Turkish Version of the Neurogenic Bladder Symptom Score Short Form

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGaziantep Islam Science and Technology University

About this trial

This observational study aims to evaluate the cross-cultural adaptation and psychometric properties of the Turkish version of the Neurogenic Bladder Symptom Score Short Form (NBSS-SF) in adults with spinal cord injury or multiple sclerosis who have neurogenic lower urinary tract dysfunction. Neurogenic bladder symptoms, such as urinary incontinence, urgency, and difficulties with urine storage or emptying, may negatively affect daily functioning and quality of life. In this study, the validity and reliability of the Turkish NBSS-SF will be examined, and convergent validity will be assessed through its relationship with the King's Health Questionnaire (KHQ) and the Short Form-12 (SF-12). In eligible participants, the scale will be administered again after 7 to 14 days. The aim of the study is to provide a valid and reliable Turkish patient-reported outcome measure for use in clinical practice and research.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.)

Disqualifiers

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

Trial population

The study will be conducted on patients aged ≥18 years with neurogenic LUTS diagnosed with MS or SCI.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 1 trial group
Group A: Patients diagnosed with Spinal Cord Injury (SCI) or Multiple Sclerosis (MS) and neurogenic lower uri

Trial outcomes

Primary outcomes

1

Neurogenic Bladder Symptom Score Short Form (NBSS-SF) total score

The Neurogenic Bladder Symptom Score Short Form (NBSS-SF) is a 10-item patient-reported outcome measure. It will be evaluated in adults with spinal cord injury or multiple sclerosis who have neurogenic lower urinary tract dysfunction. The NBSS-SF total symptom score ranges from 0 to 28, with lower scores indicating better symptom status and higher scores indicating worse symptom burden. Domain scores for incontinence, storage and voiding, and consequences will also be assessed. Psychometric evaluation will include internal consistency, test-retest reliability, and convergent validity.

Time frame
3 months

Secondary outcomes

Other outcomes

1

King's Health Questionnaire (KHQ) domain scores

The King's Health Questionnaire (KHQ) will be used to assess convergent validity of the Turkish version of the Neurogenic Bladder Symptom Score Short Form (NBSS-SF). KHQ domain scores will be analyzed, with higher scores indicating worse health-related quality of life and greater symptom impact.

Time frame
3 months
2

12-Item Short Form Health Survey (SF-12) mental and physical health subscale scores

The 12-Item Short Form Health Survey (SF-12) will be used to assess convergent validity of the Turkish version of the Neurogenic Bladder Symptom Score Short Form (NBSS-SF). Mental and physical health subscale scores will be analyzed separately, with higher scores indicating better health-related quality of life.

Time frame
3 months

Locations

This trial has no locations.

Sponsors and contacts

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