Identification of Factors Related to UI in Patients With MS and EMG Assessment of PFM Activity

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age30-50
SponsorArtvin Coruh University

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 volunteers

Qualifiers

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

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

47 Participants
are grouped into 1 trial group
Group A: Patients with Multiple Sclerosis (PwMS)

Trial outcomes

Primary outcomes

1

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.

Time frame
Single assessment at enrollment
2

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.

Time frame
Single assessment at enrollment
3

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.

Time frame
Single assessment at enrollment
4

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.

Time frame
Single assessment at enrollment

Secondary outcomes

Other outcomes

Sponsors and contacts

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