Stress urinary inconvenience. Stress incontinence (female) (male)
Conditions
Interventions
Intervention 1: Intervention group: They will receive 12 sessions of interferential currents 4 weeks, 3 times per week. The intensity of the interferential currents causes the torelated contractions.
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
No minimum to 65 Years
Inclusion criteria
Inclusion criteria: Have experienced stress urinary incontinence at least twice a week for two weeks. Stress urinary incontinence was confirmed by urodynamic tests and clinical examination. Mild and moderate stress urinary incontinence No history of taking anticholinergic drugs and other drugs during physiotherapy period.
Exclusion criteria
Exclusion criteria: smoking Known types of neuropathy Virginity Pregnancy and lactation History of pelvic surgery in the past year History of reconstructive surgery in the genitourinary system Having a urinary tract infection Chronic asthma and cough (more than three months) Having perceptual problems and mental illness based on a doctor's examination History of genitourinary neoplasia History of abnormalities in the genitourinary system Having any type of urinary incontinence other than pure stress urinary incontinence Severe stress urinary incontinence Severe prolapse Urethral hyper mobility Intrinsic sphincter dysfunction Severe neuromuscular disorders that compromise exercise performance
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean maximum intravaginal pressure. Timepoint: Immediately after allocation into , 4 and 8 weeks after starting treatment. Method of measurement: Pressure biofeedback.;Quality of life. Timepoint: Immediately after allocation into , 4 and 8 weeks after starting treatment. Method of measurement: ???? ???????? I_QOL.;ICIQ_UI SF questionnaire score. Timepoint: Immediately after allocation into , 4 and 8 weeks after starting treatment. Method of measurement: ICIQ_UI SF questionnaire.;Duration of maintenance of maximum intravaginal pressure. Timepoint: Immediately after allocation into , 4 and 8 weeks after starting treatment. Method of measurement: Pressure biofeedback.;Frequent urinary incontinence for a week. Timepoint: Immediately after allocation into , 4 and 8 weeks after starting treatment. Method of measurement: With bladder diary. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactReyhane Sekandari
Mashhad University of Medical Sciences
Outcome results
None listed