Urinary incontinence
Conditions
Interventions
The study sample will be composed of 408 puerperae. These will be randomized into a control group (N: 204) who will receive the routine care of the participating institutions and the intervention grou
L01.224.900.685
G11.427.410.698.277
Sponsors
Departameto de Enfermagem da Universidade Federal do Ceará
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Puerperas of physiological vaginal birth to term; over 18 years; with mobile phone or similar compatible with the application
Exclusion criteria
Exclusion criteria: Women with urinary incontinence or pelvic organ prolapse; gynecological surgeries for correction of previous pelvic floor dysfunctions; pelvic radiotherapy; collagen diseases; apparent mental state that makes collection impossible
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint will be the prevalence of urinary incontinence three months after delivery by self-report of participants | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes will be knowledge, attitude and practice of puerperal women on urinary incontinence three months after the intervention; adherence to the muscular training program and motivation, satisfaction and mastery over the application in the women in the intervention group | — |
Countries
Brazil
Contacts
Public ContactCamila Moreira Vasconcelos
Departameto de Enfermagem da Universidade Federal do Ceará
Outcome results
None listed