None listed
Conditions
Interventions
The volunteers will be randomly distributed in two groups: group 1 will be treated with medium frequency current - 2000Hz of frequency, 100 microseconds of pulse width, 4:8 seconds of on:off - and group 2 with low frequency current - 50Hz of frequency, 700 microseconds of pulse width, 4:8 seconds of on:off (neuromuscular electrical stimulation using vaginal electrodes). The duration of each session was 20 minute twice per week during six weeks.
Sponsors
Elaine Caldeira De Oliveira Guirro
Study design
Allocation
Randomised controlled trial
Primary purpose
Treatment
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
stress urinary incontinence and female gender
Exclusion criteria
Pelvic organ prolapse; pregnancy; vaginal and/or urinary tract infection; present history of urogynecologic surgery in the last 6 months; pacemaker; instability of detrusor muscle; intrinsic sphincter deficiency; hormonal replacement therapy.
Outcome results
None listed