Stress Urinary Incontinence
Conditions
Interventions
Group A: 15 women with post-menopausal stress urinary incontinence will be treated with vaginal pressure biofeedback. The patients will perform 3 series of 10 isometric contractions of 2, 4 or 8 secon
Other
E02.779
Sponsors
SOBEU - Associação Barramansense de Ensino
Centro Universitário de Barra Mansa
Eligibility
Sex/Gender
Female
Age
40 Years to 90 Years
Inclusion criteria
Inclusion criteria: Age range between 40 and 90 years; minimum period of one year of amenorrhea before the evaluation; without cognitive and or communication problem; who agree to participate in the study according to the informed consent.
Exclusion criteria
Exclusion criteria: Patients less than 40 years and older than 90 years; continents; who have urinary incontinence other than effort; have neurological; visual; auditory; cognitive; oncological; prolapse; intact hymen; vaginal narrowing; vaginal or urinary infection; gynecological uterus; recent gynecological surgery; skin lesions or diseases; allergic processes to the functional elastic bandage or the condom used; musculoskeletal conditions that prevent the performance of the tests and or treatment; being in another physiotherapeutic treatment for the pelvic floor musculature and who refuse to sign the free and informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increase muscle strength of the pelvic floor observed through the Ortiz scale and pressure perineometer and improvement in quality of life verified through the International Consultation on Incontinence Questionnaire Short Form or ICIQ SF and Incontinence Quality of life Questionnaire or I-QoL questionnaire. from the observation d a variation of at least 5% in the pre and post intervention measurements. Data collected before and after the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Increase muscle strength of the pelvic floor observed through the Ortiz scale and pressure perineometer and improvement in quality of life verified through the International Consultation on Incontinence Questionnaire Short Form or ICIQ SF and Incontinence Quality of life Questionnaire or I-QoL questionnaire. from the observation d a variation of at least 5% in the pre and post intervention measurements. Data collected before the intervention and one month after the intervention. | — |
Countries
Brazil
Contacts
Public ContactAriela Torres Cruz
Centro Universitário de Barra Mansa
Outcome results
None listed