New turkish questionnaire aims to better measure bladder symptoms in neurological patients
NCT ID NCT07507331
First seen Jun 27, 2026 · Last updated Jul 24, 2026 · Updated 2 times
Summary
This study is translating and testing a short questionnaire called the Neurogenic Bladder Symptom Score Short Form (NBSS-SF) into Turkish. It will involve 120 adults with spinal cord injury or multiple sclerosis who have bladder problems. The goal is to make sure the Turkish version is accurate and reliable for use in clinics and research.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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120 people
The number who actually took part.
- Started
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Mar 2026
- Finished
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Jul 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study will be conducted on patients aged ≥18 years with neurogenic LUTS diagnosed with MS or SCI.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Being ≥18 years old * Having a diagnosis of Spinal Cord Injury (SCI) or Multiple Sclerosis (MS) and neurogenic lower urinary tract dysfunction * Being able to read and understand Turkish and have the cognitive ability to independently complete questionnaires * Can be included with any bladder management method (spontaneous voiding, CIC, permanent catheter, condom catheter, reconstruction/diversion etc.) * Volunteering and signing informed consent Exclusion Criteria: * Having an active urinary tract infection (UTI) * Having undergone urological surgery in the last month * Reporting changes in bladder/urinary function between the first and second applications (surgery, UTI, change in bladder medication) * Having a significant recent change in general health status * Having a spinal cord injury (SCI) in the spinal shock phase * Having experienced a relapse of Multiple Sclerosis (MS) within the last 3 months.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hacettepe University Hospital, Neurology Outpatient Clinic and Viransehir State Hospital, Urology Outpatient Clinic
Ankara, Çankaya, 06100, Turkey (Türkiye)
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