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Pilates Training and Low Intensity Shock Wave Therapy for Post-prostatectomy Stress Incontinence

Not Applicable
Conditions
Stress Incontinence, Male
Registration Number
NCT06322082
Lead Sponsor
Khadra Mohamed Ali
Brief Summary

120 Patients with urinary incontinence following radical prostatectomy would be randomly assigned to either 4 groups all receive conventional pelvic floor muscle exercises plus group A receive Pilates exercises and Low Intensity Extracorporeal Shock Wave Therapy, group B receive Low Intensity Extracorporeal Shock Wave Therapy, group C receive Pilates exercises and group D receive conventional pelvic floor muscle exercises. Assessment at baseline, immediately after the intervention, to evaluate the degree of urinary incontinence and quality of life after three months from treatment.

Detailed Description

120 Patients with urinary incontinence following radical prostatectomy would be randomly assigned to either 4 groups all receive conventional pelvic floor muscle exercises plus group A receive Pilates exercises and Low Intensity Extracorporeal Shock Wave Therapy, group B receive Low Intensity Extracorporeal Shock Wave Therapy, group C receive Pilates exercises and group D receive conventional pelvic floor muscle exercises. Assessment at baseline, immediately after the intervention, to evaluate the degree of urinary incontinence by Urodynamic investigation system, Severity index scale and Cytometry and quality of life by The quality of life questionnaire IQOL after three months from treatment.

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
Male
Target Recruitment
120
Inclusion Criteria
  • All patients diagnosed as urinary incontinence.
  • Age between 40 -75 male patients or older.
  • All patients received the same medical treatment
Exclusion Criteria
  • adjuvant or neoadjuvant chemo-radiation therapy.
  • severe postoperative complications.
  • history of pelvic surgery, and diseases that could affect voiding function and limitations for the exercise program such as for patients with serious cardiovascular events or spinal or articular disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Cystometrybefore treatment and after 3 months

Ithe dynamic measurement of detrusor pressure during the continuous filling of the bladder.

Severity index scalebefore treatment and after 3 months

measure frequency and amount of urine loss ,calculated by this equation: Severity index of incontinence = (Points for frequency of urine loss) × (Points for amount of urine loss) calculated by this equation: Severity index of incontinence = (Points for frequency of urine loss) × (Points for amount of urine loss) measure frequency and amount of urine loss to calculate severity of incontinence, o Frequency of urine loss grades: Never = 0 less than once a month= 1 once to several times a month = 2 once to several times a week = 3 Every day and/or night = 4

* o Amount of urine loss grades: No drop (completely dry) = 0 A few drops = 1 A little = 2 More = 3

Secondary Outcome Measures
NameTimeMethod
body mass indexbefore treatment and after 3 months

measure ( weight per height squares )of patients kg/m\^2

Trial Locations

Locations (1)

faculty of physical therapy , Cairo university

🇪🇬

Giza, Egypt

faculty of physical therapy , Cairo university
🇪🇬Giza, Egypt

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