- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05721807
Physiotherapy in Stress Urinary Incontinence
Effectiveness of Functional Magnetic Stimulation and Pelvic Floor Muscle Training on Pelvic Floor Muscle Function, Urinary Incontinence Symptoms and Quality of Life in Women With Stress Urinary Incontinence
The goal of this randomized controlled trial is to evaluate and compare the effects of functional magnetic stimulation and pelvic floor muscle training on pelvic floor muscle function, urinary incontinence symptoms and quality of life in women with stress urinary incontinence. The main questions it aims to answer are:
- What is the effect of functional magnetic stimulation on pelvic floor muscle function, symptoms of urinary incontinence and quality of life in women with stress urinary incontinence?
- What is the effect of pelvic floor muscle training program on pelvic floor muscle function, symptoms of urinary incontinence and quality of life in women with stress urinary incontinence?
- Which intervention is more effective - functional magnetic stimulation or pelvic floor muscle training program?
Participants will be evaluated before and after the intervention with the following methods:
- International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF);
- Incontinence Impact Questionnaire-Short Form (IIQ-7);
- Pelvic floor muscle strength and endurance will be assessed with a "Pelvexiser" perineometer.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Kaunas, Lithuania
- Lithuanian Sports University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- complains of stress incontinence for at least 4 weeks;
- women who have given birth.
Exclusion Criteria:
- pregnancy;
- vaginism;
- urinal infection;
- oncological disorders;
- epilepsy;
- skin problems;
- if they had an implanted heart pacemaker, metal implants.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: functional magnetic stimulation
functional magnetic stimulation for stress urinary incontinence
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When applying functional magnetic stimulation, the stress urinary incontinence program "P2 stress" was chosen.
The first 20 min.
current frequency was 35 Hz, modulation - rising amplitude (from 0 to maximum per second), total wave duration 12 s.
active time 6 s., pause time 6 s.
After 20 min.
current frequency changed to 5 Hz, modulation and wave remained the same.
After 2 min.
current frequency changed to 35 Hz, modulation - amplitude, one-sided sinusoidal, wave remained the same.
The total duration of the procedure was 30 min.
A magnetic spring is installed at the bottom of the chair.
During the treatment, each subject was instructed to sit on a chair so that the perineum was centered on the spring and that the subjects felt the contraction of the muscles.
The intensity of the magnetic field was adjusted so as to feel comfortable during the study procedure (Vadalà et al., 2017).
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Experimental: pelvic floor muscle training program
exercise program for pelvic floor muscle
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The program consisted of two parts.
From procedures 1 to 6, 6 exercises were performed, after 6 times the exercises were adjusted, and from procedures 7 to 12, another 5 exercises were performed.
The program consists of breathing, pelvic floor muscle strength, endurance, speed training exercises and exercises to strengthen the thighs, buttocks, deep back and deep abdominal muscles.
Exercises were performed in 2 sets of 10 repetitions at an intensity from various positions: lying on the back, side, sitting, quadruped (Oliveira et al., 2017; Walton et al., 2019).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Urinary incontinence symptoms and quality of life (International Consultation on Incontinence Questionnaire)
Time Frame: Change from Baseline Urinary Incontinence symptoms at 6 weeks
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ICIQ - SF - International Consultation on Incontinence Questionnaire - Short Form is intended to subjectively evaluate the symptoms of urinary incontinence in a woman or man and the impact of those symptoms on the quality of life.
The questionnaire consists of four questions.
The first two questions assess the symptoms of urinary incontinence experienced, the third question describes quality of life and the fourth question determines which type of incontinence the person has.
The scores of the first three questions are summed up, the maximum number of points collected is 21, the minimum is 0. Depending on the number of points collected, the severity of urinary incontinence symptoms is assessed: no urinary incontinence symptoms (0 points), mild urinary incontinence symptoms (1 - 5 points), moderate incontinence symptoms (score 6-12), severe incontinence symptoms (score 13-18) and very severe incontinence symptoms (19-21).
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Change from Baseline Urinary Incontinence symptoms at 6 weeks
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IIQ-7 -Incontinence Impact Questionnaire
Time Frame: Change from Baseline Incontinence Impact Questionnaire scores at 6 weeks
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The IIQ-7 questionnaire is designed to assess the impact of urinary incontinence on quality of life.
The questionnaire consists of seven questions, which can be answered to find out the impact of urinary incontinence on all areas of life: physical activity, traveling, social activity, relationships, emotional state.
Each question is evaluated from 0 to 3 points.
The higher the score, the worse the quality of life.
The maximum number of collected points is 100, the minimum is 0. <50 points is considered a good quality of life, 50-70 points is an average quality of life, >70 points is a poor quality of life.
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Change from Baseline Incontinence Impact Questionnaire scores at 6 weeks
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Perineometry
Time Frame: Change from Baseline Perineometry at 6 weeks
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The strength and endurance of the subjects' pelvic floor muscles was assessed with a Pelvexiser perineometer (Wolfram Haboeck Co., Austria).
This apparatus has been scientifically proven as an objective method of assessing the function of the pelvic floor muscles and an effective exerciser for strengthening the pelvic floor muscles, which is why it is often used in the presence of for urinary incontinence problems.
The Pelvexiser can provide varying resistance to the pelvic floor muscles and provide real-time feedback on pelvic floor muscle contractions and changes (Chitra et al., 2010).
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Change from Baseline Perineometry at 6 weeks
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LithuanianSportsU-13
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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