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Effects of Digital Pelvic Floor Muscle Training in Patients With Multiple Sclerosis Having Lower Urinary Tract Symptoms

Effects of Digital Pelvic Floor Muscle Training and Lifestyle Recommendations in Patients With Multiple Sclerosis Having Lower Urinary Tract Symptoms

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04759391
Enrollment
30
Registered
2021-02-18
Start date
2021-02-28
Completion date
2021-07-31
Last updated
2021-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower Urinary Tract Symptoms

Keywords

Lower Urinary Tract Symptoms, Multiple Sclerosis, Pelvic Floor Muscle Training

Brief summary

The aim of this study was to investigate the effects of digital pelvic floor muscle training and lifestyle recommendations in patients with Multiple Sclerosis having lower urinary tract symptoms.

Detailed description

Multiple sclerosis (MS) is an autoimmune, neurodegenerative disease of the central nervous system. Lower urinary tract symptoms (LUTS) are very common in MS. Pelvic floor muscle training (PFMT) is one of the first-line choices for the conservative treatment of LUTS. According to our knowledge, no study has investigated the effects of digital pelvic floor muscle training and lifestyle recommendations in MS having LUTS, yet.

Interventions

OTHERExercise

Pelvic floor muscle training program planned under the supervision of a physiotherapist was applied and followed to the exercise group, using the digital application.

Information was given within the scope of lifestyle recommendations (fluid intake, diet, constipation, weight control, smoking related to lower urinary system symptoms

Sponsors

Ataturk Training and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will be randomly divided into two groups (control and exercise) for treatment.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Having a diagnosis of MS and having at least two of the lower urinary symptoms * Not having an attack in the last 1 month, * No change in medical treatment in the last 3 months * Expanded disability status scale-EDSS score is less than 6.5 * Not having any cognitive problems that would hinder cooperation and understanding * Those who use digital devices such as computers, laptops, smartphones and tablets * Volunteering to participate in the study

Exclusion criteria

* Pregnancy status * Active urinary tract infection * Another neurological disease that can cause incontinence * A history of malignancy * Prostate surgery * Those with missing evaluation parameters * Those who do not regularly participate in treatment programs

Design outcomes

Primary

MeasureTime frameDescription
Incontinence symtomschange from baseline at 8 weeksUrinary incontinence symptoms will be evaluated with The International Consultation of Incontinence Questionnaire - Short Form
Overactive bladder symptomschange from baseline at 8 weeksOveractive bladder symptoms will be evaluated with Overactive Bladder Questionnaire-Version8

Secondary

MeasureTime frameDescription
bladder functionschange from baseline at 8 weeksbladder functions will be evaluated with voiding diary
Quality of life levelchange from baseline at 8 weeksQuality of life will be evaluated with King's Health Questionnaire
subjective perception of improvementafter treatment (8th week)subjective perception of improvement will be evaluated with a 4-item Likert-type scale
patient satisfactionafter treatment (8th week)patient satisfaction will be evaluated with a 5-item Likert-type scale

Countries

Turkey (Türkiye)

Contacts

Primary ContactSeyda Toprak Celenay
sydtoprak@hotmail.com+90312 906 1000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026