stress urinary incontinence
Conditions
Interventions
In the experimental group, comprising 35 women, training to correctly perform the movement guide the intervention for dynamic lumbopelvic stabilization. The movements used in the evaluation now will e
b) 20 contractions maintained for 2 seconds with equal rest time between them
c) 20 contractions maintained for 1 second with equal rest time between them
d) 5 contractions maintained for 10 seconds with equal rest time between them
e) 5 repetitions of strong contractions associated with cough with 1 minute intervals between each contraction and will have lasting approximately 15 minutes. All exercises should be done in the supin
Other
E02.779.483
Sponsors
Faculdade de Medicina - UFJF
Universidade Federal de Juiz de Fora
Faculdade de Medicina - UFJF
Eligibility
Sex/Gender
Female
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: literate women aged greater than or equal to 18 years with reports of efforts to urinary losses and sexually active
Exclusion criteria
Exclusion criteria: Possessing dystopias grades III and IV or use of anticholinergic drugs, pregnant women, women in treatment for urinary incontinence, pelvic diaphragm dysfunction or changes the alignment of the spine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome: reduction of urinary leakage measured by incontinence severity index and voiding diary in both groups, but more significant from a statistical point of view in the experimental group, calculated by the size of the effect (calculated by eta squared and the d Cohen) . The significance level was 5% (p ? 0.05).;Outcome found: reduction of urinary losses similar groups in post treatment. However, only the experimental group this improvement remained in the evaluation 90 days after intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome: improved sexual performance verified by sex ratio, female version, and the quality of life measured by international consultation questionnaires on incontinence questionnaire and King's Health Questionnaire in both groups, but more significant from a statistical point of view the experimental group. The calculation will be done by the effect size (calculated by eta squared and the d Cohen). The significance level was 5% (p ? 0.05).;Outcome found: improved quality of life, particularly the experimental group, which remained in the evaluation 90 days after treatment. There was no statistical significance for sexual function in either group. | — |
Countries
Brazil
Contacts
Public ContactNathalia Abreu Freire
Universidade Federal de Juiz de Fora
Outcome results
None listed