Urinary incontinence.
Conditions
Interventions
105 volunteers aged between 18 and 80 will participate in this study. They will be divided randomly into the following groups according to the type of electrical current: urogynecological TENS group (
Other
E02.331.800
Sponsors
Universidade Estadual Paulista, Instituto de Biociências
Universidade Estadual Paulista
Eligibility
Sex/Gender
Female
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: For the present study, all women who present complaints of Bladder Hyperactivity with increased urinary frequency, nocturia or urge-incontinence; negative diagnosis for low urinary tract infections; mixed urinary incontinence.
Exclusion criteria
Exclusion criteria: Criteria for non-inclusion will be cognitive deficit; psychiatric disorders; pregnancy; diagnosis of neurogenic bladder; prolapse of pelvic organs above grade II; ongoing urinary tract infections; use of anticholinergic drugs; calcium antagonists, beta-antagonists, and dopamine antagonists; those who do not sign the Informed Consent Term.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Decreased frequency and volume of urinary loss in women with urinary incontinence, evaluated by ICIQ-OAB, ICIQ-SF, ISI and OAB-V8 questionnaries and the Uninary Diary, through the observation of a variation of at least 5% in the pre and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement of the quality of life of the study participants evaluated through the ICIQ-SF, ICIQ-OAB, OAB-V8 and ISI questionnaires, through the observation of a variation of at least 5% in the pre and post-intervention measurements. | — |
Countries
Brazil
Contacts
Public ContactCristiane;Raissa Pedroni;Avramidis
Universidade Estadual Paulista;Universidade Estadual Paulista
Outcome results
None listed