy status, * Patients with urogynocological/anatomical abnormalities, * Patients receiving pelvic radiation therapy, * Patients with psychiatric or neurogenic disorders and * Patients who have not given consent to the study and do not have an informed consent form (BGOF).
Where it's running
-
Aslı Aslan
Ankara, Turkey Recruiting
Study contacts
- Study coordinator: Ceren Gursen, associate professor
- Email: cerengursen@yahoo.com
- Phone: +905380644120
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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.