Unspecified urinary incontinence
Conditions
Interventions
This is a randomized, controlled, blinded clinical trial. Intervention Group (IC): 22 women selected, randomized by a blinded researcher, who present at least 2 cm of diastasis of the rectus abdominis
G11.427.410.698.277
Sponsors
Universidade Federal de Uberlândia
Universidade Federal de Uberlândia
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Will be included women aged 18 or over; between 45 days and six months postpartum; with diagnosis of diastasis, considered as from 2 cm of distance at a point of the extension of the linea alba, no history of previous abdominal aesthetic surgeries; do not have musculoskeletal disease that makes it impossible to perform the requested exercises.
Exclusion criteria
Exclusion criteria: Women who miss 20% of the intervention or do not show up for evaluation; women diagnosed with midline abdominal hernia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The hypopressive training method is expected to approach 5% of the borders of the rectus abdominis at one of the diastasis points along the linea alba assessed by imaging ultrasound. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that the hypopressive training method will improve abdominal function by 5%, assessed by the plank test, in addition to improving the pelvic floor complaints by 5% of the Pelvic Floor Questionnaire scores. | — |
Countries
Brazil
Contacts
Public ContactSara Moreira
Universidade Federal de Uberlândia
Outcome results
None listed