About this trial
The study aimed to explore the link between urinary incontinence (UI) severity in patients with multiple sclerosis (PwMS), electromyography (EMG) findings, and other relevant factors.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
having an MS diagnosis according to the 2017 revised McDonald criteria,
experiencing symptoms of UI as defined by the International Continence Society (ICS),
having an EDSS score below 6.5,
PwMS with no communication issues.
Disqualifiers
PwMS who did not give consent to participate,
those with medication changes in the past 6 months,
pregnant PwMS,
recent vaginal or caesarean deliveries within 6 months,
Trial population
Women diagnosed with MS will be included in the study.
Trial design
Other
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Expanded disability status scale (EDSS)
The Expanded disability status scale (EDSS) will be assessed disability and progression in PwMS, with scores from 0 (normal neurological exam) to 10 (death from MS). Higher scores indicate greater disability.
Neurogenic Bladder Symptom Score (NBSS)
Storage, voiding, and complication symptoms of neurogenic bladder will be assessed with the Neurogenic Bladder Symptom Score (NBSS), a 24-item questionnaire covering incontinence, storage and voiding, and outcomes.
International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF)
The frequency and amount of leakage will be assessed using a six-item scale, and urinary incontinence will be categorised into four groups: mild (1-5), moderate (6-12), severe (13-18) and very severe.
Incontinence Impact Questionnaire (IIQ-7)
Urinary symptoms' impact on daily activities was assessed with the Incontinence Impact Questionnaire (IIQ-7). The 7-item Likert scale has a score range of 0-21, with higher scores reflecting an increased negative impact of incontinence on social functioning, quality of life, and physical activity.
Sponsors and contacts
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